Abstract
Besides the main cortical inputs to the basal ganglia, via the corticostriatal projection, there is another input via the corticosubthalamic projection (CSTP), terminating in the subthalamic nucleus (STN). The present study investigated and compared the CSTPs originating from the premotor cortex (PM) or the primary motor cortex (M1) in two groups of adult macaque monkeys. The first group includes six intact monkeys, whereas the second group was made up of four monkeys subjected to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) intoxication producing Parkinson’s disease (PD)-like symptoms and subsequently treated with an autologous neural cell ecosystem (ANCE) therapy. The CSTPs were labeled with the anterograde tracer biotinylated dextran amine (BDA), injected either in PM or in M1. BDA-labeled axonal terminal boutons in STN were charted, counted, and then normalized based on the number of labeled corticospinal axons in each monkey. In intact monkeys, the CSTP from PM was denser than that originating from M1. In two PD monkeys, the CSTP originating from PM or M1 were substantially increased, as compared to intact monkeys. In one other PD monkey, there was no obvious change, whereas the last PD monkey showed a decrease of the CSTP originating from M1. Interestingly, the linear relationship between CSTP density and PD symptoms yielded a possible dependence of the CSTP re-organization with the severity of the MPTP lesion. The higher the PD symptoms, the larger the CSTP densities, irrespective of the origin (from both M1 or PM). Plasticity of the CSTP in PD monkeys may be related to PD itself and/or to the ANCE treatment.
Introduction
In parallel to the multiple descending motor pathways originating from cortical areas, such as the corticospinal (CST), the corticorubral, corticotectal, and the corticobulbar (corticoreticular) projections (Lemon, 2008), motor control is also based on cortico-basal ganglia circuit loops. The majority of motor cortical inputs to the basal ganglia are directed to the striatum (e.g., Künzle, ; McGuire et al., ; Inase et al., , ; Takada et al., ,; Tokuno et al., ; Nambu et al., ; Tachibana et al., ; Parent and Parent, ; Raju et al., ; Gerbella et al., ; Innocenti et al., ). However, other cortical projections to the basal ganglia reach the subthalamic nucleus (STN), via corticosubthalamic projections (CSTPs) originating from the primary motor cortex (M1), the supplementary motor areas (SMA-proper and pre-SMA), the premotor cortex (PM), and the cingulate motor areas, representing a hyper direct pathway parallel to the classic direct and indirect pathways (Nambu et al., , , , ; Inase et al., ; Takada et al., ; Miyachi et al., ; Degos et al., ; Inoue et al., ; Iwamuro et al., ; Coudé et al., ; Temiz et al., ).
Based on the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) intoxication model, producing Parkinson’s disease (PD)-like symptomatic macaque monkeys, it was shown that a cellular therapy referred to as autologous neural cell ecosystem (ANCE) improves recovery of motor control (Bloch et al., ; Borgognon et al., , ). Subsequently, in four of such MPTP intoxicated monkeys subjected to ANCE therapy, tracing studies showed that the corticobulbar (corticoreticular) projections were significantly reduced as compared to intact monkeys (Fregosi et al., ), whereas the corticotectal projection was much less affected (Fregosi et al., ). As far as the corticosubthalamic projection (CSTP) is concerned, a loss of the hyper direct pathway was reported in PD mice (Chu et al., ). Similarly, the cortical innervation of the STN was reduced in PD monkeys (Mathai et al., ). In the latter two studies, the evidence for a reduction of cortical inputs to STN was derived from immunohistochemical detection of vesicular glutamate transporter type-1 terminals, making it impossible to discriminate the distinct origins of the CSTP inputs, for example, M1 vs. PM.
Our goal then was to investigate in 10 adult macaque monkeys how CSTPs originating from PM and M1 are affected by PD-like symptoms, by comparing a group of six intact monkeys with another group of four PD monkeys treated with ANCE. Each group of monkeys was split into two, half of the animals injected with the anterograde tracer biotinylated dextran amine (BDA) in PM and the other half receiving the same injection in M1. It was hypothesized that PD and the subsequent recovery following ANCE treatment, would result in a modification of the density of the CSTP when compared to intact monkeys. Subsequently, the group of intact monkeys was used to investigate whether the density of the CSTP differs based on its origin, PM vs. M1.
Materials and Methods
All surgical experimental procedures, experiments, and animal care were conducted in respect to the ethical guidelines (ISBN 0-309-05377-3, 1996) and authorized by the local (Canton of Fribourg) and federal (Switzerland) veterinary authorities (authorizations No. 44_92_3; 150_00; 156_02; 156_08E; 2012_01-FR; 2012_01E_FR). The conditions of housing in the animal facility were described earlier in detail (Borgognon et al., , ; see also: http://www.unifr.ch/spccr/about/housing).
