Mini Review ARTICLE
Adipose Tissue Inflammation Induces B Cell Inflammation and Decreases B Cell Function in Aging
- Department of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, United States
Aging is the greatest risk factor for developing chronic diseases. Inflamm-aging, the age-related increase in low-grade chronic inflammation, may be a common link in age-related diseases. This review summarizes recent published data on potential cellular and molecular mechanisms of the age-related increase in inflammation, and how these contribute to decreased humoral immune responses in aged mice and humans. Briefly, we cover how aging and related inflammation decrease antibody responses in mice and humans, and how obesity contributes to the mechanisms for aging through increased inflammation. We also report data in the literature showing adipose tissue infiltration with immune cells and how these cells are recruited and contribute to local and systemic inflammation. We show that several types of immune cells infiltrate the adipose tissue and these include macrophages, neutrophils, NK cells, innate lymphoid cells, eosinophils, T cells, B1, and B2 cells. Our main focus is how the adipose tissue affects immune responses, in particular B cell responses and antibody production. The role of leptin in generating inflammation and decreased B cell responses is also discussed. We report data published by us and by other groups showing that the adipose tissue generates pro-inflammatory B cell subsets which induce pro-inflammatory T cells, promote insulin resistance, and secrete pathogenic autoimmune antibodies.
Aging and Related Inflammation Decrease Antibody Responses in Mice and Humans
Aged mice and humans have a poor immune response against infectious agents and vaccines (1). The antibody-mediated humoral immune response is qualitatively deficient with the production of antibodies of lower affinity (2–5) and with self-reactivity (6–8). Defects in T cells (9–11), B cells (12, 13), and antigen-presenting cells (14, 15) have been reported and all contribute to the age-related decrease in antibody production.
Our laboratory has characterized age-related autonomous B cell defects, which are responsible for sub-optimal antibody responses of elderly individuals to infections and vaccines (16–20). These include a reduction in activation-induced cytidine deaminase (AID), the enzyme necessary for class switch recombination, somatic hypermutation, and IgG production, as well as in E47 (13, 21), a key transcription factor regulating AID (22). Because AID correlates with optimal B cell function, it can be used as a predictive marker of optimal B cell response in humans (16, 17). The decrease in AID (4) leads to a reduced ability to generate higher affinity antibodies, e.g., to the influenza vaccine.
Aging is characterized by “inflamm-aging” (23), a low-grade chronic inflammation, which is a risk factor for morbidity and mortality of elderly individuals as it is implicated in the pathogenesis of several disabling diseases of the elderly such as type-2 diabetes mellitus (24), osteoporosis (25), Alzheimer’s disease (26), rheumatoid arthritis (27), and coronary heart disease (28). Our results have shown B cell functional deficiencies with increased inflammation with age in both mice (29) and humans (19). In particular, we demonstrated that increased TNF-α either in serum or in B cells contributes to sub-optimal antibody responses and we consider this to be a condition where the B cells have been made “refractory” to further stimulation by chronic stimulation with inflammatory cytokines.
Obesity as a Mechanism of Aging
Among risk factors associated with disability and frailty, obesity seems to be a major contributor. Obesity is an inflammatory condition in which the innate immune system is chronically activated. Obesity contributes to pathologic conditions such as type-2 diabetes mellitus (30–32), cancer (33), psoriasis (34), atherosclerosis (35), and inflammatory bowel disease (36). Obesity is associated with sub-optimal immune responses in mice (37, 38) and humans (39).
The adipose tissue is generally separated into visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) (40). The SAT accounts for ~80% of human adipose tissue, but the VAT is more metabolically active (41), and VAT accumulation is a greater predictor of obesity-associated mortality.
Fat mass increases with age in mice (42–44) and humans (45) and this is associated with low-grade chronic inflammation which contributes to the development of insulin resistance (IR) which also increases with age. Aging induces a significant increase in fat mass, redistribution of body fat with increased VAT, and decreased SAT, as well as ectopic VAT deposition. All these are strongly associated with worse health conditions in healthy elderly individuals (46). Moreover, aging may significantly affect AT function by changing the profile of inflammatory mediators produced by the adipocytes, modifying pre-adipocyte number and function and AT infiltration of macrophages (46), and other lymphocytes (see below).
It has recently been proposed that increased cellular stress in the adipocytes with age induces cellular senescence, which in turn leads to impaired removal of lipotoxic fatty acids, and increased secretion of pro-inflammatory cytokines and chemokines, due to the activation of the innate, and adaptive immune systems (47). These pro-inflammatory processes not only amplify each other but also have systemic consequences. These results suggest that cellular senescence is a stress-induced adaptive response that develops through major metabolic and secretory readjustments. This can occur at any time during life.
