Anderson L A, McTernan P G, Barnett A H, Kumar S
Division of Medical Sciences, Department of Medicine, Queen Elizabeth Hospital, University of Birmingham, Birmingham, United Kingdom B15 2TH.
J Clin Endocrinol Metab. 2001 Oct;86(10):5045-51. doi: 10.1210/jcem.86.10.7955.
The gender-specific differences in body fat distribution suggest that sex steroids play an important role in regulating body fat distribution. Sex steroids may regulate adipose tissue mass by altering adipocyte number and size. The effects of various sex steroids on in vitro proliferation of preadipocytes from both sc and omental fat depots was investigated in men and women. Abdominal sc and omental preadipocytes from men (n = 14) and women (8 premenopausal and 7 postmenopausal) were cultured in the presence of 17beta-E2 (10(-7)-10(-9) M), estrone (10(-7)-10(-9) M), or dehydrotestosterone (DHT) (10(-7)-10(-9) M), and the rate of proliferation was measured over time (1-96 h) by DNA accumulation assays (micromoles per microg) and [(3)H]thymidine incorporation (disintegrations per min). In sc preadipocytes the rate of proliferation was increased between 24-48 h with E2 (10(-7) M) in both men (P = 0.028) and women (P = 0.017). Subcutaneous preadipocytes from women were more responsive to E2 in stimulating proliferation than those from men (women vs. men, DNA assay, 24 h, P = 0.014). In omental preadipocytes the increase in the rate of proliferation occurred at 24 h with E2 (10(-7) M) in women (P = 0.034) and at 48 h in men (P = 0.031). Gender appeared to influence the rate of proliferation by E2 in omental preadipocytes, with maximal stimulation of proliferation at 48 h in preadipocytes from women treated with E2 (10(-7) M; p = 0.007) compared with 72 h in preadipocyte cells from men (P = 0.048), as shown by DNA assay. Both estrone and the androgen DHT had no significant gender- or site-specific effect on the rate of proliferation at any time point. All DNA content data were further validated by thymidine incorporation analysis. In summary, E2 stimulates the rate of proliferation of preadipocytes in a dose-dependent manner, with significant gender- and site-specific differences. Neither estrone nor DHT affected adipocyte mass through proliferation of preadipocytes in this study. In conclusion, E2 may act as an important local factor influencing the proliferation of preadipocytes that may affect fat cell number in a depot- and gender-specific pattern in human abdominal sc and omental adipose tissue.
体脂分布的性别差异表明,性类固醇在调节体脂分布中起重要作用。性类固醇可能通过改变脂肪细胞数量和大小来调节脂肪组织量。研究了各种性类固醇对男性和女性皮下及网膜脂肪组织前脂肪细胞体外增殖的影响。将男性(n = 14)以及女性(8名绝经前和7名绝经后)的腹部皮下和网膜前脂肪细胞在17β-雌二醇(10⁻⁷ - 10⁻⁹ M)、雌酮(10⁻⁷ - 10⁻⁹ M)或脱氢睾酮(DHT)(10⁻⁷ - 10⁻⁹ M)存在的情况下进行培养,并通过DNA积累测定法(每微克微摩尔数)和[³H]胸腺嘧啶核苷掺入法(每分钟衰变数)随时间(1 - 96小时)测量增殖率。在皮下前脂肪细胞中,E2(10⁻⁷ M)在24 - 48小时之间使男性(P = 0.028)和女性(P = 0.017)的增殖率均增加。女性的皮下前脂肪细胞在刺激增殖方面比男性的更易对E2产生反应(女性与男性相比,DNA测定,24小时,P = 0.014)。在网膜前脂肪细胞中,E2(10⁻⁷ M)使女性的增殖率在24小时时增加(P = 0.034),男性在48小时时增加(P = 0.031)。性别似乎影响E2对网膜前脂肪细胞增殖率的作用,用E2(10⁻⁷ M)处理的女性前脂肪细胞在48小时时增殖刺激最大(P = 0.007),而男性前脂肪细胞在72小时时增殖刺激最大(P = 0.048),DNA测定显示如此。在任何时间点,雌酮和雄激素DHT对增殖率均无显著的性别或部位特异性影响。所有DNA含量数据均通过胸腺嘧啶核苷掺入分析进一步验证。总之,E2以剂量依赖性方式刺激前脂肪细胞的增殖率,存在显著的性别和部位特异性差异。在本研究中,雌酮和DHT均未通过前脂肪细胞增殖影响脂肪细胞量。总之,E2可能作为一种重要的局部因子影响前脂肪细胞的增殖,这可能以部位和性别特异性模式影响人类腹部皮下和网膜脂肪组织中的脂肪细胞数量。