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.
References
[1]
Wajchenberg BL (2000) Subcutaneous and visceral adipose tissue: their relation to the metabolic syndrome. Endocr Rev 21: 697–738.
[2]
Pischon T, Boeing H, Hoffmann K, Bergmann M, Schulze MB et al (2008) General and abdominal adiposity and risk of death in Europe. N Engl J Med 359: 2105–20.
[3]
Pou KM, Massaro JM, Hoffmann U, Vasan RS, Maurovich-Horvat P et al (2007) Visceral and subcutaneous adipose tissue volumes are cross-sectionally related to markers of inflammation and oxidative stress: the Framingham Heart Study. Circulation 116: 1234–41.
[4]
Misra A, Garg A, Abate N, Peshock RM, Stray-Gundersen J et al (1997) Relationship of anterior and posterior subcutaneous abdominal fat to insulin sensitivity in nondiabetic men. Obes Res 5: 93–9.
[5]
Tran TT, Yamamoto Y, Gesta S, Kahn CR (2008) Beneficial effects of subcutaneous fat transplantation on metabolism. Cell Metab 7: 410–20.
[6]
Hocking SL, Chisholm DJ, James DE (2008) Studies of regional adipose transplantation reveal a unique and beneficial interaction between subcutaneous adipose tissue and the intra-abdominal compartment. Diabetologia 51: 900–2.
[7]
Baglioni S, Francalanci M, Squecco R, Lombardi A, Cantini G et al (2009) Characterization of human adult stem-cell populations isolated from visceral and subcutaneous adipose tissue. FASEB J 23: 3494–505.
[8]
Tchkonia T, Giorgadze N, Pirtskhalava T, Thomou T, DePonte M et al (2006) Fat depot-specific characteristics are retained in strains derived from single human preadipocytes. Diabetes 55: 2571–8.
[9]
Tchkonia T, Lenburg M, Thomou T, Giorgadze N, Frampton G et al (2007) Identification of depot-specific human fat cell progenitors through distinct expression profiles and developmental gene patterns. Am J Physiol Endocrinol Metab 292: E298–307.
[10]
Tchkonia T, Tchoukalova YD, Giorgadze N, Pirtskhalava T, Karagiannides I et al (2005) Abundance of two human preadipocyte subtypes with distinct capacities for replication, adipogenesis, and apoptosis varies among fat depots. Am J Physiol Endocrinol Metab 288: E267–77.
[11]
Lafontan M, Berlan M (2003) Do regional differences in adipocyte biology provide new pathophysiological insights? Trends Pharmacol Sci 24: 276–83.
[12]
Ramírez-Ponce MP, Mateos JC, Bellido JA (2003) Human Adipose Cells Have Voltage-dependent Potassium Currents. J Membrane Biol 196: 129–134.
[13]
Hu H, He ML, Tao R, Sun HY, Hu R et al (2009) Characterization of Ion Channels in Human Preadipocytes. J Cell Physiol 218: 427–435.
[14]
Ouadid-Ahidouch H, Roudbaraki M, Ahidouch M, Delcourt P, Prevarskaya N (2004) Cell-cycle-dependent expression of the large Ca2+-activated K+ channels in breast cancer cells. Biochem Biophys Res Commun 316: 244–251.
[15]
Sundelacruz S, Levin M, Kaplan DL (2008) Membrane potential controls adipogenic and osteogenic differentiation of mesenchymal stem cells. PLoS One 3: e3737.
[16]
Sundelacruz S, Levin M, Kaplan DL (2009) Role of membrane potential in the regulation of cell proliferation and differentiation. Stem Cell Rev 5: 231–46.
[17]
Blackiston DJ, McLaughlin KA, Levin M (2009) Bioelectric controls of cell proliferation: Ion channels, membrane voltage and the cell cycle. Cell Cycle 8: 3519–3528.
[18]
Heubach JF, Graf EM, Leutheuser J, Bock M, Balana B et al (2004) Electrophysiological properties of human mesenchymal stem cells. J Physiol 554: 659–72.
[19]
Benvenuti S, Saccardi R, Luciani P, Urbani S, Deledda C et al (2006) Neuronal differentiation of human mesenchymal stem cells: changes in the expression of the Alzheimer's disease-related gene seladin-1. Exp Cell Res. 312: 2592–604.