The materials and methods are similar to those reported in recent publications related to the corticobulbar (corticoreticular) and corticotectal projections (Fregosi and Rouiller, ; Fregosi et al., , , ). Briefly, surgeries were performed under sterile conditions in anesthetized animals. The protocol consisted of a unilateral cortical (PM or M1) injection of the anterograde tracer BDA (MW = 10,000; Molecular Probe, Eugene, OR, USA) using a 10 μl Hamilton micro-syringe. BDA concentration was 5% (in distilled water) for Mk-M93-80 and 10% for the other nine monkeys (see Table 1). The extent of the BDA injection was assessed on consecutive histological frontal sections, each reconstructed manually using Neurolucida software (MBF Bioscience-MicroBrightField Inc., version 11). Three-dimension (3D) reconstruction was performed by stacking on a dorsolateral view the medio-lateral extent of BDA intake from the midline. The injection sites in PM involved both PMd and PMv in most animals, except in Mk-R12 and Mk-LL in which BDA was delivered mostly in PMd. The BDA injection in M1 was limited to the hand area in Mk-93-80, as defined by intracortical microstimulation. For the other M1 injections, based on anatomical landmarks (cortical sulci), BDA involved the hand area, as well as more proximal territories of the forelimb (Figure 1). Although, some modest spread (so-called “halo”) in the PM injected animals could be observed, BDA in general did not exhibit extensive spread (Fregosi et al., , ; see Mk-CH; Mk-R13 and Mk-R12 in Figure 1). Using an exhaustive plotting method (perfectly suitable to the small size of the STN) with Neurolucida software, the axonal terminal boutons in the STN labeled with the anterograde tracer BDA were registered in each monkey, following unilateral BDA injection either in M1 or in PM. The BDA injections took place usually about 30 days before euthanasia. The same 10 monkeys involved in the present analysis (Table 1) were already used to establish the properties of the corticoreticular projection from M1 and PM in intact monkeys (Fregosi et al., ) and in PD monkeys (Fregosi et al., ), as well as the corresponding corticotectal projections (Fregosi and Rouiller, ; Fregosi et al., ).
Table 1
| BDA injection in PM | BDA injection in Ml | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Intact monkeys | MPTP monkeys | Intact monkeys | MPTP monkeys | |||||||
| Monkey’s ID | Mk-R12 | Mk-R13 | Mk-CH | Mk-MY | Mk-LL | Mk-M310 | Mk-Z182 | Mk-93-80 | Mk-MI | Mk-LY |
| Sex | female | female | male | female | female | male | male | male | female | female |
| Age at sacrifice (years) | 6 | 4.5 | 10 | 9.5 | 7.5 | 8.5 | 7.5 | 4 | 9.5 | 7.5 |
| Weight (kg) | 4 | 4 | 6 | 4.3 | 3.6 | 10 | 10 | 4 | 3.3 | 3.3 |
| BDA volume injected (μl) | 7.2 | 8.8 | 8 | 11.5 | 9.7 | 22.5 | 25.5 | 10.5 | 9 | 9 |
| Nb. of BDA injections sites | 9 | 11 | 10 | 9 | 8 | 15 | 17 | 7 | 6 | 6 |
| Loss of TH+ neurons in SNpc | - | - | - | −72% | −67% | - | - | - | −74% | −39% |
| Nb. of boutons (raw) | 1,395 | 1,722 | 788 | 1,466 | 434 | 109 | 127 | 684 | 541 | 25 |
| Inter-section distance (μm) | 250 | 250 | 250 | 500 | 500 | 400 | 400 | 350 | 500 | 500 |
| Sampling interval | 1/2 | 1/2 | 1/2 | all | all | all | all | 1/2 | all | all |
| Correction factor | 2 | 2 | 2 | 2 | 2 | 1.6 | 1.6 | 2.8 | 2 | 2 |
| Corrected nb. of boutons | 2,790 | 3,444 | 1,576 | 2,932 | 868 | 174 | 203 | 1,915 | 1,082 | 50 |
| Nb. of CST labeled axons | 1,473 | 1,802 | 1,201 | 611 | 593 | 703 | 950 | 3,195 | 1,117 | 1,671 |
| Norm and Corr. of boutons | 1,894 | 1,911 | 1,312 | 4,799 | 1,464 | 248 | 214 | 599 | 969 | 30 |
| MD perf. post-MPTP | - | - | - | 72% | 100%& | - | - | - | 13% | 100% |
| MD perf. post-ANCE | - | - | - | 95% | 100%& | - | - | - | 52% | 100% |
All monkeys were adult Macaca fascicularis.
All 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) monkeys were treated with autologous neural cell ecosystem (ANCE). The inter-section interval of 250 microns was taken as a reference to compute the correction factor (see “Materials and Methods” section). The number of biotinylated dextran amine (BDA)-labeled axonal boutons in subthalamic nucleus (STN) was corrected for other inter-sections intervals, as well as the sampling interval (all sections analysed or 1 out of 2 sections analyzed; see “Materials and Methods” section). Finally, the corrected number of axonal boutons in STN was normalized, based on the number of corticospinal axons labeled with BDA in the same monkey (see “Materials and Methods” section). The loss of TH+ neurons in the SNpc was expressed in % with respect to intact monkeys (see Borgognon et al., ). MD, Manual Dexterity; performance measured based on the Modified Brinkman Board, with reference to the performance pre-lesion (100%). See Borgognon et al. (). &For Mk-LL, the MD performance was hectic, preventing the calculation of reliable scores, although the deficit post MPTP lesion was rather modest or inexistent. Therefore, her MD performance was considered to be at 100% (see “Materials and Methods” section). Further individual data for these monkeys can be found in Fregosi and Rouiller (), Fregosi et al. (, , ), Badoud et al. () and Borgognon et al. (, ).
