Functional Differences in Visceral and Subcutaneous Fat Pads Originate from Differences in the Adipose Stem Cell

Metabolic pathologies mainly originate from adipose tissue (AT) dysfunctions. AT differences are associated with fat-depot anatomic distribution in subcutaneous (SAT) and visceral omental (VAT) pads. We address the question whether the functional differences between the two compartments may be present early in the adipose stem cell (ASC) instead of being restricted to the mature adipocytes. Using a specific human ASC model, we evaluated proliferation/differentiation of ASC from abdominal SAT-(S-ASC) and VAT-(V-ASC) paired biopsies in parallel as well as the electrophysiological properties and functional activity of ASC and their in vitro-derived adipocytes. A dramatic difference in proliferation and adipogenic potential was observed between the two ASC populations, S-ASC having a growth rate and adipogenic potential significantly higher than V-ASC and giving rise to more functional and better organized adipocytes. To our knowledge, this is the first comprehensive electrophysiological analysis of ASC and derived-adipocytes, showing electrophysiological properties, such as membrane potential, capacitance and K+-current parameters which confirm the better functionality of S-ASC and their derived adipocytes. We document the greater ability of S-ASC-derived adipocytes to secrete adiponectin and their reduced susceptibility to lipolysis. These features may account for the metabolic differences observed between the SAT and VAT. Our findings suggest that VAT and SAT functional differences originate at the level of the adult ASC which maintains a memory of its fat pad of origin. Such stem cell differences may account for differential adipose depot susceptibility to the development of metabolic dysfunction and may represent a suitable target for specific therapeutic approaches.

[1]  S. Bernard,et al.  Adipocyte Turnover: Relevance to Human Adipose Tissue Morphology , 2009, Diabetes.

[2]  F. Lönnqvist,et al.  Increased lipolysis and decreased leptin production by human omental as compared with subcutaneous preadipocytes. , 2002, Diabetes.

[3]  A. Madan,et al.  Comparison of the release of adipokines by adipose tissue, adipose tissue matrix, and adipocytes from visceral and subcutaneous abdominal adipose tissues of obese humans. , 2004, Endocrinology.

[4]  R. DePinho,et al.  The oncogene and Polycomb-group gene bmi-1 regulates cell proliferation and senescence through the ink4a locus , 1999, Nature.

[5]  P. Arner,et al.  Differences at the Receptor and Postreceptor Levels Between Human Omental and Subcutaneous Adipose Tissue in the Action of Insulin on Lipolysis , 1983, Diabetes.

[6]  G. Perigli,et al.  Characterization of human adult stem‐cell populations isolated from visceral and subcutaneous adipose tissue , 2009, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[7]  F. Speizer,et al.  The Nurses' Health Study , 1978, The American journal of nursing.

[8]  F. Guilak,et al.  Clonal analysis of the differentiation potential of human adipose‐derived adult stem cells , 2006, Journal of cellular physiology.

[9]  D. James,et al.  Studies of regional adipose transplantation reveal a unique and beneficial interaction between subcutaneous adipose tissue and the intra-abdominal compartment , 2008, Diabetologia.

[10]  Samuel W. Cushman,et al.  Cellularity and Adipogenic Profile of the Abdominal Subcutaneous Adipose Tissue From Obese Adolescents: Association With Insulin Resistance and Hepatic Steatosis , 2010, Diabetes.

[11]  Min Zhu,et al.  Human adipose tissue is a source of multipotent stem cells. , 2002, Molecular biology of the cell.

[12]  M. Roudbaraki,et al.  Cell-cycle-dependent expression of the large Ca2+-activated K+ channels in breast cancer cells. , 2004, Biochemical and biophysical research communications.

[13]  N. Gerry,et al.  Identification of depot-specific human fat cell progenitors through distinct expression profiles and developmental gene patterns. , 2007, American journal of physiology. Endocrinology and metabolism.