Studies in humans have shown that individuals with higher total and abdominal adiposity have shorter telomeres (48), suggesting that obesity may accelerate the aging process. Telomere length is inversely associated with body mass index (BMI), waist to hip ratio, independently of sex, age, fasting glucose and insulin, lipid and lipoprotein concentrations, physical activity, smoking status, and other metabolic risk factors.
Adipose Tissue Inflammation
The AT is a major immunologically active organ that contributes to systemic inflammation through the secretion of pro-inflammatory cytokines and chemokines, as well as adipokines (49). Immune cells represent two-thirds of the stromal vascular fraction, and therefore the expansion of the AT during high-fat diet increases its ability to act as an immunological organ able to control systemic inflammation and metabolism. Chronic inflammation and immune cell infiltration in the AT are hallmark of obesity-associated IR and glucose intolerance.
Increased inflammation in the AT is the result of increased intrinsic inflammation in the adipocytes, which operates in a positive feedback loop, whereby the accumulation of infiltrating immune cells secrete pro-inflammatory cytokines and chemokines following interaction with the adipocytes. This feedback loop explains not only local but also systemic inflammation via the circulating immune cells. Infiltrating immune cells are drawn to the AT and become more inflammatory and these cells would generate sub-optimal immune responses in obesity by circulating to the peripheral lymphoid organs.
Immune cells infiltrating the AT include macrophages, neutrophils, NK cells, innate lymphoid cells (ILCs), eosinophils, T cells, B1, and B2 cells. The cellular composition of AT is dynamic and is regulated by acute and chronic stimuli including diet, body weight, fasting. In general, neutrophils are the first cells that infiltrate the expanding AT during high-fat diet, followed by macrophages, B, T, and NK cells (43).
In response to energy increase, adipocytes undergo hypertrophy, hyperplasia, and die, releasing in the extracellular space their cytoplasmic content including the lipid droplets, which cause the release of danger-associated molecular patterns such as free fatty acids, excess glucose, ATP, ceramides, cholesterol. All these activate macrophages expressing TLRs and NLRs, activate the inflammasome and initiate the AT inflammatory response, leading to the recruitment of monocytes, and increased polarization of macrophages to an inflammatory M1-like phenotype. Macrophages represent the primary source of TNF-α in the AT (50).
Neutrophils promote IR through the release of elastase (51), myeloperoxidase, and extracellular traps (ETs) (52). Aberrant production and reduced clearance of ETs can lead to accumulation of immunogenic self-antigens and promotion of autoimmune diseases (53).
NK cells significantly increase in number in the AT of mice fed with a high-fat diet. NK cells regulate the number and the function of AT macrophages through production of pro-inflammatory cytokines, mainly TNF-α, and thereby contribute to the development of IR. Depletion of NK cells using neutralizing antibodies has been shown to protect from IR (54).
Innate lymphoid cells have also been shown to promote IR, in particular ILC1s, which trigger M1 macrophage activation and inhibit ILC2 function through IFN-γ, thereby contributing to chronic inflammation and possibly perpetuating obesity-associated IR (55, 56).
In obese individuals, pro-inflammatory Th1 cells infiltrate the AT (57) and activate M1 macrophages (58), whereas in lean individuals Th2 cells, T regulatory, and iNKT cells are predominant in the VAT and promote secretion of IL-10 and other anti-inflammatory cytokines from M2 macrophages which maintain insulin sensitivity. The abdominal SAT has been reported to be dangerous as well in promoting inflammation (59).
Studies elucidating B cell function in obesity are limited, although B cells have recently emerged as crucial players in regulating inflammation in murine AT, by presenting antigens to T cells, secreting pro-inflammatory cytokines, and pathogenic antibodies (43). In mice, B2 cells accumulate in the AT before T cells, shortly after the initiation of a high-fat diet (60). We have recently shown that the adipocytes in murine VAT make several pro-inflammatory chemokines (CXCL10/CCL2/CCL5), which may recruit B2 cells as they express the corresponding receptors (CXCR3/CCR2/CCR3) (61). We believe that B2 cells infiltrating the VAT become more inflammatory and these cells would generate sub-optimal immune responses once they circulate back to the peripheral lymphoid tissues (Figure 1). B2 cells may also be recruited to the AT through leukotriene LTB4/LTB4R1 signaling (62).