Figure 1
The six intact monkeys were restricted to tracing investigations, whereas the four PD monkeys were also included in behavioral, imaging, and histochemical assessments (Badoud et al., ; Borgognon et al., , ). The low-dose MPTP intoxication (see Mounayar et al., ) in the four PD monkeys as well as the ANCE transplantation have been previously described (Borgognon et al., , ). Briefly, the MPTP protocol consisted of a series of daily intramuscular injections (Sigma–Aldrich Company; 0.5 mg/kg, dissolved in saline solution) until the monkeys reached an adequate level of motor impairment as assessed by the Schneider MPTP scale (Schneider et al., ). During the MPTP intoxication protocol, a dorsolateral prefrontal cortex biopsy was performed to obtain the necessary cellular material (Badoud et al., ). Then, the cortical samples were immediately processed to be put into the culture to obtain the ANCE. After the post-MPTP lesion plateau (about 6 weeks after the last MPTP injection), the ANCE were implanted in six striatal regions: one in the caudate nucleus and two in the putamen for both hemispheres. All four animals were trained to perform two fine manual dexterity tasks: (1) the modified-Brinkman board task, where the animal retrieved a food pellet using a precision grip (opposition thumb and index finger); and (2) the reach and grasp drawer task, where the monkey pulled-open a drawer to retrieve a reward using a precision grip. During the entire experimental protocol, all four animals were tested pre-post-MPTP lesion and post-ANCE transplantation.
The STN boundary was delineated using a series of 50 μm Nissl stained, frontal sections (at a total magnification of 12.5×), whereas the STN was scanned on a second (adjacent) series of sections processed for BDA, to chart and count the number of terminal or en passant axonal boutons (at a total magnification of 200×). The Nissl stained and the BDA sections were then superimposed, showing the spatial distribution of the axonal boutons in the STN (Figure 2). The size of the STN boutons was very small (below 1 μm in diameter) therefore forming a homogeneous population across all the animals. This is in contrast to the boutons observed in the different corticofugal projections, that exhibited various diameters (Fregosi and Rouiller, ; Fregosi et al., , , ). To account for various inter-section distances across animals and the analyzed number of sections of the BDA series, the raw numbers of boutons in each monkey were corrected by multiplying it by a correction factor, f:
where d is the inter-section distance in μm; R is the reference (250 μm for all the animals) and s is the sampling interval (=0.5 if only one out of two sections were analyzed; or = 1 if all the sections were analyzed; Table 1). Finally, to compensate for variations in the size and location of the BDA injection sites, as well as differences in tracer uptake, the corrected numbers of boutons were divided by the number of corticospinal axons labeled just above the pyramidal decussation and multiplied by 1,000 to keep a realistic normalized number of boutons (Table 1). The normalization procedure has been described in detail earlier (Fregosi and Rouiller, ; Fregosi et al., , , ). Representation of the BDA injection sites in the 10 monkeys was published previously (Fregosi et al., , ).
Figure 2
Due to the low number of animals we performed a bootstrapping analysis (MATLAB R2017b), where the initial population of n analyzed histological sections, covering the rostrocaudal extent of the STN, was resampled with replacement to obtain k = 100,000 fictive populations of n sections independently for each animal. For each bootstrapped population, we summed up the number of BDA-labeled boutons along the rostrocaudal axis to finally obtain the total number of BDA-labeled boutons of the 100,000 bootstrapped populations. As standard in bootstrapping, we calculated the p-value by estimating the residuals of the combined distribution testing for the null hypothesis that the gaussian distribution of the difference had a mean value of 0:
where N is the gaussian distribution function; μ1 and μ2 are the means of the two conditions with μ1 > μ2 and σ1 and σ2 are their respective standard deviations. Finally, the significance threshold of the p-value has been adjusted using the Bonferroni correction for multiple-group comparisons (α = 0.05 divided by the number of groups).
To assess the relationship between the number of BDA-labeled boutons with the interaction between motor impairment (PD symptoms based on manual dexterity in the modified-Brinkman board task post-ANCE transplantation (see above) and dopaminergic (tyrosine hydroxylase positive (TH+) neurons) loss in the substantia nigra pars compacta (SNpc), we performed a multivariable linear regression model test (MATLAB R2017b, function “fitlm”; Contestabile et al., ). To have a comparable (and reasonable amount of) variables between M1 and PM, the number of BDA-labeled boutons were normalized by dividing each variable by the maximum number of BDA-labeled boutons for M1 and PM, respectively. Note, that Mk-LL showed no PD symptoms in the clinical score (Borgognon et al., ) and in the reach and grasp drawer task (Borgognon et al., ). Therefore, we considered Mk-LL being at 100% of its motor performance although she had a hectic behavior in the modified-Brinkman board task (Table 1).
