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糖皮质激素对在化学成分明确的培养基中培养的人脂肪细胞前体细胞分化的促进作用。

Promoting effect of glucocorticoids on the differentiation of human adipocyte precursor cells cultured in a chemically defined medium.

作者信息

Hauner H, Entenmann G, Wabitsch M, Gaillard D, Ailhaud G, Negrel R, Pfeiffer E F

机构信息

Medizinische Klinik und Poliklinik, Universität Ulm, Federal Republic of Germany.

出版信息

J Clin Invest. 1989 Nov;84(5):1663-70. doi: 10.1172/JCI114345.

DOI:10.1172/JCI114345
PMID:2681273
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC304034/
Abstract

Stromal-vascular cells obtained from adult human subcutaneous adipose tissue were cultured in a chemically defined serum-free medium. In the presence of 0.2 nM triiodothyronine and 0.5 microM insulin, up to 25% of the cells were able to undergo terminal adipose differentiation within 18 d, as assessed by lipid accumulation and the expression of lipoprotein lipase (LPL) and glycerol-3-phosphate dehydrogenase (GPDH) activities. Addition of cortisol resulted in a potent dose-dependent stimulation of the adipose differentiation process. Cortisol could be replaced by dexamethasone and partly by aldosterone, but not by sex steroids. The proportion of differentiated cells was dependent upon the age of the donor; when isolated from young adults, up to 70% of the stromal-vascular cells expressed the adipocyte phenotype as compared with 5-10% when the cells were isolated from the oldest subjects. An inverse relationship was observed between the age of the 27 normal-weight donors and the extent of GPDH expression after maintenance of the cells for 18 d in chemically defined medium supplemented with insulin, triiodothyronine, and cortisol (r = -0.787, P less than 0.001). It is concluded that adult human adipose tissue still contains precursor cells that are able to undergo adipose differentiation in vitro. This improved culture system may offer the opportunity to characterize other adipogenic factors as well as antiadipogenic factors involved in the control of adipose tissue growth.

摘要

从成年人类皮下脂肪组织获取的基质血管细胞,在化学成分明确的无血清培养基中培养。在存在0.2 nM三碘甲状腺原氨酸和0.5 μM胰岛素的情况下,高达25%的细胞能够在18天内经历终末脂肪分化,这通过脂质积累以及脂蛋白脂肪酶(LPL)和甘油-3-磷酸脱氢酶(GPDH)活性的表达来评估。添加皮质醇会导致脂肪分化过程受到强大的剂量依赖性刺激。皮质醇可被地塞米松替代,部分可被醛固酮替代,但不能被性类固醇替代。分化细胞的比例取决于供体的年龄;从年轻成年人分离的基质血管细胞中,高达70%表达脂肪细胞表型,而从最年长者分离的细胞中这一比例为5 - 10%。在27名正常体重供体的年龄与在添加胰岛素、三碘甲状腺原氨酸和皮质醇的化学成分明确的培养基中培养18天后GPDH表达程度之间观察到负相关(r = -0.787,P < 0.001)。结论是成年人类脂肪组织仍含有能够在体外进行脂肪分化的前体细胞。这种改进的培养系统可能提供机会来表征参与脂肪组织生长控制的其他成脂因子以及抗成脂因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f4/304034/63771755a7d0/jcinvest00089-0303-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f4/304034/1175f1fe06d3/jcinvest00089-0303-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f4/304034/63771755a7d0/jcinvest00089-0303-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f4/304034/1175f1fe06d3/jcinvest00089-0303-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f4/304034/63771755a7d0/jcinvest00089-0303-b.jpg

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