Figure 1. Mechanisms by which the visceral adipose tissue (VAT) impairs antibody responses. The adipocytes in the VAT secrete more pro-inflammatory chemokines which attract B cells via chemokine receptors, as well as pro-inflammatory cytokines. Age-associated B cells (ABCs) are preferentially induced and we hypothesize that these cells make pro-inflammatory cytokines and pathogenic antibodies. Marginal zone B cells are not affected. Immune cells traffic to the spleen and periphery where there are more ABC in aged and obese mice. Before antigen stimulation the cells secrete increased amounts of inflammatory cytokines (TNF-α/IL-6), making them refractory to further stimulation. Fewer antibody-secreting cells producing less Ig are made after antigen stimulation of “refractory” B cells.
B1 cells can also be found in the AT, although at lower percentages when compared with B2 cells, with B1a (but not B1b) being increased in the AT mice fed high-fat diet (43). These cells secrete IgM antibodies which have no effect on metabolic parameters in contrast with IgG, but they clear self-antigens and therefore have a regulatory role by limiting B2 cell activation and by promoting B cell tolerance. B10 producing B1 cells in the AT have been shown to have protective effects against diet-induced obesity and IR (63).
The early recruitment of B cells promotes T cell activation and pro-inflammatory cytokine production (43). B cells are activated in the expanding AT by pro-inflammatory stimuli and release cytokines or chemokines, thus contributing to local and systemic inflammation (64, 65). Antibodies secreted by B cells can also regulate lipid absorption from the gut and Bnull mice show reduction in lipid absorption (66). This role of B cells in lipid adsorption could also shape mucosal immunity and change the gut microbiota (43, 67). Moreover, murine (44) and human B cells (39) support T cell inflammation.
The ongoing apoptosis in the AT, due to increases in fat mass, and consequent hypoxia, induces the release of “self” antigens, including cell-free DNA, and the release of class switched IgG antibodies which form immune complexes with “self” antigens, which in turn activate complement (C1q/C1qR/C3/C3a) and Fc receptors on immune cells, leading to enhanced local inflammation, remodeling of the AT, impairment of adipocyte function and of nutrient metabolism, and exacerbation of obesity-associated conditions. This represents a novel mechanism by which DNA released from cells dying in the AT may attract immune cells expressing TLRs, which may propagate the inflammatory response, as recently shown in mouse macrophages (68).
Obesity is also associated with altered composition of the gut microbiota, increased intestinal permeability, and translocation of gut bacterial products into the blood. These include lipopolysaccharide and unmethylated CpG DNA, which may exert effects systemically or locally in the AT (69, 70). Aberrant production and recognition of nucleic acid antigens has been suggested to promote activation of immune cells in metabolic tissues, leading to the secretion of pro-inflammatory cytokines (71).
How the Adipose Tissue Affects Antibody Responses?
Obesity is associated with increased susceptibility to bacterial, viral, and fungal infections (72, 73) and obese individuals develop more post-surgical infections than lean individuals (74, 75). Moreover, overweight children have impaired antibody responses to tetanus toxin (76). Similarly, high-fat diet has been shown to increase mortality in mice infected with influenza (37). Contributing mechanisms seem to be defects in the generation and maintenance of memory CD8+ T cells (77), as well as impaired lung wound healing (78). The response to the influenza vaccine (39, 79) and to the Hepatitis B vaccine (80) are also compromised in individuals with obesity.
B cell function has been shown to be affected by leptin, the adipocyte-derived cytokine, member of the IL-6 superfamily, linking nutritional status with neuroendocrine, and immune functions, whose plasma levels correlate with the amount of body fat and BMI. The role of leptin in inflammation is supported by the studies in ob/ob mice which are leptin-deficient and have reduced secretion of Th1 cytokines (IL-2/IFN-γ/TNF-α/IL-18), and increased production of Th2 cytokines (IL-4/IL-10) (81–84). Leptin suppresses appetite in mice and humans (85, 86). High-serum levels of leptin contribute to the inflammatory state of the adipose tissue associated with obesity (87, 88). In individuals with obesity, leptin levels are associated with leptin resistance (86). Leptin activates human peripheral blood B cells from both young and elderly individuals to secrete pro-inflammatory cytokines (IL-6/TNF-α) and this occurs through activation of JAK2/STAT3 and p38MAPK/ERK1/2 signaling pathways (89, 90). In our recently published article, we stimulated B cells from lean individuals in vitro with leptin. We found pro-inflammatory signaling pathways upregulated (phospho-STAT3, crucial for TNF-α production) and anti-inflammatory pathways down-regulated (phospho-AMPK, crucial for antibody production), similar to what we observed in B cells from individuals with obesity (39).
