Greg Brown Diabetes and Endocrinology Laboratory, Sydney Medical School, University of Sydney, Sydney, NSW, Australia.
New South Wales Health Pathology, Australia.
Biosci Rep. 2020 May 29;40(5). doi: 10.1042/BSR20194262.
Transforming growth factor β (TGFβ) a multifunctional cytokine is known to regulate cell proliferation, differentiation, migration and survival. Although there is variable expression of modulators of TGFβ action during differentiation, a differential effect on fat cell metabolism at the different stages of adipocyte differentiation was unclear. In the present study, 3T3L1 cells were used as an in vitro model to study the effect of TGFβ on adipogenic and thermogenic markers at various stages of preadipocyte to mature adipocyte differentiation. As in our earlier studies on the effect of TGFβ on CEBP's, we used a standard differentiation mix, and one with the addition of rosiglitazone. RhTGFβ1 was added to undifferentiated adipocytes (preadipocytes) and to adipocytes at day 0 (commitment stage) as well as day 10 (terminal differentiation). Cellular responses in terms of Pref1, PPARγ, TLE3, PGC1α, PRDM16, UCP1 and UCP2 mRNA levels and selected protein products, were determined. Increases in PPARγ, PRDM16, UCP1 and UCP2 mRNA and decreases in Pref1 are good indicators of successful differentiation. The early addition of rhTGFβ1 during commitment stage decreased PPARγ, PRDM16, TLE3, UCP1 and UCP2 mRNA and decreased PRDM16 protein consistent with our earlier report on the inhibition of CEBP's by TGFβ and CCN2. The addition of rhTGFβ1 to mature adipocyte at day 10 increased UCP1 mRNA and increased PRDM16 and UCP1 proteins. In the present study, our results suggest that TGFβ1 added late enhances the thermogenic potential of mature cells and causes 3T3L1 cells to differentiate to resemble brown or beige rather than white adipose tissue.
转化生长因子 β(TGFβ)是一种多功能细胞因子,已知其可调节细胞增殖、分化、迁移和存活。尽管在分化过程中,TGFβ 作用的调节剂的表达存在差异,但在脂肪细胞分化的不同阶段,其对脂肪细胞代谢的影响尚不清楚。在本研究中,我们使用 3T3L1 细胞作为体外模型,研究 TGFβ 在脂肪细胞前体细胞向成熟脂肪细胞分化的不同阶段对脂肪形成和生热标记物的影响。在我们之前关于 TGFβ 对 CEBP 的影响的研究中,我们使用了标准分化混合物和添加罗格列酮的混合物。rhTGFβ1 被添加到未分化的脂肪细胞(前脂肪细胞)和分化的第 0 天(承诺阶段)和第 10 天(终末分化)的脂肪细胞中。根据 Pref1、PPARγ、TLE3、PGC1α、PRDM16、UCP1 和 UCP2 mRNA 水平和选定的蛋白质产物来确定细胞反应。PPARγ、PRDM16、UCP1 和 UCP2 mRNA 的增加以及 Pref1 的减少是分化成功的良好指标。在承诺阶段早期添加 rhTGFβ1 会降低 PPARγ、PRDM16、TLE3、UCP1 和 UCP2 mRNA 的表达,并降低 PRDM16 蛋白的表达,这与我们之前关于 TGFβ 和 CCN2 抑制 CEBP 的报告一致。在第 10 天将 rhTGFβ1 添加到成熟脂肪细胞中会增加 UCP1 mRNA 的表达,并增加 PRDM16 和 UCP1 蛋白的表达。在本研究中,我们的结果表明,晚期添加的 TGFβ1 增强了成熟细胞的生热潜力,并使 3T3L1 细胞分化为类似于棕色或米色脂肪组织,而不是白色脂肪组织。