Reyne Y, Nouguès J, Dulor J P
Unité Différenciation Cellulaire et Croissance, INRA-ENSA, Montpellier, France.
In Vitro Cell Dev Biol. 1989 Aug;25(8):747-52. doi: 10.1007/BF02623728.
A serum-free, hormone-supplemented medium containing insulin, transferrin, and triiodothyronine (ITT medium), able to support differentiation of rat adipose precursor cells, has been used to study the regulation of the development of adipocytes in the rabbit. Adipose conversion was assessed by the appearance of glycerol-3-phosphate dehydrogenase activity. Stromal-vascular cells from rabbit perirenal adipose tissue differentiated to a very low extent or not at all in ITT medium. Supplementation of ITT medium with growth hormone or fibroblast growth factor did not increase the proportion of differentiated cells. In contrast, rabbit stromal-vascular cells were able to differentiate in ITT medium supplemented with glucocorticoids (dexamethasone, corticosterone) whereas sex steroids (beta-estradiol, testosterone, progesterone) did not affect the differentiation process. In the presence of both dexamethasone and insulin, 20 to 50% of rabbit stromal-vascular cells differentiated into adipocytes within 2 wk of culture. The stimulatory actions of dexamethasone or insulin were dose-dependent. Insulin-like growth Factor-I (IGF-I), did not replace insulin under our culture conditions and had only a slight effect when added along with dexamethasone (100 nM) and insulin (1.7 nM). The results suggest that glucocorticoids, in association with insulin, may play an important role in the development of adipocytes from rabbit precursor cells.
一种不含血清、添加了胰岛素、转铁蛋白和三碘甲状腺原氨酸的培养基(ITT培养基),能够支持大鼠脂肪前体细胞的分化,已被用于研究兔脂肪细胞发育的调控。通过3-磷酸甘油脱氢酶活性的出现来评估脂肪转化。来自兔肾周脂肪组织的基质血管细胞在ITT培养基中分化程度极低或根本不分化。在ITT培养基中添加生长激素或成纤维细胞生长因子并不会增加分化细胞的比例。相反,兔基质血管细胞能够在添加了糖皮质激素(地塞米松、皮质酮)的ITT培养基中分化,而性类固醇(β-雌二醇、睾酮、孕酮)并不影响分化过程。在同时存在地塞米松和胰岛素的情况下,20%至50%的兔基质血管细胞在培养2周内分化为脂肪细胞。地塞米松或胰岛素的刺激作用具有剂量依赖性。在我们的培养条件下,胰岛素样生长因子-I(IGF-I)不能替代胰岛素,并且在与地塞米松(100 nM)和胰岛素(1.7 nM)一起添加时只有轻微作用。结果表明,糖皮质激素与胰岛素一起,可能在兔前体细胞向脂肪细胞的发育中起重要作用。