We have recently discovered further mechanisms through which AT inflammation contributes to decreased B cell responses in old mice (61). We found AID in stimulated splenic B cells negatively correlated with epididymal fat size, showing for the first time a role of AT in the down-regulation of B cell function in aged mice. When we measured the percentages of the major peripheral B cell subsets [follicular (FO), age-associated B cells (ABCs), and marginal zone] in the spleens and epididymal VAT of young and old mice, we found reduced percentages of the FO subset in the spleen of old versus young mice and concomitant increased percentages of the pro-inflammatory ABC subset as previously shown (29, 91–93). Importantly, percentages of FO were reduced (and percentages of ABC were increased) even more in VAT versus spleen.
We have recently shown that the VAT promotes the differentiation of FO into ABCs (61). We demonstrated this by co-culturing in transwells for 72 h adipocytes and splenic B cells, in the absence of any additional mitogenic stimulus. Results showed increased percentages of ABC, which was similar to what we have observed in the VAT. To clarify if this was the result of increased expansion and survival of ABC versus FO B cells, death of FO B cells, loss of cell markers, or a combination of these, we sorted splenic FO and ABC from old mice and measured by qPCR the expression of several markers described to be differentially expressed in these two subsets by a transcriptome analysis performed previously by the Marrack group (92). We selected five markers among those most differentially expressed in FO versus ABC: Prdm1 (Blimp-1), FcεRγ1, Tbx21 (T-bet), Kifc3, Stx3. All these markers were found expressed at higher levels in ABC versus FO, as expected. Then, we cultured sorted splenic FO B cells from old mice in the presence of adipocyte-conditioned medium (ACM) and we found that the ACM induced significant increased expression of ABC markers when compared with complete medium, suggesting that FO B cells differentiated into ABC. In order to evaluate if the ACM contains factors which may be responsible for FO differentiation into ABC, as suggested by an article recently published by Cancro’s group (94), we measured by qPCR production of IL-21/IFN-γ by the adipocytes. Results showed that adipocytes express mRNA for both cytokines.
B cells have been shown to promote IR through activation of T cells and production of pro-inflammatory, pathogenic, autoimmune antibodies (43). We also found production of class switched IgG2c antibodies by B cells in the VAT, and these antibodies were detected by intracellular staining of VAT ABCs in the absence of stimulation, suggesting that ABC in the VAT are already highly pre-activated, and are refractory to further stimulation (61). IgG2c have been noted to be more autoimmune (95). Our results have shown for the first time that IgG2c antibodies are made in the VAT by ABCs, and the expression of MHC class I and class II on B cells has been reported to be crucial (43), suggesting that B cell-mediated antigen presentation to T cells is required for their pathogenic effects.
It has been shown that B cell depletion with an anti-CD20 antibody ameliorates metabolic disease, and transfer of IgG from high-fat diet mice rapidly induces IR (43). T cells can also be necessary for a pathogenic effect, as adoptive transfer of CD4+ T cells into high-fat diet RAGnull mice, lacking both B and T cells, was able to block weight gain and reverse IR for months, predominately through anti-inflammatory Th2 cells (96).
In conclusion, we have summarized emerging data on potential cellular and molecular mechanisms for the age-related increase in inflammation and how these lead to functional decline and decreased humoral responses in aged mice and humans. Overall, it appears that persistent inflammation is the driver of age-related diseases and that down regulation of inflammatory pathways may help to reduce onset and severity of age-related chronic diseases. Key challenges for the field will be to identify therapeutic strategies of intervention to lose weight will reduce body fat, systemic inflammation, and the pathogenic role of immune cells. Importantly, immune responses to fight infections will also be improved.
All authors were involved in writing the article and had final approval of the submitted and published versions.
Conflict of Interest Statement
The research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This study was supported by NIH AG023717 (BB), AG32576 (DF/BB), AI096446, and AG042826 (BB/DF).