[20]
Nincheri P, Luciani P, Squecco R, Donati C, Bernacchioni C et al (2009) Sphingosine 1-phosphate induces differentiation of adipose tissue-derived mesenchymal stem cells towards smooth muscle cells. Cell Mol Life Sci 66: 1741–54.
[21]
Kern S, Eichler H, Stoeve J, Klüter H, Bieback K (2006) Comparative analysis of mesenchymal stem cells from bone marrow, umbilical cord blood, or adipose tissue. Stem Cells 24: 1294–301.
[22]
Lessard J, Sauvageau G (2003) Bmi-1 determines the proliferative capacity of normal and leukaemic stem cells. Nature 423: 255–60.
[23]
Park IK, Qian D, Kiel M, Becker MW, Pihalja M et al (2003) Bmi-1 is required for maintenance of adult self-renewing haematopoietic stem cells. Nature 423: 302–5.
[24]
Jacobs JJ, Kieboom K, Marino S, DePinho RA, van Lohuizen M (1999) The oncogene and Polycomb-group gene bmi-1 regulates cell proliferation and senescence through the ink4a locus. Nature 397: 164–8.
[25]
Virtue S, Vidal-Puig A (2008) It's not how fat you are, it's what you do with it that counts. PLoS Biol 6: e237.
[26]
Carey VJ, Walters EE, Colditz GA, Solomon CG, Willett WC et al (1997) Body fat distribution and risk of non-insulin-dependent diabetes mellitus in women. The Nurses' Health Study. Am J Epidemiol 145: 614–9.
[27]
Wang Z, Heshka S, Heymsfield SB, Shen W, Gallagher D (2005) A cellular-level approach to predicting resting energy expenditure across the adult years. Am J Clin Nutr 81: 799–806.
[28]
Tankó LB, Bagger YZ, Alexandersen P, Larsen PJ, Christiansen C (2003) Peripheral adiposity exhibits an independent dominant antiatherogenic effect in elderly women. Circulation 107: 1626–31.
[29]
Laviola L, Perrini S, Cignarelli A, Natalicchio A, Leonardini A et al (2006) Insulin signaling in human visceral and subcutaneous adipose tissue in vivo. Diabetes 55: 952–61.
[30]
Zierath JR, Livingston JN, Th?rne A, Bolinder J, Reynisdottir S et al (1998) 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. Diabetologia 41: 1343–54.
[31]
Perrini S, Laviola L, Cignarelli A, Melchiorre M, De Stefano F et al (2008) Fat depot-related differences in gene expression, adiponectin secretion, and insulin action and signalling in human adipocytes differentiated in vitro from precursor stromal cells. Diabetologia 51: 155–64.
[32]
Tchkonia T, Giorgadze N, Pirtskhalava T, Tchoukalova Y, Karagiannides I et al (2002) Fat depot origin affects adipogenesis in primary cultured and cloned human preadipocytes. Am J Physiol Regul Integr Comp Physiol 282: R1286–96.
[33]
Tchoukalova YD, Votruba SB, Tchkonia T, Giorgadze N, Kirkland JL et al (2010) Regional differences in cellular mechanisms of adipose tissue gain with overfeeding. Proc Natl Acad Sci U S A 107: 18226–31.
[34]
Kursawe R, Eszlinger M, Narayan D, Liu T, Bazuine M et al (2010) Cellularity and adipogenic profile of the abdominal subcutaneous adipose tissue from obese adolescents: association with insulin resistance and hepatic steatosis. Diabetes 59: 2288–96.
[35]
Cleveland-Donovan K, Maile LA, Tsiaras WG, Tchkonia T, Kirkland JL et al (2010) IGF-I activation of the AKT pathway is impaired in visceral but not subcutaneous preadipocytes from obese subjects. Endocrinology 151: 3752–63.
[36]
Fain JN, Madan AK, Hiler ML, Cheema P, Bahouth SW (2004) Comparison of the release of adipokines by adipose tissue, adipose tissue matrix, and adipocytes from visceral and subcutaneous abdominal adipose tissues of obese humans. Endocrinology 145: 2273–82.
[37]
Rodriguez AM, Elabd C, Delteil F, Astier J, Vernochet C et al (2004) Adipocyte differentiation of multipotent cells established from human adipose tissue. Biochem Biophys Res Commun 315: 255–63.
[38]
Rodriguez AM, Elabd C, Amri EZ, Ailhaud G, Dani C (2005) The human adipose tissue is a source of multipotent stem cells. Biochimie 87: 125–8.
