Cellular and Nuclear Morphology…and Calcium Signaling: Revealing the Interplay between Structure and Function
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1
Goethe Center for Scientific Computing, Computational Neuroscience, Germany
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2
University of Heidelberg, Neurobiology, Germany
Calcium plays a pivotal role in relaying electrical signals of the cell to subcellular compartments, such as the nucleus. Since this one ion type is used by the cell for many processes a neuron needs to establish finely tuned calcium pathways in order to be able to differentiate multiple tasks, [1, 2, 3].
While it is known that neurons can actively change their shape upon neuronal activity, [4, 5, 6, 7], we here present novel findings of activity-regulated nuclear morphology, [8, 9]. With the help of an experimental and computational modeling approach, we show that hippocampal neurons can change the previously spherical shape of their nuclei to complex and infolded morphologies. This morphology regulation is demonstrated to be regulated by NMDA-receptor gated calcium, while synaptic and extra-synaptic NMDA-receptors elicit opposing effects on nuclear morphology, [8].
The structural alterations of the cell nucleus have significant effects on nuclear calcium dynamics. Compartmentalization of the nucleus, due to membrane infoldings, changes calcium frequencies, amplitudes and spatial distributions, [8, 10]. Since these parameters have been shown to control downstream events towards gene transcription, [11, 12], the results elucidate the cellular control of nuclear function with the help of morphology modulation. With respect to processes downstream of calcium, we show that histone H3 phosphorylation is closely linked to nuclear morphology. Investigating the nuclear morphologies of hippocampal neurons, two major classes were identified [9, 10]. One class contains non-infolded nuclei that have the function of calcium signal integrators, while the other class contains highly infolded nuclei, which function as frequency detectors of nuclear calcium, [10].
Extending this interdisciplinary approach of investigating structure/function relationships in neurons, the effects of cellular morphology – as well as the morphology of the endoplasmic reticulum and other organelles – on neuronal calcium signals is currently being investigated. This endeavor makes use of highly detailed, three-dimensional models of neuronal calcium dynamics, including the three-dimensional morphology of the cell and its organelles.
References
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[8] Wittmann M, Queisser G, Eder A, Wiegert JS, Bengtson CP, Hellwig A, Wittum G, Bading H: Synaptic activity induces dramatic changes in the geometry of the cell nucleus: interplay between nuclear structure, histone H3 phosphorylation and nuclear calcium signaling. J Neurosci 2009; 29:14687-700.
[9] Queisser G, Wittmann M, Bading H, Wittum G: Filtering, reconstruction and measurement of the geometry of nuclei from hippocampal neurons based on confocal microscopy data. J Biomed Opt 2008; 13:14009.
[10] Queisser G, Wiegert S, Bading H: Structural dynamics of the cell nucleus: Basis for morphology modulation of nuclear calcium signaling and gene transcription. Nucleus 2011, 2:2: 98-104.
[11] De Koninck P, Schulman H: Sensitivity of CaM kinase II to the frequency of Ca2+ oscillations. Science 1998, 279:227–230.
[12] Dolmetsch RE, Lewis RS, Goodnow CC, Healy JI: Differential activation of transcription factors induced by Ca2+ response amplitude and duration. Nature 1997, 386:855– 858.
Keywords:
Calcium Signaling,
cell morphology,
detailed modeling,
intracellular,
morphology modulation,
nucleus,
signaling,
three-dimensional
Conference:
Bernstein Conference 2012, Munich, Germany, 12 Sep - 14 Sep, 2012.
Presentation Type:
Poster
Topic:
Learning, plasticity, memory
Citation:
Breit
M,
Bengtson
C,
Hagenston
A,
Bading
H and
Queisser
G
(2012). Cellular and Nuclear Morphology…and Calcium Signaling: Revealing the Interplay between Structure and Function.
Front. Comput. Neurosci.
Conference Abstract:
Bernstein Conference 2012.
doi: 10.3389/conf.fncom.2012.55.00081
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Received:
23 May 2012;
Published Online:
12 Sep 2012.
*
Correspondence:
Prof. Gillian Queisser, Goethe Center for Scientific Computing, Computational Neuroscience, Frankfurt am Main, 60325, Germany, gillian.queisser@gcsc.uni-frankfurt.de