1. Boraschi D, Del Giudice G, Dutel C, Ivanoff B, Rappuoli R, Grubeck-Loebenstein B. Ageing and immunity: addressing immune senescence to ensure healthy ageing. Vaccine (2010) 28(21):3627–31. doi:10.1016/j.vaccine.2010.03.035
2. van Dijk-Hard I, Soderstrom I, Feld S, Holmberg D, Lundkvist I. Age-related impaired affinity maturation and differential D-JH gene usage in human VH6-expressing B lymphocytes from healthy individuals. Eur J Immunol (1997) 27(6):1381–6. doi:10.1002/eji.1830270613
3. Gibson KL, Wu YC, Barnett Y, Duggan O, Vaughan R, Kondeatis E, et al. B-cell diversity decreases in old age and is correlated with poor health status. Aging Cell (2009) 8(1):18–25. doi:10.1111/j.1474-9726.2008.00443.x
4. Khurana S, Frasca D, Blomberg B, Golding H. AID activity in B cells strongly correlates with polyclonal antibody affinity maturation in-vivo following pandemic 2009-H1N1 vaccination in humans. PLoS Pathog (2012) 8(9):e1002920. doi:10.1371/journal.ppat.1002920
5. Goenka R, Scholz JL, Naradikian MS, Cancro MP. Memory B cells form in aged mice despite impaired affinity maturation and germinal center kinetics. Exp Gerontol (2014) 54:109–15. doi:10.1016/j.exger.2013.12.013
7. Duggal NA, Upton J, Phillips AC, Sapey E, Lord JM. An age-related numerical and functional deficit in CD19(+) CD24(hi) CD38(hi) B cells is associated with an increase in systemic autoimmunity. Aging Cell (2013) 12(5):873–81. doi:10.1111/acel.12114
10. Haynes L, Eaton SM, Burns EM, Randall TD, Swain SL. CD4 T cell memory derived from young naive cells functions well into old age, but memory generated from aged naive cells functions poorly. Proc Natl Acad Sci U S A (2003) 100(25):15053–8. doi:10.1073/pnas.2433717100
12. Frasca D, Van der Put E, Riley RL, Blomberg BB. Reduced Ig class switch in aged mice correlates with decreased E47 and activation-induced cytidine deaminase. J Immunol (2004) 172(4):2155–62. doi:10.4049/jimmunol.172.4.2155
13. Frasca D, Landin AM, Lechner SC, Ryan JG, Schwartz R, Riley RL, et al. Aging down-regulates the transcription factor E2A, activation-induced cytidine deaminase, and Ig class switch in human B cells. J Immunol (2008) 180(8):5283–90. doi:10.4049/jimmunol.180.8.5283
15. Panda A, Qian F, Mohanty S, van Duin D, Newman FK, Zhang L, et al. Age-associated decrease in TLR function in primary human dendritic cells predicts influenza vaccine response. J Immunol (2010) 184(5):2518–27. doi:10.4049/jimmunol.0901022
16. Frasca D, Diaz A, Romero M, Landin AM, Phillips M, Lechner SC, et al. Intrinsic defects in B cell response to seasonal influenza vaccination in elderly humans. Vaccine (2010) 28(51):8077–84. doi:10.1016/j.vaccine.2010.10.023
17. Frasca D, Diaz A, Romero M, Phillips M, Mendez NV, Landin AM, et al. Unique biomarkers for B-cell function predict the serum response to pandemic H1N1 influenza vaccine. Int Immunol (2012) 24(3):175–82. doi:10.1093/intimm/dxr123
18. Frasca D, Diaz A, Romero M, Mendez NV, Landin AM, Blomberg BB. Effects of age on H1N1-specific serum IgG1 and IgG3 levels evaluated during the 2011-2012 influenza vaccine season. Immun Ageing (2013) 10(1):14. doi:10.1186/1742-4933-10-14
19. Frasca D, Diaz A, Romero M, Landin AM, Blomberg BB. High TNF-alpha levels in resting B cells negatively correlate with their response. Exp Gerontol (2014) 54:116–22. doi:10.1016/j.exger.2014.01.004
20. Frasca D, Diaz A, Romero M, Landin AM, Blomberg BB. Cytomegalovirus (CMV) seropositivity decreases B cell responses to the influenza vaccine. Vaccine (2015) 33(12):1433–9. doi:10.1016/j.vaccine.2015.01.071
21. Frasca D, Diaz A, Romero M, Ferracci F, Blomberg BB. MicroRNAs miR-155 and miR-16 decrease AID and E47 in B cells from elderly individuals. J Immunol (2015) 195(5):2134–40. doi:10.4049/jimmunol.1500520