Results
Following unilateral BDA injection in M1 or PM, labeled axons were visible in the homolateral internal capsule (mostly CST axons), together with a dark labeled axonal terminal field in STN (Figure 2Ai). At high magnification, the axonal terminal field contains identifiable axonal boutons (arrows, Figure 2Aii). The boutons were defined as a swelling of the axon branch, corresponding to at least a 2-fold increase in axon diameter (Fregosi and Rouiller, ; Fregosi et al., , , ). As shown in the Figure 2A for Mk-MY (MPTP intoxicated; BDA injected in PM), the BDA-labeled axonal boutons were located in specific subregions of the STN, whose position varied along the rostrocaudal axis. A comparable distribution of BDA-labeled axonal boutons is shown for two other representative monkeys, one MPTP intoxicated (Mk-MI; BDA injected in M1) and an intact animal (Mk-CH; BDA injected in PM; Figures 2B,C).
As shown in Figure 2A, the axonal boutons in STN were all tiny and smaller than axonal boutons observed in the ponto-medullary reticular formation (Fregosi et al., , ) or in the superior colliculus (Fregosi and Rouiller, ; Fregosi et al., ). Indeed, the very small axonal boutons in STN were at the opposite extrema of the giant endings formed by another corticofugal projection originating in layer V, and terminating in the thalamus (e.g., Rouiller et al., , ; Rouiller and Welker, ). As observed previously for the corticoreticular (Fregosi et al., , ) and the corticotectal projections (Fregosi and Rouiller, ; Fregosi et al., ), in the STN the axonal boutons en passant were far more numerous than the boutons terminaux, although they could not always reliably distinguished, as previously reported (Fregosi et al., ).
The numbers of BDA-labeled axonal boutons over the sections covering the STN were then corrected, normalized, and finally bootstrapped, see “Materials and Methods” section. The final bootstrapped numbers of axonal boutons are shown in Figure 3 for monkeys injected with BDA in PM (blue) or in M1 (green). In each of the two subgroups of intact monkeys (PM or M1 injections), the three animals yielded comparable numbers of normalized axonal boutons in STN (statistically non-significant; p > 0.0083). However, the density of the CSTPs from PM was higher than those from M1 (p < 0.0083) in all two by two inter-animal comparisons, except Mk93-80 compared to Mk-CH (p = 0.0104).
Figure 3
The inter-individual variability of the numbers of BDA-labeled axonal boutons in STN was larger in the PD monkeys than in intact monkeys, although again in the PD monkeys the projection from PM was stronger than from M1 (Table 1). More specifically, as a result of BDA injection in M1, one PD monkey (Mk-LY) exhibited a lower number of labeled axonal boutons in STN (Table 1, Figure 4C; p < 0.0125 except compared with Mk-93-80, where p = 0.0198). Mk-LY was characterized by a modest loss of TH+ neurons in the SNpc (−39%), and a complete spontaneous functional recovery (see Borgognon et al., ). The second PD monkey (Mk-MI; subjected to BDA injection in M1) exhibited about twice the number of labeled axonal boutons in STN, as compared to the three intact animals (Table 1), although the bootstrap analysis showed a significant difference only in animal Mk-Z182 (Figure 4D, p = 0.0075). Mk-MI was characterized by a significant loss of dopaminergic neurons in SNpc (−74%) and severe PD symptoms. In the two PD monkeys subjected to BDA injection in PM, one animal (Mk-LL, −67% of TH+ neuronal loss) had numbers of labeled axonal boutons in STN that were comparable to intact animals (Figure 4A, p > 0.0125), whereas the second monkey (Mk-MY, −72% of TH+ neuronal loss) showed a dramatically higher number of axonal boutons in STN (Figure 4B, p < 0.0125).
Figure 4
Predictably, the summary of the multivariable linear regression model showed a significant interaction between TH+ loss in SNpc and motor impairment (Table 2, p = 0.015). To visualize the fit of the dependent variables (number of boutons) against the independent variables (TH+ loss and PD symptoms), all the variables were “partialed-out” except for the constant term. The model showed an explanatory power (positive slope: y = 9.298*x). If it did not, it would appear as a horizontal line (Figure 5). Moreover, the model showed a positive correlation between the number of BDA-labeled boutons with the loss of TH+ neurons in SNpc and the motor impairment (root mean squared error = 0.169; R2 = 0.821, adjusted R2 = 0.731, p-value = 0.0117). The four PD monkeys were clustered in two different spaces compared to the intact group. Indeed, the two PD animals (Mk-LY and Mk-LL) with less TH+ loss and the lowest motor impairment, were located at the bottom left of the graph (purple cluster), whereas the two PD animals (Mk-MY and Mk-MI) with more TH+ loss and greater motor impairment were on the top right of the graph (yellow cluster).
Table 2
| Estimate | SE | tStat | p-value | |
|---|---|---|---|---|
| Intercept | 554.45 | 163.72 | 3.387 | 0.015 |
| TH+ loss in SNpc | −7.47 | 2.21 | −3.377 | 0.015 |
| PD symptoms | −5.54 | 1.63 | −3.385 | 0.015 |
| TH+ loss : PD symptoms | 0.07 | 0.02 | 3.378 | 0.015 |
Estimated coefficients of the linear regression model.
