Riera M F, Meroni S B, Schteingart H F, Pellizzari E H, Cigorraga S B
Centro de Investigaciones Endocrinológicas (CEDIE), Hospital de Niños 'Ricardo Gutiérrez', Gallo 1330, 1425 Buenos Aires, Argentina.
J Endocrinol. 2002 May;173(2):335-43. doi: 10.1677/joe.0.1730335.
By using cultured rat Sertoli cells as a model, both the action of basic fibroblast growth factor (bFGF) on lactate production and the site of this action were studied. bFGF stimulated Sertoli cell lactate production in a dose-dependent manner (basal: 7.3+/-0.5; 0.1 ng/ml bFGF: 7.5+/-0.5; 1 ng/ml bFGF: 7.5+/-0.6; 10 ng/ml bFGF: 10.3+/-1.0; 30 ng/ml bFGF: 15.2+/-1.5; 50 ng/ml bFGF: 15.4+/-1.6 microg/microg DNA). Two major sites for the action of this growth factor were identified. First, bFGF was shown to exert short- and long-term stimulatory effects on glucose transport (basal: 1170+/-102; 30 ng/ml bFGF for 120 min: 1718+/-152 and basal: 718+/-64; 30 ng/ml bFGF for 48 h: 1069+/-69 d.p.m./microg DNA respectively). Short-term bFGF stimulation of glucose transport was not inhibited by the protein synthesis inhibitor cycloheximide. These results indicate that short-term bFGF stimulation of glucose uptake does not involve an increase in the number of glucose transporters. On the other hand, stimulation with bFGF for periods of time longer than 12 h increased glucose transporter 1 (GLUT1) mRNA levels. These increased mRNA levels were probably ultimately responsible for the increments in glucose uptake that are observed in long-term treated cultures. Secondly, bFGF increased lactate dehydrogenase (LDH) activity (basal: 31.0+/-1.4; 30 ng/ml bFGF: 45.7+/- 2.4 mIU/microg DNA). The principal subunit component of those LDH isozymes that favors the transformation of pyruvate to lactate is subunit A. bFGF increased LDH A mRNA levels in a dose- and time-dependent manner. In summary, the results presented herein show that glucose transport, LDH activity and GLUT1 and LDH A mRNA levels are regulated by bFGF to achieve an increase in lactate production. These observed regulatory actions provide unequivocal evidence of the participation of bFGF in Sertoli cell lactate production which may be related to normal germ cell development.
以培养的大鼠支持细胞为模型,研究了碱性成纤维细胞生长因子(bFGF)对乳酸生成的作用及其作用位点。bFGF以剂量依赖的方式刺激支持细胞乳酸生成(基础值:7.3±0.5;0.1 ng/ml bFGF:7.5±0.5;1 ng/ml bFGF:7.5±0.6;10 ng/ml bFGF:10.3±1.0;30 ng/ml bFGF:15.2±1.5;50 ng/ml bFGF:15.4±1.6微克/微克DNA)。确定了该生长因子作用的两个主要位点。首先,bFGF对葡萄糖转运具有短期和长期刺激作用(基础值:1170±102;30 ng/ml bFGF处理120分钟:1718±152,基础值:718±64;30 ng/ml bFGF处理48小时:分别为1069±69 d.p.m./微克DNA)。蛋白质合成抑制剂环己酰亚胺不抑制bFGF对葡萄糖转运的短期刺激。这些结果表明,bFGF对葡萄糖摄取的短期刺激不涉及葡萄糖转运体数量的增加。另一方面,用bFGF刺激超过12小时会增加葡萄糖转运体1(GLUT1)mRNA水平。这些增加的mRNA水平可能最终导致长期处理培养物中观察到的葡萄糖摄取增加。其次,bFGF增加乳酸脱氢酶(LDH)活性(基础值:31.0±1.4;30 ng/ml bFGF:45.7±2.4 mIU/微克DNA)。那些有利于丙酮酸转化为乳酸的LDH同工酶的主要亚基成分是亚基A。bFGF以剂量和时间依赖的方式增加LDH A mRNA水平。总之,本文给出的结果表明,葡萄糖转运、LDH活性以及GLUT1和LDH A mRNA水平受bFGF调节,以实现乳酸生成增加。这些观察到的调节作用明确证明了bFGF参与支持细胞乳酸生成,这可能与正常生殖细胞发育有关。