Eskild W, Ree A H, Levy F O, Jahnsen T, Hansson V
Institute of Medical Biochemistry, University of Oslo, Norway.
Biol Reprod. 1991 Jan;44(1):53-61. doi: 10.1095/biolreprod44.1.53.
In the present study we have examined the cellular localization and developmental changes of mRNAs for retinoid-binding proteins in rat testis. We demonstrate that mRNA (0.7 kb) for cellular retinol-binding protein (CRBP) is expressed only in Sertoli cells and peritubular cells. The mRNA for CRBP could not be detected in other testicular cells. In contrast, mRNA for cellular retinoic acid-binding protein (CRABP) was detected primarily in germ cells and to a small extent in tumor Leydig cells. The mRNA for CRABP in germ cells revealed distinct size heterogeneity and three distinct mRNA species were observed (1.0, 1.8, and 1.9 kb), in contrast to previous data for somatic cells where only the 1.0-kb mRNA has been reported. Messenger RNAs for retinoic acid receptor-alpha (RAR alpha) were detected in both somatic and haploid germ cells. The highest level of RAR alpha was seen in Sertoli cells, round spermatids, and tumor Leydig cells. Lower, but distinct, levels were observed in peritubular cells. Furthermore, we observed germ cell-specific species of RAR alpha mRNA (4 kb and approximately 7 kb). The smallest mRNA for RAR alpha (2.7 kb) in somatic cells was absent in germ cells. The levels of mRNAs for the various retinoid-binding proteins in whole testis obtained from rats of various ages confirmed this cellular localization. The mRNAs for CRBP, the small molecular size (2.7 kb) mRNA for RAR alpha (localized to somatic cells), and the 1-kb mRNA for CRABP showed an age-dependent decrease.(ABSTRACT TRUNCATED AT 250 WORDS)
在本研究中,我们检测了大鼠睾丸中类视黄醇结合蛋白mRNA的细胞定位及发育变化。我们发现,细胞视黄醇结合蛋白(CRBP)的mRNA(0.7 kb)仅在支持细胞和睾丸间质细胞中表达,在其他睾丸细胞中未检测到CRBP的mRNA。相反,细胞视黄酸结合蛋白(CRABP)的mRNA主要在生殖细胞中检测到,在肿瘤性睾丸间质细胞中也有少量表达。生殖细胞中CRABP的mRNA显示出明显的大小异质性,观察到三种不同的mRNA种类(1.0、1.8和1.9 kb),这与之前报道的体细胞中仅存在1.0 kb mRNA的数据不同。视黄酸受体α(RARα)的mRNA在体细胞和单倍体生殖细胞中均有检测到。RARα在支持细胞、圆形精子细胞和肿瘤性睾丸间质细胞中的表达水平最高,在睾丸间质细胞中的表达水平较低但明显。此外,我们还观察到生殖细胞特异性的RARα mRNA种类(4 kb和约7 kb)。体细胞中最小的RARα mRNA(2.7 kb)在生殖细胞中不存在。从不同年龄大鼠获得的整个睾丸中,各种类视黄醇结合蛋白mRNA的水平证实了这种细胞定位。CRBP的mRNA、RARα的小分子大小(2.7 kb)mRNA(定位于体细胞)和CRABP的1 kb mRNA均呈现年龄依赖性下降。(摘要截短于250字)