Figure 5
Discussion
Although the topography of the CSTPs from M1 and PM in macaques has been established previously (Nambu et al., ), the originality of the present study is to provide new evidence that the projection from PM to STN is denser than that from M1 to STN, after normalization, based on the number of labeled CST axons. Recently, Coudé and colleagues have shown that the innervation of the STN arises from the collaterals of long-range corticofugal axons en route to lower brainstem regions. In our analysis, we used the numbers of CST axons to normalize the data, which could bias the results if CST neurons emit collaterals to the STN. However, the bias would be in favor of M1 projections (more boutons from M1 than PM) because ~50% of CST neurons originate from M1 as opposed to only ~10–20% from PM (Dum and Strick, ). A similar difference between PM and M1 was found for the corticoreticular projection (Fregosi et al., ), as well as the corticotectal projection (Fregosi and Rouiller, ). In other words, in the sense of a tentative generalization, it seems that PM is in a position to exert a stronger influence on subcortical relays (STN, ponto-medullary reticular formation, superior colliculus) than M1. As far as the topography of the axonal terminal field in STN is concerned, the present data are largely consistent with the study of Nambu et al. ().
The quantitative data of the present study depend strongly on the normalization procedure based on the number of BDA-labeled CST axons in the same monkeys. The pros and cons of such normalization were discussed in detail earlier (Fregosi and Rouiller, ; Fregosi et al., , , ). The rationale for such normalization is to compensate for variability in tracer uptake and injection site sizes. In particular, to take into account variations in the laminar spread of BDA in the injected area, with the consideration that layer V is the most relevant to the investigation of corticofugal projections to the basal ganglia, the ponto-medullary reticular formation, or the superior colliculus (Gerfen et al., ). The number of CST axons can easily be counted above the pyramidal decussation and as the CST axons also originate from layer V, it may be an adequate normalizing factor to compensate for interindividual differences in terms of BDA spread in layer V.
The present data suggest that the CSTP is increased in PD monkeys subjected to the ANCE treatment, although this observation is restricted to two out of four animals. The limitation here is of course the interindividual variability among the PD monkeys, as well as the low number of cases, which is, however, often the case in non-human primate studies for ethical reasons. Obviously, the present pilot study needs to be extended with more monkeys (intact and PD), especially PD monkeys without ANCE treatment (see below). The increase of the CSTP in the two PD monkeys (Mk-MY and Mk-MI) is in apparent contradiction with previous reports of a reduction of the cortical innervation of the STN in PD monkeys (Mathai et al., ) and in PD mice (Chu et al., ). The discrepancy may result from the fact that the present PD monkeys were treated with ANCE, whereas there were no treatments in the other two studies (Mathai et al., ; Chu et al., ). However, the two PD monkeys with less dopaminergic neuronal loss and low motor impairment (Mk-LY and Mk-LL, purple cluster) are more in concordance with the two previous studies (Mathai et al., ; Chu et al., ). Indeed, Mk-LY showed a dramatic decrease in the CSTP from M1, whereas Mk-LL exhibited comparable CSTP from PM. Overall, the linear model may suggest that the re-organization of the CSTP depends on both the PD symptoms and the dopaminergic loss in SNpc. Again, future experiments are needed in PD monkeys subjected to BDA injections in PM or M1, but in absence of ANCE treatment, with the hypothesis that the CSTP may decrease from M1 and remain stable from PM, as compared to intact monkeys. Furthermore, the readout for axon terminals in STN was not the same across studies (Mathai et al., ; Chu et al., vs. present study; see “Introduction” section). In the same four PD monkeys treated with ANCE, the corticoreticular projection was reduced as compared to intact monkeys (Fregosi et al., ). The present study suggests changes in the CSTP in cases with PD-like symptoms in ANCE treated monkeys, although, with individual variability, it is consistent with the notion that the STN is a major target for the reduction of PD symptoms, as has been demonstrated in MPTP monkeys (e.g., Benazzouz et al., ; Guridi et al., , ).
The increase of the CSTPs observed in two out of four PD monkeys, when compared to the percentage of loss of dopaminergic neurons (TH+ neurons) in the SNpc, may be indicative of a threshold effect. Indeed, it is known that stable PD symptoms remain present after MPTP intoxication only when a threshold is reached for the loss of dopaminergic neurons in SNpc (see e.g., Soderstrom et al., ; Borgognon et al., ). In the present report, the increase of CSTPs was observed in the two PD monkeys with a greater than 70% loss of dopaminergic neurons (Mk-MY and Mk-MI), whereas in the other two PD monkeys the dopaminergic neurons’ loss was lower than 70%. A tentative (and speculative) threshold at 70% for an effect on the CSTP would be consistent with the behavioral observation that the monkeys Mk-MY and Mk-MI exhibited stronger and more stable motor deficits after MPTP lesion, and before ANCE treatment, than the other two PD monkeys (Borgognon et al., , ).
Statements
Data availability statement
On request, access can be provided to the histological sections (contact the corresponding author).
Ethics statement
The animal study was reviewed and approved by Service de la sécurité alimentaire et des affaires vétérinaires SAAV Amt für Lebensmittelsicherheit und Veterinärwesen LSVW.
Author contributions
EMR designed the tracing experiments. EMR analyzed the histological sections. SBo performed the multivariable linear model and the bootstrapping analysis. SBa, JC, EMR and SBo designed and performed the MPTP experiments. JB and J-FB designed the ANCE treatment. EMR and SBo drafted the manuscript. All authors contributed to the article and approved the submitted version.