[14]  R. Giorgino,et al.  Insulin signaling in human visceral and subcutaneous adipose tissue in vivo. , 2006, Diabetes.

[15]  S. Heymsfield,et al.  A cellular-level approach to predicting resting energy expenditure across the adult years. , 2005, American Journal of Clinical Nutrition.

[16]  R M Peshock,et al.  Relationship of anterior and posterior subcutaneous abdominal fat to insulin sensitivity in nondiabetic men. , 1997, Obesity research.

[17]  Irving L. Weissman,et al.  Bmi-1 is required for maintenance of adult self-renewing haematopoietic stem cells , 2003, Nature.

[18]  C. Dani,et al.  Hedgehog Signaling Alters Adipocyte Maturation of Human Mesenchymal Stem Cells , 2008, Stem cells.

[19]  A. Vidal-Puig,et al.  Adipose tissue expandability, lipotoxicity and the Metabolic Syndrome--an allostatic perspective. , 2010, Biochimica et biophysica acta.

[20]  Yuji Yamamoto,et al.  Beneficial effects of subcutaneous fat transplantation on metabolism. , 2008, Cell metabolism.

[21]  A. Vidal-Puig,et al.  It's Not How Fat You Are, It's What You Do with It That Counts , 2008, PLoS biology.

[22]  Michael Levin,et al.  Bioelectric controls of cell proliferation: Ion channels, membrane voltage and the cell cycle , 2009, Cell cycle.

[23]  Claus Christiansen,et al.  Peripheral Adiposity Exhibits an Independent Dominant Antiatherogenic Effect in Elderly Women , 2003, Circulation.

[24]  Peter Arner,et al.  Regional difference in insulin inhibition of non-esterified fatty acid release from human adipocytes: relation to insulin receptor phosphorylation and intracellular signalling through the insulin receptor substrate-1 pathway , 1998, Diabetologia.

[25]  M. Jensen,et al.  Regional differences in cellular mechanisms of adipose tissue gain with overfeeding , 2010, Proceedings of the National Academy of Sciences.

[26]  J. Murabito,et al.  Visceral and Subcutaneous Adipose Tissue Volumes Are Cross-Sectionally Related to Markers of Inflammation and Oxidative Stress: The Framingham Heart Study , 2007, Circulation.

[27]  R. A. Forse,et al.  Fat Depot–Specific Characteristics Are Retained in Strains Derived From Single Human Preadipocytes , 2006, Diabetes.

[28]  F. Francini,et al.  Sphingosine 1-phosphate induces differentiation of adipose tissue-derived mesenchymal stem cells towards smooth muscle cells , 2009, Cellular and Molecular Life Sciences.

[29]  F. Francini,et al.  Neuronal differentiation of human mesenchymal stem cells: changes in the expression of the Alzheimer's disease-related gene seladin-1. , 2006, Experimental cell research.

[30]  M. Jensen,et al.  Abundance of two human preadipocyte subtypes with distinct capacities for replication, adipogenesis, and apoptosis varies among fat depots. , 2005, American journal of physiology. Endocrinology and metabolism.

[31]  B. Wajchenberg Subcutaneous and visceral adipose tissue: their relation to the metabolic syndrome. , 2000, Endocrine reviews.

[32]  M. Jensen,et al.  Fat depot origin affects adipogenesis in primary cultured and cloned human preadipocytes. , 2002, American journal of physiology. Regulatory, integrative and comparative physiology.

[33]  Hermann Eichler,et al.  Comparative Analysis of Mesenchymal Stem Cells from Bone Marrow, Umbilical Cord Blood, or Adipose Tissue , 2006, Stem cells.

[34]  A. Fainsod,et al.  Oct‐3/4 regulates stem cell identity and cell fate decisions by modulating Wnt/β‐catenin signalling , 2010, The EMBO journal.

[35]  G. Sauvageau,et al.  Bmi-1 determines the proliferative capacity of normal and leukaemic stem cells , 2003, Nature.

