Nagaike M, Hirao S, Tajima H, Noji S, Taniguchi S, Matsumoto K, Nakamura T
Department of Biology, Faculty of Science, Kyushu University, Fukuoka, Japan.
J Biol Chem. 1991 Dec 5;266(34):22781-4.
Hepatocyte growth factor (HGF), a most potent growth factor for mature hepatocytes may act as a trigger for liver regeneration. We reported that HGF strongly stimulates DNA synthesis of rabbit renal tubular cells in secondary culture (Igawa, T., Kanda, S., Kanetake, H., Saitoh, Y., Ichihara, A., Tomita, Y., and Nakamura, T. (1991) Biochem. Biophys. Res. Commun. 174, 831-838). To investigate whether or not HGF is involved in renal regeneration, we examined changes in HGF mRNA, HGF activity, and HGF receptor in the rat kidney following unilateral nephrectomy or treatment with carbon tetrachloride (CCl4). In the intact kidney, the HGF mRNA increased markedly reaching a maximum 6 h after unilateral nephrectomy, followed by an increase of HGF activity at 12 h after the surgery. The marked increase in HGF mRNA and HGF activity was also found in the kidney of rats treated with CCl4. Results of in situ hybridization suggested that cells producing HGF in the kidney are endothelial cells. The number of HGF receptors on renal plasma membranes decreased to 30% of the normal value 12 h after unilateral nephrectomy, with no change in the Kd value. The HGF receptor was greatly diminished 24 h after the operation, and recovery to 60% of the normal level was evident 1 week after the operation. Because the decrease in HGF binding may result from internalization of the HGF receptor, the HGF may bind to its receptor in vivo and act as a mitogen for renal epithelial cells. HGF may function as a renotropic factor during renal regeneration after kidney injury.
肝细胞生长因子(HGF)是一种对成熟肝细胞作用最强的生长因子,可能是肝脏再生的触发因素。我们曾报道,HGF能强烈刺激传代培养的兔肾小管细胞的DNA合成(Igawa, T., Kanda, S., Kanetake, H., Saitoh, Y., Ichihara, A., Tomita, Y., and Nakamura, T. (1991) Biochem. Biophys. Res. Commun. 174, 831 - 838)。为研究HGF是否参与肾脏再生,我们检测了大鼠单侧肾切除或用四氯化碳(CCl4)处理后,肾脏中HGF mRNA、HGF活性和HGF受体的变化。在完整肾脏中,单侧肾切除后6小时HGF mRNA显著增加并达到最大值,随后术后12小时HGF活性增加。在用CCl4处理的大鼠肾脏中也发现了HGF mRNA和HGF活性的显著增加。原位杂交结果表明,肾脏中产生HGF的细胞是内皮细胞。单侧肾切除后12小时,肾细胞膜上HGF受体数量降至正常值的30%,Kd值无变化。术后24小时HGF受体大量减少,术后1周明显恢复至正常水平的60%。由于HGF结合的减少可能是HGF受体内化所致,HGF可能在体内与其受体结合并作为肾上皮细胞的促分裂原。HGF可能在肾损伤后的肾脏再生过程中作为促肾生长因子发挥作用。