Funding
The present study was financially supported by Swiss National Science Foundation (SNF) grants to EMR, numbers 110005, 132465, 144990, and 149643; grant Sinergia SNF PROMETHEUS number CRSI33_125408; grant Sinergia SNF number CRSII3_160696; and the Swiss Primate Competence Centre for Research (SPCCR: http://www.unifr.ch/spccr).
Acknowledgments
We thank Mrs. Christine Roulin, Christiane Marti, Véronique Moret for their technical precious contributions to process the histological tissue, the animal caretakers (L. Bossy, J. Maillard, B. Bapst, B. Morandi, and J. Corpataux), Dr. Michael Harvey for the proof-reading as well as Prof. Marco Capogrosso and Marion Badi for their help in the bootstrapping analysis.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
- CSTP
corticosubthalamic projection
- BDA
biotinylated dextran amine
- CST
corticospinal
- MPTP
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine
- PD
Parkinson-like symptoms
- M1
Primary motor cortex
- PM
Premotor cortex
- SNpc
substantia nigra pars compacta
- STN
subthalamic nucleus
- ANCE
autologous neural cell ecosystem.
Abbreviations
References
1
BadoudS.BorgognonS.CottetJ.ChatagnyP.MoretV.FregosiM.et al. (2017). Effects of dorsolateral prefrontal cortex lesion on motor habit and performance assessed with manual grasping and control of force in macaque monkeys. Brain Struct. Funct.222, 1193–1206. 10.1007/s00429-016-1268-z
2
BenazzouzA.GrossC.FegerJ.BoraudT.BioulacB. (1993). Reversal of rigidity and improvement in motor performance by subthalamic high-frequency stimulation in MPTP-treated monkeys. Eur. J. Neurosci.5, 382–389. 10.1111/j.1460-9568.1993.tb00505.x
3
BlochJ.BrunetJ. F.McEntireC. R.RedmondD. E. (2014). Primate adult brain cell autotransplantation produces behavioral and biological recovery in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonian St. Kitts monkeys. J. Comp. Neurol.522, 2729–2740. 10.1002/cne.23579
4
BorgognonS.CottetJ.MoretV.ChatagnyP.CarraraL.FregosiM.et al. (2019). Fine manual dexterity assessment after autologous neural cell ecosystem (ANCE) transplantation in a non-human primate model of Parkinson’s disease. Neurorehabil. Neural Repair33, 553–567. 10.1177/1545968319850133
5
BorgognonS.CottetJ.MoretV.ChatagnyP.GinovartN.AntonescuC.et al. (2017). Enhancement of striatal dopaminergic function following autologous neural cell ecosystems (ANCE) transplantation in a non-human primate model of Parkinson’s disease. J. Alzheimers Dis. Parkinsonism7, 1–11. 10.4172/2161-0460.1000383
6
ChuH. Y.McIverE. L.KovaleskiR. F.AthertonJ. F.BevanM. D. (2017). Loss of hyperdirect pathway cortico-subthalamic inputs following degeneration of midbrain dopamine neurons. Neuron95, 1306–1318. 10.1016/j.neuron.2017.08.038
7
ContestabileA.ColangiuloR.LucchiniM.GindratA. D.HamadjidaA.KaeserM.et al. (2018). Asymmetric and distant effects of a unilateral lesion of the primary motor cortex on the bilateral supplementary motor areas in adult macaque monkeys. J. Neurosci.38, 10644–10656. 10.1523/JNEUROSCI.0904-18.2018
8
CoudéD.ParentA.ParentM. (2018). Single-axon tracing of the corticosubthalamic hyperdirect pathway in primates. Brain Struct. Funct.223, 3959–3973. 10.1007/s00429-018-1726-x
9
DegosB.DeniauJ. M.LeC. J.MaillyP.MauriceN. (2008). Evidence for a direct subthalamo-cortical loop circuit in the rat. Eur. J. Neurosci.27, 2599–2610. 10.1111/j.1460-9568.2008.06229.x
10
DumR. P.StrickP. L. (1991). The origin of corticospinal projections from the premotor areas in the frontal lobe. J. Neurosci.11, 667–689. 10.1523/JNEUROSCI.11-03-00667.1991
11
FregosiM.ContestabileA.BadoudS.BorgognonS.CottetJ.BrunetJ. F.et al. (2018). Changes of motor corticobulbar projections following different lesion types affecting the central nervous system in adult macaque monkeys. Eur. J. Neurosci.48, 2050–2070. 10.1111/ejn.14074
12
FregosiM.ContestabileA.BadoudS.BorgognonS.CottetJ.BrunetJ. F.et al. (2019). Corticotectal projections from the premotor or primary motor cortex after cortical lesion or parkinsonian symptoms in adult macaque monkeys: a pilot tracing study. Front. Neuroanat.13:50. 10.3389/fnana.2019.00050
13
FregosiM.ContestabileA.HamadjidaA.RouillerE. M. (2017). Corticobulbar projections from distinct motor cortical areas to the reticular formation in macaque monkeys. Eur. J. Neurosci.45, 1379–1395. 10.1111/ejn.13576
14
