Riera M F, Meroni S B, Gómez G E, Schteingart H F, Pellizzari E H, Cigorraga S B
Centro de Investigaciones Endocrinológicas (CEDIE), Hospital de Niños "R Gutiérrez,", Gallo 1330, Buenos Aires, 1425, Argentina.
Gen Comp Endocrinol. 2001 Apr;122(1):88-97. doi: 10.1006/gcen.2001.7619.
One of the "nurse cell" functions of Sertoli cells is to provide lactate for the energy production in spermatocytes and spermatids. The present study shows that, as in porcine Sertoli cells, interleukin (IL)1beta and follicle-stimulating hormone (FSH) increase lactate production in rat Sertoli cells (basal, 9.1 +/- 1.0; FSH (100 ng/ml), 16.6 +/- 2.0; IL1beta (50 ng/ml), 13.3 +/- 1.6 microg/microg DNA). Increments in glucose uptake (basal, 1083 +/- 70; FSH, 2686 +/- 128; IL1beta, 1899 +/- 74 dpm/microg DNA), lactic dehydrogenase (LDH) activity (basal, 36.6 +/- 4.1; FSH, 52.2 +/- 4.9; IL1beta, 55.3 +/- 5.1 mUI/microg DNA), LDH A mRNA levels, and redistribution of LDH isozymes are involved in these stimulatory effects. Differences in the period required by IL1beta to increase glucose uptake, as compared with the porcine model, have been observed. In addition, tumor necrosis factor alpha (TNFalpha), one of the major stimulators for lactate production in porcine Sertoli cells, does not control the secretion of this glucose metabolite in rat Sertoli cells. Lactate production may be regulated differently among mammals.
支持细胞的“滋养细胞”功能之一是为精母细胞和精子细胞的能量产生提供乳酸。本研究表明,与猪支持细胞一样,白细胞介素(IL)1β和促卵泡激素(FSH)可增加大鼠支持细胞的乳酸产生(基础值为9.1±1.0;FSH(100 ng/ml)时为16.6±2.0;IL1β(50 ng/ml)时为13.3±1.6μg/μg DNA)。葡萄糖摄取增加(基础值为1083±70;FSH时为2686±128;IL1β时为1899±74 dpm/μg DNA)、乳酸脱氢酶(LDH)活性增加(基础值为36.6±4.1;FSH时为52.2±4.9;IL1β时为55.3±5.1 mUI/μg DNA)、LDH A mRNA水平以及LDH同工酶的重新分布都参与了这些刺激作用。与猪模型相比,观察到IL1β增加葡萄糖摄取所需时间存在差异。此外,肿瘤坏死因子α(TNFα)是猪支持细胞中乳酸产生的主要刺激因子之一,但它并不控制大鼠支持细胞中这种葡萄糖代谢产物的分泌。不同哺乳动物之间乳酸产生的调节方式可能有所不同。