Wakayama Tomohiko, Hamada Koichi, Yamamoto Miyuki, Suda Toshio, Iseki Shoichi
Department of Histology and Embryology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, 920-8640 Kanazawa, Japan.
Histochem Cell Biol. 2003 May;119(5):355-62. doi: 10.1007/s00418-003-0528-1. Epub 2003 May 8.
The platelet endothelial cell adhesion molecule-1 (PECAM-1), or CD31, a member of the immunoglobulin superfamily, is located on the plasma membrane of endothelial and hematopoietic cells and involved in vascular development and inflammation. In this study, by use of immunohistochemistry at light and electron microscopic levels in combination with enzyme histochemistry for alkaline phosphatase, we demonstrated that PECAM-1/CD31 is expressed in the mouse primordial germ cell (PGC). Up to 8 days postcoitum (dpc), PGCs with alkaline phosphatase activity showed no PECAM-1/CD31 immunoreactivity. At 9 dpc, PECAM-1/CD31 immunoreactivity was first detected with low intensity in some PGCs located in the hindgut. Between 10 and 11 dpc, intense immunoreactivity was shown on the entire surface of PGCs migrating along the dorsal wall. After arrival and settlement of PGCs in the genital ridges around 11.5 dpc, the intense immunoreactivity was maintained on the entire surface of PGCs. By electron microscopy, the immunoreactivity was localized exclusively on the plasma membrane of PGCs, being as strong at the portions adjacent to neighboring PGCs as those adjacent to somatic cells. As the male and female gonads began to differentiate, PECAM-1/CD31 immunoreactivity remained strong in germ cells until 13 dpc, after which it gradually decreased in intensity and disappeared by 16 dpc. These results suggested that cell-to-cell interaction through PECAM-1/CD31 plays roles in the development of PGCs during their migration on the dorsal wall and homing in the gonads.
血小板内皮细胞黏附分子-1(PECAM-1),即CD31,是免疫球蛋白超家族的成员,位于内皮细胞和造血细胞的质膜上,参与血管发育和炎症反应。在本研究中,我们通过光镜和电镜水平的免疫组织化学结合碱性磷酸酶的酶组织化学方法,证明PECAM-1/CD31在小鼠原始生殖细胞(PGC)中表达。在合子期后8天(dpc)之前,具有碱性磷酸酶活性的PGC未显示PECAM-1/CD31免疫反应性。在9 dpc时,首次在位于后肠的一些PGC中检测到低强度的PECAM-1/CD31免疫反应性。在10至11 dpc之间,沿着背壁迁移的PGC的整个表面呈现强烈的免疫反应性。在约11.5 dpc时PGC到达并定居在生殖嵴后,PGC的整个表面仍保持强烈的免疫反应性。通过电子显微镜观察,免疫反应性仅定位在PGC的质膜上,在与相邻PGC相邻的部分和与体细胞相邻的部分一样强。随着雄性和雌性性腺开始分化,PECAM-1/CD31免疫反应性在生殖细胞中一直保持强烈,直到13 dpc,之后强度逐渐降低,到16 dpc时消失。这些结果表明,通过PECAM-1/CD31的细胞间相互作用在PGC沿背壁迁移和归巢到性腺的过程中发挥作用。