[36]  R. Giorgino,et al.  Fat depot-related differences in gene expression, adiponectin secretion, and insulin action and signalling in human adipocytes differentiated in vitro from precursor stromal cells , 2007, Diabetologia.

[37]  L. Maile,et al.  IGF-I activation of the AKT pathway is impaired in visceral but not subcutaneous preadipocytes from obese subjects. , 2010, Endocrinology.

[38]  Yun-Fei Xia,et al.  Bmi-1 is a novel molecular marker of nasopharyngeal carcinoma progression and immortalizes primary human nasopharyngeal epithelial cells. , 2006, Cancer research.

[39]  P. Arner,et al.  Functional studies of mesenchymal stem cells derived from adult human adipose tissue. , 2005, Experimental cell research.

[40]  G A Colditz,et al.  Body fat distribution and risk of non-insulin-dependent diabetes mellitus in women. The Nurses' Health Study. , 1997, American journal of epidemiology.

[41]  C. Dani,et al.  Adipocyte differentiation of multipotent cells established from human adipose tissue. , 2004, Biochemical and biophysical research communications.

[42]  C. Lau,et al.  Characterization of ion channels in human preadipocytes , 2009, Journal of cellular physiology.

[43]  John T. Dimos,et al.  Bmi-1 cooperates with Foxg1 to maintain neural stem cell self-renewal in the forebrain. , 2009, Genes & development.

[44]  C. Schneider,et al.  Multipotent cells can be generated in vitro from several adult human organs (heart, liver, and bone marrow). , 2007, Blood.

[45]  M. Schulze,et al.  General and abdominal adiposity and risk of death in Europe. , 2008, The New England journal of medicine.

[46]  J. Cigudosa,et al.  Spontaneous human adult stem cell transformation. , 2005, Cancer research.

[47]  Donald D Hensrud,et al.  Splanchnic lipolysis in human obesity. , 2004, The Journal of clinical investigation.

[48]  S. Bernard,et al.  Adipocyte Turnover: Relevance to Human Adipose Tissue , 2010 .

[49]  M. Berlan,et al.  Do regional differences in adipocyte biology provide new pathophysiological insights? , 2003, Trends in pharmacological sciences.

[50]  C. Dani,et al.  Transplantation of a multipotent cell population from human adipose tissue induces dystrophin expression in the immunocompetent mdx mouse , 2005, The Journal of experimental medicine.

[51]  J. C. Mateos,et al.  Human Adipose Cells Have Voltage-dependent Potassium Currents , 2003, The Journal of Membrane Biology.

[52]  David L. Kaplan,et al.  Role of Membrane Potential in the Regulation of Cell Proliferation and Differentiation , 2009, Stem Cell Reviews and Reports.

[53]  U. Ravens,et al.  Electrophysiological properties of human mesenchymal stem cells , 2004, The Journal of physiology.

[54]  D. García-Olmo,et al.  Biodistribution, long-term survival, and safety of human adipose tissue-derived mesenchymal stem cells transplanted in nude mice by high sensitivity non-invasive bioluminescence imaging. , 2008, Stem cells and development.

[55]  David L. Kaplan,et al.  Membrane Potential Controls Adipogenic and Osteogenic Differentiation of Mesenchymal Stem Cells , 2008, PloS one.

[56]  M. Berlan,et al.  Heterogeneous distribution of beta and alpha‐2 adrenoceptor binding sites in human fat cells from various fat deposits: functional consequences , 1987, European journal of clinical investigation.

[57]  Ji-Eun Lee,et al.  Histone H3K27 methyltransferase Ezh2 represses Wnt genes to facilitate adipogenesis , 2010, Proceedings of the National Academy of Sciences.

[58]  Chad A. Cowan,et al.  Rapid Cellular Turnover in Adipose Tissue , 2011, PloS one.

[59]  G. Shulman,et al.  Surgical implantation of adipose tissue reverses diabetes in lipoatrophic mice. , 2000, The Journal of clinical investigation.