23. Franceschi C, Valensin S, Bonafe M, Paolisso G, Yashin AI, Monti D, et al. The network and the remodeling theories of aging: historical background and new perspectives. Exp Gerontol (2000) 35(6–7):879–96. doi:10.1016/S0531-5565(00)00172-8
24. Lindholm E, Bakhtadze E, Cilio C, Agardh E, Groop L, Agardh CD. Association between LTA, TNF and AGER polymorphisms and late diabetic complications. PLoS One (2008) 3(6):e2546. doi:10.1371/journal.pone.0002546
26. Holmes C, Cunningham C, Zotova E, Woolford J, Dean C, Kerr S, et al. Systemic inflammation and disease progression in Alzheimer disease. Neurology (2009) 73(10):768–74. doi:10.1212/WNL.0b013e3181b6bb95
27. Isaacs JD. Therapeutic agents for patients with rheumatoid arthritis and an inadequate response to tumour necrosis factor-alpha antagonists. Expert Opin Biol Ther (2009) 9(12):1463–75. doi:10.1517/14712590903379494
29. Frasca D, Romero M, Diaz A, Alter-Wolf S, Ratliff M, Landin AM, et al. A molecular mechanism for TNF-alpha-mediated downregulation of B cell responses. J Immunol (2012) 188(1):279–86. doi:10.4049/jimmunol.1003964
33. Renehan AG, Tyson M, Egger M, Heller RF, Zwahlen M. Body-mass index and incidence of cancer: a systematic review and meta-analysis of prospective observational studies. Lancet (2008) 371(9612):569–78. doi:10.1016/S0140-6736(08)60269-X
34. Setty AR, Curhan G, Choi HK. Obesity, waist circumference, weight change, and the risk of psoriasis in women: Nurses’ Health Study II. Arch Intern Med (2007) 167(15):1670–5. doi:10.1001/archinte.167.15.1670
35. Casas R, Sacanella E, Estruch R. The immune protective effect of the mediterranean diet against chronic low-grade inflammatory diseases. Endocr Metab Immune Disord Drug Targets (2014) 14(4):245–54. doi:10.2174/1871530314666140922153350
36. Hass DJ, Brensinger CM, Lewis JD, Lichtenstein GR. The impact of increased body mass index on the clinical course of Crohn’s disease. Clin Gastroenterol Hepatol (2006) 4(4):482–8. doi:10.1016/j.cgh.2005.12.015
38. Milner JJ, Sheridan PA, Karlsson EA, Schultz-Cherry S, Shi Q, Beck MA. Diet-induced obese mice exhibit altered heterologous immunity during a secondary 2009 pandemic H1N1 infection. J Immunol (2013) 191(5):2474–85. doi:10.4049/jimmunol.1202429
39. Frasca D, Ferracci F, Diaz A, Romero M, Lechner S, Blomberg BB. Obesity decreases B cell responses in young and elderly individuals. Obesity (Silver Spring) (2016) 24(3):615–25. doi:10.1002/oby.21383
41. Yang YK, Chen M, Clements RH, Abrams GA, Aprahamian CJ, Harmon CM. Human mesenteric adipose tissue plays unique role versus subcutaneous and omental fat in obesity related diabetes. Cell Physiol Biochem (2008) 22(5–6):531–8. doi:10.1159/000185527
42. Wu D, Ren Z, Pae M, Guo W, Cui X, Merrill AH, et al. Aging up-regulates expression of inflammatory mediators in mouse adipose tissue. J Immunol (2007) 179(7):4829–39. doi:10.4049/jimmunol.179.7.4829
43. Winer DA, Winer S, Shen L, Wadia PP, Yantha J, Paltser G, et al. B cells promote insulin resistance through modulation of T cells and production of pathogenic IgG antibodies. Nat Med (2011) 17(5):610–7. doi:10.1038/nm.2353
44. DeFuria J, Belkina AC, Jagannathan-Bogdan M, Snyder-Cappione J, Carr JD, Nersesova YR, et al. B cells promote inflammation in obesity and type 2 diabetes through regulation of T-cell function and an inflammatory cytokine profile. Proc Natl Acad Sci U S A (2013) 110(13):5133–8. doi:10.1073/pnas.1215840110
45. van Harmelen V, Skurk T, Rohrig K, Lee YM, Halbleib M, Aprath-Husmann I, et al. Effect of BMI and age on adipose tissue cellularity and differentiation capacity in women. Int J Obes Relat Metab Disord (2003) 27(8):889–95. doi:10.1038/sj.ijo.0802314
