Petersen Cecilia, Svechnikov Konstantin, Fröysa Berit, Söder Olle
Department of Woman and Child Health, Paediatric Endocrinology Unit, Astrid Lindgren Children's Hospital, Karolinska Institutet, Stockholm, Sweden.
Cytokine. 2005 Oct 7;32(1):51-9. doi: 10.1016/j.cyto.2005.07.014. Epub 2005 Sep 21.
We have reported earlier that interleukin-1 (IL-1) is a potent growth factor for immature Sertoli cells (somatic cells in the testis required for testicular development and later spermatogenesis) and that this effect is synergistic with the mitogenic effect of follicle-stimulating hormone (FSH). The aim of the present study was to determine whether MAPK pathways are involved in mediating the mitogenic effect of IL-1 on Sertoli cells. Western blotting revealed that IL-1alpha activated p38 MAPK and JNK/SAPK, but not ERK, in Sertoli cells from 8- or 9-day-old rat. The inhibitor of p38 MAPK SB203580 attenuated the IL-1alpha-induced proliferation of Sertoli cells, as assessed by (3)H-thymidine incorporation and supravital staining as well as by direct cell counting. We conclude that the p38 MAPK pathway mediates the proliferative effect of IL-1alpha on immature Sertoli cells in vitro. Since the mitogenic effect of FSH is mediated via ERK, the synergistic action of IL-1alpha and FSH may be explained by their different intracellular signalling pathways. Induction of IL-1 by inflammation, infection or other tissue injuries may result in testicular damage by interfering with normal Sertoli cell development and thus future spermatogenesis.
我们先前曾报道,白细胞介素-1(IL-1)是未成熟支持细胞(睾丸发育及后续精子发生所必需的睾丸体细胞)的一种强效生长因子,且这种作用与促卵泡激素(FSH)的促有丝分裂作用具有协同性。本研究的目的是确定丝裂原活化蛋白激酶(MAPK)通路是否参与介导IL-1对支持细胞的促有丝分裂作用。蛋白质免疫印迹法显示,IL-1α可激活8日龄或9日龄大鼠支持细胞中的p38 MAPK和JNK/SAPK,但不激活细胞外信号调节激酶(ERK)。通过³H-胸腺嘧啶核苷掺入法、超活染色以及直接细胞计数评估发现,p38 MAPK抑制剂SB203580可减弱IL-1α诱导的支持细胞增殖。我们得出结论,p38 MAPK通路在体外介导了IL-1α对未成熟支持细胞的增殖作用。由于FSH的促有丝分裂作用是通过ERK介导的,因此IL-1α与FSH的协同作用可能是由它们不同的细胞内信号通路所解释的。炎症、感染或其他组织损伤诱导产生的IL-1可能会通过干扰支持细胞的正常发育从而影响未来的精子发生,进而导致睾丸损伤。