FregosiM.RouillerE. M. (2017). Ipsilateral corticotectal projections from the primary, premotor and supplementary motor cortical areas in adult macaque monkeys: a quantitative anterograde tracing study. Eur. J. Neurosci.46, 2406–2415. 10.1111/ejn.13709
15
GerbellaM.BorraE.MangiaracinaC.RozziS.LuppinoG. (2016). Corticostriate projections from areas of the “lateral grasping network”: evidence for multiple hand-related input channels. Cereb. Cortex26, 3096–3115. 10.1093/cercor/bhv135
16
GerfenC. R.EconomoM. N.ChandrashekarJ. (2018). Long distance projections of cortical pyramidal neurons. J. Neurosci. Res.96, 1467–1475. 10.1002/jnr.23978
17
GuridiJ.HerreroM. T.LuquinM. R.GuillenJ.RubergM.LagunaJ.et al. (1996). Subthalamotomy in Parkinsonian monkeys -behavioural and biochemical analysis. Brain119, 1717–1727. 10.1093/brain/119.5.1717
18
GuridiJ.HerreroM. T.LuquinR.GuillenJ.ObesoJ. A. (1994). Subthalamotomy improves MPTP-induced parkinsonism in monkeys. Stereotact. Funct. Neurosurg.62, 98–102. 10.1159/000098603
19
InaseM.SakaiS. T.TanjiJ. (1996). Overlapping corticostriatal projections from the supplementary motor area and the primary motor cortex in the macaque monkey: an anterograde double labeling study. J. Comp. Neurol.373, 283–296. 10.1002/(sici)1096-9861(19960916)373:2<283::aid-cne10>3.0.co;2-m
20
InaseM.TokunoH.NambuA.AkazawaT.TakadaM. (1999). Corticostriatal and corticosubthalamic input zones from the presupplementary motor area in the macaque monkey: comparison with the input zones from the supplementary motor area. Brain Res.833, 191–201. 10.1016/s0006-8993(99)01531-0
21
InnocentiG. M.DyrbyT. B.AndersenK. W.RouillerE. M.CaminitiR. (2017). The crossed projection to the striatum in two species of monkey and in humans: behavioral and evolutionary significance. Cereb. Cortex27, 3217–3230. 10.1093/cercor/bhw161
22
InoueK.KoketsuD.KatoS.KobayashiK.NambuA.TakadaM. (2012). Immunotoxin-mediated tract targeting in the primate brain: selective elimination of the cortico-subthalamic “hyperdirect” pathway. PLoS One7:e39149. 10.1371/journal.pone.0039149
23
IwamuroH.TachibanaY.UgawaY.SaitoN.NambuA. (2017). Information processing from the motor cortices to the subthalamic nucleus and globus pallidus and their somatotopic organizations revealed electrophysiologically in monkeys. Eur. J. Neurosci.46, 2684–2701. 10.1111/ejn.13738
24
KünzleH. (1975). Bilateral projections from precentral motor cortex to the putamen and other parts of the basal ganglia. An autoradiographic study in Macaca fascicularis. Brain Res.88, 195–209. 10.1016/0006-8993(75)90384-4
25
LemonR. N. (2008). Descending pathways in motor control. Annu. Rev. Neurosci.31, 195–218. 10.1146/annurev.neuro.31.060407.125547
26
MathaiA.MaY.PareJ. F.VillalbaR. M.WichmannT.SmithY. (2015). Reduced cortical innervation of the subthalamic nucleus in MPTP-treated parkinsonian monkeys. Brain138, 946–962. 10.1093/brain/awv018
27
McGuireP. K.BatesJ. F.Goldman-RakicP. S. (1991). Interhemispheric integration: II. Symmetry and convergence of the corticostriatal projections of the left and the right pricipal sulcus (PS) and the left and the right supplementary motor area (SMA) of the rhesus monkey. Cereb. Cortex1, 408–417. 10.1093/cercor/1.5.408
28
MiyachiS.LuX.ImanishiM.SawadaK.NambuA.TakadaM. (2006). Somatotopically arranged inputs from putamen and subthalamic nucleus to primary motor cortex. Neurosci. Res.56, 300–308. 10.1016/j.neures.2006.07.012
29
MounayarS.BouletS.TandeD.JanC.PessiglioneM.HirschE. C.et al. (2007). A new model to study compensatory mechanisms in MPTP-treated monkeys exhibiting recovery. Brain130, 2898–2914. 10.1093/brain/awm208
30
NambuA.KanedaK.TokunoH.TakadaM. (2002a). Organization of corticostriatal motor inputs in monkey putamen. J. Neurophysiol.88, 1830–1842. 10.1152/jn.2002.88.4.1830
31
NambuA.TokunoH.TakadaM. (2002b). Functional significance of the cortico-subthalamo-pallidal ‘hyperdirect’ pathway. Neurosci. Res.43, 111–117. 10.1016/s0168-0102(02)00027-5
32
NambuA.TakadaM.InaseM.TokunoH. (1996). Dual somatotopical representations in the primate subthalamic nucleus: evidence for ordered but reversed body-map transformations from the primary motor cortex and the supplementary motor area. J. Neurosci.16, 2671–2683. 10.1523/JNEUROSCI.16-08-02671.1996
33
NambuA.TokunoH.HamadaI.KitaH.ImanishiM.AkazawaT.et al. (2000). Excitatory cortical inputs to pallidal neurons via the subthalamic nucleus in the monkey. J. Neurophysiol.84, 289–300. 10.1152/jn.2000.84.1.289
34
