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Identification of specific cell-surface markers of adipose-derived stem cells from subcutaneous and visceral fat depots.

ABSTRACT: Adipose-derived stem/stromal cells (ASCs) from the anatomically distinct subcutaneous and visceral depots of white adipose tissue (WAT) differ in their inherent properties. However, little is known about the molecular identity and definitive markers of ASCs from these depots. In this study, ASCs from subcutaneous fat (SC-ASCs) and visceral fat (VS-ASCs) of omental region were isolated and studied. High-content image screening of over 240 cell-surface markers identified several potential depot-specific markers of ASCs. Subsequent studies revealed consistent predominant expression of CD10 in SC-ASCs and CD200 in VS-ASCs across 12 human subjects and in mice. CD10-high-expressing cells sorted from SC-ASCs differentiated better than their CD10-low-expressing counterparts, whereas CD200-low VS-ASCs differentiated better than CD200-high VS-ASCs. The expression of CD10 and CD200 is thus depot-dependent and associates with adipogenic capacities. These markers will offer a valuable tool for tracking and screening of depot-specific stem cell populations.

SUBMITTER: Ong WK

PROVIDER: S-EPMC3923222 | biostudies-literature | 2014 Feb

REPOSITORIES: biostudies-literature

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Identification of specific cell-surface markers of adipose-derived stem cells from subcutaneous and visceral fat depots.

Ong Wee Kiat WK Tan Chuen Seng CS Chan Kai Li KL Goesantoso Grace Gandi GG Chan Xin Hui Derryn XH Chan Edmund E Yin Jocelyn J Yeo Chia Rou CR Khoo Chin Meng CM So Jimmy Bok Yan JB Shabbir Asim A Toh Sue-Anne SA Han Weiping W Sugii Shigeki S

Stem cell reports 20140206 2

Adipose-derived stem/stromal cells (ASCs) from the anatomically distinct subcutaneous and visceral depots of white adipose tissue (WAT) differ in their inherent properties. However, little is known about the molecular identity and definitive markers of ASCs from these depots. In this study, ASCs from subcutaneous fat (SC-ASCs) and visceral fat (VS-ASCs) of omental region were isolated and studied. High-content image screening of over 240 cell-surface markers identified several potential depot-sp ...[more]

PMID: 24527391

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Project description:OBJECTIVE:Persons living with HIV (PLWH) well treated on antiretroviral therapies remain at risk for ensuing arterial disease. We investigated the relationship between adipose depots and biomarkers of arterial injury and inflammation to gain insight into the link between body composition and CVD risk. DESIGNS/METHODS:One hundred and fifty-five HIV-infected and 70 non-HIV infected individuals were well phenotyped for body composition. Adipose depots were assessed via single-slice abdominal computed tomography (CT). Circulating markers of arterial disease and generalized inflammation [lipoprotein-associated phospholipase A2 (LpPLA2), oxidized low-density lipoprotein (oxLDL), high-sensitivity cardiac troponin T (hs-cTnT), high-sensitivity C-reactive protein (hsCRP)] were evaluated. RESULTS:Despite similar BMI and visceral adipose tissue (VAT), HIV-infected individuals had significantly lower subcutaneous adipose tissue [SAT, 199 (126-288) vs. 239 (148-358) cm(2), P?=?0.04] than non-HIV infected individuals. Among HIV-infected individuals, reduced SAT inversely correlated with LpPLA2 (??=?-0.19, P?=?0.02) and hs-cTnT (??=?-0.24, P?=?0.004), whereas increased VAT significantly and positively related to LpPLA2 (??=?0.25, P?=?0.003), oxLDL (??=?0.28, P?=?0.0005), hs-cTnT (??=?0.28, P?=?0.0007) and hsCRP (??=?0.32, P?=??<?0.0001). Similar analyses among the non-HIV infected individuals revealed significant relationships between SAT and LpPLA2 (??=?-0.24, P?=?0.05), as well as VAT and LpPLA2 (??=?0.37, P?=?0.002), oxLDL (??=?0.24, P?=?0.05) and hsCRP (??=?0.29, P?=?.02). In modelling performed among the HIV group, simultaneously controlling for VAT, SAT, age and relevant HIV-related parameters, reduced SAT was an independent predictor of LpPLA2 (P?=?0.04) and hs-cTnT (P?=?0.005) and increased VAT was an independent predictor of LpPLA2 (P?=?0.001), oxLDL (P?=?0.02), hs-cTnT (P?=?0.04) and hsCRP (P?=?0.04). CONCLUSION:Fat redistribution phenotypes, characterized by SAT loss and/or VAT accumulation, may be linked to arterial injury and inflammation in HIV.

Dataset Information

Identification of specific cell-surface markers of adipose-derived stem cells from subcutaneous and visceral fat depots.

Publications

Identification of specific cell-surface markers of adipose-derived stem cells from subcutaneous and visceral fat depots.

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