[39]
Rodriguez AM, Pisani D, Dechesne CA, Turc-Carel C, Kurzenne JY et al (2005) Transplantation of a multipotent cell population from human adipose tissue induces dystrophin expression in the immunocompetent mdx mouse. J Exp Med 201: 1397–405.
[40]
Dicker A, Le Blanc K, Astr?m G, van Harmelen V, G?therstr?m C et al (2005) Functional studies of mesenchymal stem cells derived from adult human adipose tissue. Exp Cell Res 308: 283–90.
[41]
Guilak F, Lott KE, Awad HA, Cao Q, Hicok KC et al (2006) Clonal Analysis of the Differentiation Potential of Human Adipose-Derived Adult Stem Cells J. Cell. Physiol. 206: 229–237.
[42]
Fontaine C, Cousin W, Plaisant M, Dani C, Peraldi P (2008) Hedgehog signaling alters adipocyte maturation of human mesenchymal stem cells. Stem Cells 26: 1037–46.
[43]
Rubio D, Garcia-Castro J, Martín MC, de la Fuente R, Cigudosa JC et al (2005) Spontaneous human adult stem cell transformation. Cancer Res 65: 3035–9.
[44]
Vilalta M, Dégano IR, Bagó J, Gould D, Santos M et al (2008) 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. Stem Cells Dev 17: 993–1003.
[45]
Virtue S, Vidal-Puig A (2010) Adipose tissue expandability, lipotoxicity and the Metabolic Syndrome--an allostatic perspective. Biochim Biophys Acta 1801: 338-49. pp. 338–49.
[46]
Arner E, Westermark PO, Spalding KL, Britton T, Rydén M et al (2010) Adipocyte turnover: relevance to human adipose tissue morphology. Diabetes 59: 105–9.
[47]
Rigamonti A, Brennand K, Lau F, Cowan CA (2011) Rapid cellular turnover in adipose tissue. PLoS One 6: e17637.
[48]
Beltrami AP, Cesselli D, Bergamin N, Marcon P, Rigo S et al (2007) Multipotent cells can be generated in vitro from several adult human organs (heart, liver, and bone marrow). Blood 110: 3438–46.
[49]
Fasano CA, Phoenix TN, Kokovay E, Lowry N, Elkabetz Y et al (2009) Bmi-1 cooperates with Foxg1 to maintain neural stem cell self-renewal in the forebrain. Genes Dev 23: 561–74.
[50]
Song LB, Zeng MS, Liao WT, Zhang L, Mo HY et al (2006) Bmi-1 is a novel molecular marker of nasopharyngeal carcinoma progression and immortalizes primary human nasopharyngeal epithelial cells. Cancer Res 66: 6225–32.
[51]
Wang L, Jin Q, Lee JE, Su IH, Ge K (2010) Histone H3K27 methyltransferase Ezh2 represses Wnt genes to facilitate adipogenesis. Proc Natl Acad Sci U S A 107: 7317–22.
[52]
Abu-Remaileh M, Gerson A, Farago M, Nathan G, Alkalay I et al (2010) Oct-3/4 regulates stem cell identity and cell fate decisions by modulating Wnt/β-catenin signalling. EMBO J 29: 3236–48.
[53]
Mauriege P, Galitzky J, Berlan M, Lafontan M (1987) Heterogeneous distribution of beta and alpha-2 adrenoceptor binding sites in human fat cells from various fat deposits: functional consequences. Eur J Clin Invest 17: 156–65.
[54]
van Harmelen V, Dicker A, Rydén M, Hauner H, L?nnqvist F et al (2002) Increased lipolysis and decreased leptin production by human omental as compared with subcutaneous preadipocytes. Diabetes 51: 2029–36.
[55]
Nielsen S, Guo Z, Johnson CM, Hensrud DD, Jensen MD (2004) Splanchnic lipolysis in human obesity. J Clin Invest 113: 1582–8.
[56]
Bolinder J, Kager L, Ostman J, Arner P (1983) Differences at the receptor and postreceptor levels between human omental and subcutaneous adipose tissue in the action of insulin on lipolysis. Diabetes 32: 117–23.
[57]
Gavrilova O, Marcus-Samuels B, Graham D, Kim JK, Shulman GI et al (2000) Surgical implantation of adipose tissue reverses diabetes in lipoatrophic mice. J Clin Invest 105: 271–8.