NambuA.TokunoH.InaseM.TakadaM. (1997). Corticosubthalamic input zones from forelimb representations of the dorsal and ventral divisions of the premotor cortex in the macaque monkey: comparison with the input zones from the primary motor cortex and the supplementary motor area. Neurosci. Lett.239, 13–16. 10.1016/s0304-3940(97)00877-x
35
ParentM.ParentA. (2006). Single-axon tracing study of corticostriatal projections arising from primary motor cortex in primates. J. Comp. Neurol.496, 202–213. 10.1002/cne.20925
36
RajuD. V.AhernT. H.ShahD. J.WrightT. M.StandaertD. G.HallR. A.et al. (2008). Differential synaptic plasticity of the corticostriatal and thalamostriatal systems in an MPTP-treated monkey model of parkinsonism. Eur. J. Neurosci.27, 1647–1658. 10.1111/j.1460-9568.2008.06136.x
37
RouillerE. M.TannéJ.MoretV.KermadiI.BoussaoudD.WelkerE. (1998). Dual morphology and topography of the corticothalamic terminals originating from the primary, supplementary motor, and dorsal premotor cortical areas in macaque monkeys. J. Comp. Neurol.396, 169–185. 10.1002/(sici)1096-9861(19980629)396:2<169::aid-cne3>3.0.co;2-z
38
RouillerE. M.WannierT.MorelA. (2003). The dual pattern of corticothalamic projection of the premotor cortex in macaque monkeys. Thalamus Relat. Syst.2, 189–197. 10.1017/s1472928803000190
39
RouillerE. M.WelkerE. (2000). A comparative analysis of the morphology of corticothalamic projections in mammals. Brain Res. Bull.53, 727–741. 10.1016/s0361-9230(00)00364-6
40
SchneiderJ. S.LidskyT. I.HawksT.MazziottaJ. C.HoffmanJ. M. (1995). Differential recovery of volitional motor function, lateralized cognitive function, dopamine agonist-induced rotation and dopaminergic parameters in monkeys made hemi-Parkinsonian by intracarotid MPTP infusion. Brain Res.672, 112–127. 10.1016/0006-8993(94)01332-c
41
SoderstromK.O’MalleyJ.Steece-CollierK.KordowerJ. H. (2006). Neural repair strategies for Parkinson’s disease: insights from primate models. Cell Transplant.15, 251–265. 10.3727/000000006783982025
42
TachibanaY.NambuA.HatanakaN.MiyachiS.TakadaM. (2004). Input-output organization of the rostral part of the dorsal premotor cortex, with special reference to its corticostriatal projection. Neurosci. Res.48, 45–57. 10.1016/j.neures.2003.09.006
43
TakadaM.TokunoH.HamadaI.InaseM.ItoY.ImanishiM.et al. (2001). Organization of inputs from cingulate motor areas to basal ganglia in macaque monkey. Eur. J. Neurosci.14, 1633–1650. 10.1046/j.0953-816x.2001.01789.x
44
TakadaM.TokunoH.NambuA.InaseM. (1998a). Corticostriatal input zones from the supplementary motor area overlap those from the contra-rather than ipsilateral primary motor cortex. Brain Res.791, 335–340. 10.1016/s0006-8993(98)00198-x
45
TakadaM.TokunoH.NambuA.InaseM. (1998b). Corticostriatal projections from the somatic motor areas of the frontal cortex in the macaque monkey: segregation versus overlap of input zones from the primary motor cortex, the supplementary meter area, and the premotor cortex. Exp. Brain Res.120, 114–128. 10.1007/s002210050384
46
TemizG.SébilleS. B.FrançoisC.BardinetE.KarachiC. (2020). The anatomo-functional organization of the hyperdirect cortical pathway to the subthalamic area using in vivo structural connectivity imaging in humans. Brain Struct. Funct.225, 551–565. 10.1007/s00429-019-02012-6
47
TokunoH.InaseM.NambuA.AkazawaT.MiyachiS.TakadaM. (1999). Corticostriatal projections from distal and proximal forelimb representations of the monkey primary motor cortex. Neurosci. Lett.269, 33–36. 10.1016/s0304-3940(99)00401-2
Summary
Keywords
non-human primate, anterograde tracing, motor cortex, basal ganglia, Parkinson
Citation
Borgognon S, Cottet J, Badoud S, Bloch J, Brunet J-F and Rouiller EM (2020) Cortical Projection From the Premotor or Primary Motor Cortex to the Subthalamic Nucleus in Intact and Parkinsonian Adult Macaque Monkeys: A Pilot Tracing Study. Front. Neural Circuits 14:528993. doi: 10.3389/fncir.2020.528993
Received
22 January 2020
Accepted
08 September 2020
Published
26 October 2020
Volume
14 - 2020
Edited by
Bin Song, McLean Hospital, United States
Reviewed by
Masahiko Takada, Kyoto University, Japan; Ken-ichi Amemori, Kyoto University, Japan
Updates
Copyright
© 2020 Borgognon, Cottet, Badoud, Bloch, Brunet and Rouiller.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Simon Borgognon simon.borgognon@unifr.ch; simon.borgognon@gmail.comorcid.org/0000-0002-4577-6553
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