47. Tchkonia T, Morbeck DE, Von Zglinicki T, Van Deursen J, Lustgarten J, Scrable H, et al. Fat tissue, aging, and cellular senescence. Aging Cell (2010) 9(5):667–84. doi:10.1111/j.1474-9726.2010.00608.x
50. Weisberg SP, McCann D, Desai M, Rosenbaum M, Leibel RL, Ferrante AW Jr. Obesity is associated with macrophage accumulation in adipose tissue. J Clin Invest (2003) 112(12):1796–808. doi:10.1172/JCI19246
51. Talukdar S, Oh DY, Bandyopadhyay G, Li D, Xu J, McNelis J, et al. Neutrophils mediate insulin resistance in mice fed a high-fat diet through secreted elastase. Nat Med (2012) 18(9):1407–12. doi:10.1038/nm.2885
53. Hakkim A, Furnrohr BG, Amann K, Laube B, Abed UA, Brinkmann V, et al. Impairment of neutrophil extracellular trap degradation is associated with lupus nephritis. Proc Natl Acad Sci U S A (2010) 107(21):9813–8. doi:10.1073/pnas.0909927107
54. Lee BC, Kim MS, Pae M, Yamamoto Y, Eberle D, Shimada T, et al. Adipose natural killer cells regulate adipose tissue macrophages to promote insulin resistance in obesity. Cell Metab (2016) 23(4):685–98. doi:10.1016/j.cmet.2016.03.002
55. Yang D, Yang W, Tian Z, van Velkinburgh JC, Song J, Wu Y, et al. Innate lymphoid cells as novel regulators of obesity and its-associated metabolic dysfunction. Obes Rev (2016) 17(6):485–98. doi:10.1111/obr.12397
56. Boulenouar S, Michelet X, Duquette D, Alvarez D, Hogan AE, Dold C, et al. Adipose type one innate lymphoid cells regulate macrophage homeostasis through targeted cytotoxicity. Immunity (2017) 46(2):273–86. doi:10.1016/j.immuni.2017.01.008
57. Nishimura S, Manabe I, Nagasaki M, Eto K, Yamashita H, Ohsugi M, et al. CD8+ effector T cells contribute to macrophage recruitment and adipose tissue inflammation in obesity. Nat Med (2009) 15(8):914–20. doi:10.1038/nm.1964
59. McLaughlin T, Deng A, Yee G, Lamendola C, Reaven G, Tsao PS, et al. Inflammation in subcutaneous adipose tissue: relationship to adipose cell size. Diabetologia (2010) 53(2):369–77. doi:10.1007/s00125-009-1496-3
60. Duffaut C, Galitzky J, Lafontan M, Bouloumie A. Unexpected trafficking of immune cells within the adipose tissue during the onset of obesity. Biochem Biophys Res Commun (2009) 384(4):482–5. doi:10.1016/j.bbrc.2009.05.002
61. Frasca D, Diaz A, Romero M, Vazquez T, Blomberg BB. Obesity induces pro-inflammatory B cells and impairs B cell function in old mice. Mech Ageing Dev (2017) 162:91–9. doi:10.1016/j.mad.2017.01.004
62. Ying W, Wollam J, Ofrecio JM, Bandyopadhyay G, El Ouarrat D, Lee YS, et al. Adipose tissue B2 cells promote insulin resistance through leukotriene LTB4/LTB4R1 signaling. J Clin Invest (2017) 127(3):1019–30. doi:10.1172/JCI90350
63. Wu L, Parekh VV, Hsiao J, Kitamura D, Van Kaer L. Spleen supports a pool of innate-like B cells in white adipose tissue that protects against obesity-associated insulin resistance. Proc Natl Acad Sci U S A (2014) 111(43):E4638–47. doi:10.1073/pnas.1324052111
66. Shulzhenko N, Morgun A, Hsiao W, Battle M, Yao M, Gavrilova O, et al. Crosstalk between B lymphocytes, microbiota and the intestinal epithelium governs immunity versus metabolism in the gut. Nat Med (2011) 17(12):1585–93. doi:10.1038/nm.2505
67. Winer DA, Winer S, Chng MH, Shen L, Engleman EG. B Lymphocytes in obesity-related adipose tissue inflammation and insulin resistance. Cell Mol Life Sci (2014) 71(6):1033–43. doi:10.1007/s00018-013-1486-y
68. Nishimoto S, Fukuda D, Higashikuni Y, Tanaka K, Hirata Y, Murata C, et al. Obesity-induced DNA released from adipocytes stimulates chronic adipose tissue inflammation and insulin resistance. Sci Adv (2016) 2(3):e1501332. doi:10.1126/sciadv.1501332
