Orth J M, Jester W F, Qiu J
Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
Mol Reprod Dev. 1996 Oct;45(2):123-31. doi: 10.1002/(SICI)1098-2795(199610)45:2<123::AID-MRD3>3.0.CO;2-V.
Information gathered from mutant mouse models and from studies on normal puberal and adult animals points to the product of the c-kit gene, a tyrosine kinase surface receptor, and the kit-ligand (KL) as important for gametogenesis in males. In fetuses, KL serves as a survival factor for primordial germ cells, at least in vitro, and in adults activity of the c-kit gene has been indirectly related to survival and subsequent development of differentiating spermatogonia. However, because of the structural complexity of the seminiferous epithelium in adults, c-kit mRNA has not yet been definitively localized to one or more types of spermatogenic cells. In addition, no information is currently available regarding the possible involvement of the c-kit protein and its ligand in mediating germ cell development and/or Sertoli-germ cell interactions immediately after birth when events critical for later onset of spermatogenesis are ongoing. Thus, the aims of the current study were (1) to determine whether the c-kit gene is expressed in testes of neonatal and adult rats and, if so, by what specific cell types, and (2) to determine if those cells expressing the gene also produce the c-kit receptor protein. For this, we isolated total RNA from testes of pups aged days 1-5 and from adult rat testes, and probed for the presence of c-kit mRNA with Northern analysis. We identified the cells containing the c-kit message by carrying out in situ hybridization with digoxigenin-labeled probes, thus allowing the colorimetric signal to be assigned beyond doubt to individual cells in sections of testes. We also utilized Western analysis and immunolocalization to confirm the presence of the c-kit receptor protein in testes at these ages and to identify those cells types producing it. Our findings indicate that (1) neonatal gonocytes express the c-kit gene and produce the receptor protein on postnatal days 1 through 5, spanning the time when they resume dividing and migrating, and (2) spermatogonia and, to a lesser extent, spermatocytes and spermatids of adults express the gene but c-kit protein is present in detectable amounts only in spermatogonia and possibly a few early primary spermatocytes.
从突变小鼠模型以及对正常青春期和成年动物的研究中收集到的信息表明,c-kit基因(一种酪氨酸激酶表面受体)的产物以及kit配体(KL)对雄性配子发生很重要。在胎儿中,KL至少在体外作为原始生殖细胞的存活因子,而在成年动物中,c-kit基因的活性已间接与分化中的精原细胞的存活和后续发育相关。然而,由于成年动物生精上皮的结构复杂性,c-kit mRNA尚未明确定位于一种或多种生精细胞类型。此外,目前尚无关于c-kit蛋白及其配体在出生后即生精过程后期关键事件正在进行时,可能参与介导生殖细胞发育和/或支持细胞-生殖细胞相互作用的信息。因此,本研究的目的是:(1)确定c-kit基因是否在新生和成年大鼠的睾丸中表达,如果表达,是由哪些特定细胞类型表达;(2)确定那些表达该基因的细胞是否也产生c-kit受体蛋白。为此,我们从1-5日龄幼鼠的睾丸和成年大鼠的睾丸中分离出总RNA,并用Northern分析检测c-kit mRNA的存在。我们通过用洋地黄毒苷标记的探针进行原位杂交来鉴定含有c-kit信息的细胞,从而使比色信号能够明确地归因于睾丸切片中的单个细胞。我们还利用Western分析和免疫定位来确认这些年龄段睾丸中c-kit受体蛋白的存在,并鉴定产生该蛋白的细胞类型。我们的研究结果表明:(1)新生生殖母细胞在出生后1至5天表达c-kit基因并产生受体蛋白,这一时期涵盖了它们恢复分裂和迁移的时间;(2)成年动物的精原细胞以及程度较轻的精母细胞和精子细胞表达该基因,但c-kit蛋白仅在精原细胞以及可能的少数早期初级精母细胞中以可检测的量存在。