69. Henao-Mejia J, Elinav E, Jin C, Hao L, Mehal WZ, Strowig T, et al. Inflammasome-mediated dysbiosis regulates progression of NAFLD and obesity. Nature (2012) 482(7384):179–85. doi:10.1038/nature10809
71. Revelo XS, Ghazarian M, Chng MH, Luck H, Kim JH, Zeng K, et al. Nucleic acid-targeting pathways promote inflammation in obesity-related insulin resistance. Cell Rep (2016) 16(3):717–30. doi:10.1016/j.celrep.2016.06.024
73. O’Shea D, Corrigan M, Dunne MR, Jackson R, Woods C, Gaoatswe G, et al. Changes in human dendritic cell number and function in severe obesity may contribute to increased susceptibility to viral infection. Int J Obes (Lond) (2013) 37(11):1510–3. doi:10.1038/ijo.2013.16
78. O’Brien KB, Vogel P, Duan S, Govorkova EA, Webby RJ, McCullers JA, et al. Impaired wound healing predisposes obese mice to severe influenza virus infection. J Infect Dis (2012) 205(2):252–61. doi:10.1093/infdis/jir729
79. Ovsyannikova IG, White SJ, Larrabee BR, Grill DE, Jacobson RM, Poland GA. Leptin and leptin-related gene polymorphisms, obesity, and influenza A/H1N1 vaccine-induced immune responses in older individuals. Vaccine (2014) 32(7):881–7. doi:10.1016/j.vaccine.2013.12.009
83. Martin-Romero C, Santos-Alvarez J, Goberna R, Sanchez-Margalet V. Human leptin enhances activation and proliferation of human circulating T lymphocytes. Cell Immunol (2000) 199(1):15–24. doi:10.1006/cimm.1999.1594
85. Halaas JL, Gajiwala KS, Maffei M, Cohen SL, Chait BT, Rabinowitz D, et al. Weight-reducing effects of the plasma protein encoded by the obese gene. Science (1995) 269(5223):543–6. doi:10.1126/science.7624777
88. John BJ, Irukulla S, Abulafi AM, Kumar D, Mendall MA. Systematic review: adipose tissue, obesity and gastrointestinal diseases. Aliment Pharmacol Ther (2006) 23(11):1511–23. doi:10.1111/j.1365-2036.2006.02915.x
89. Agrawal S, Gollapudi S, Su H, Gupta S. Leptin activates human B cells to secrete TNF-alpha, IL-6, and IL-10 via JAK2/STAT3 and p38MAPK/ERK1/2 signaling pathway. J Clin Immunol (2011) 31(3):472–8. doi:10.1007/s10875-010-9507-1
91. Hao Y, O’Neill P, Naradikian MS, Scholz JL, Cancro MP. A B-cell subset uniquely responsive to innate stimuli accumulates in aged mice. Blood (2011) 118(5):1294–304. doi:10.1182/blood-2011-01-330530
92. Rubtsov AV, Rubtsova K, Fischer A, Meehan RT, Gillis JZ, Kappler JW, et al. Toll-like receptor 7 (TLR7)-driven accumulation of a novel CD11c(+) B-cell population is important for the development of autoimmunity. Blood (2011) 118(5):1305–15. doi:10.1182/blood-2011-01-331462
93. Ratliff M, Alter S, Frasca D, Blomberg BB, Riley RL. In senescence, age-associated B cells secrete TNFalpha and inhibit survival of B-cell precursors. Aging Cell (2013) 12(2):303–11. doi:10.1111/acel.12055
94. Naradikian MS, Myles A, Beiting DP, Roberts KJ, Dawson L, Herati RS, et al. Cutting edge: IL-4, IL-21, and IFN-gamma interact to govern T-bet and CD11c expression in TLR-activated B cells. J Immunol (2016) 197(4):1023–8. doi:10.4049/jimmunol.1600522
Keywords: aging, obesity, inflammation, immunity, antibody responses
Citation: Frasca D and Blomberg BB (2017) Adipose Tissue Inflammation Induces B Cell Inflammation and Decreases B Cell Function in Aging. Front. Immunol. 8:1003. doi: 10.3389/fimmu.2017.01003
Received: 18 April 2017; Accepted: 04 August 2017;
Published: 28 August 2017
Edited by:Graham Pawelec, University of Tübingen, Germany
Reviewed by:Shahram Salek-ardakani, Pfizer, United States
David Dombrowicz, Institut national de la santé et de la recherche médicale, France
Copyright: © 2017 Frasca and Blomberg. 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) or licensor 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: Bonnie B. Blomberg, firstname.lastname@example.org