Yokoyama-Hayashi Keiko, Takahashi Tsuyoshi, Kakita Akira, Yamashina Shohei
Departments of Surgery, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Endocr J. 2002 Feb;49(1):61-74. doi: 10.1507/endocrj.49.61.
The expression of protein gene product 9.5 (PGP9.5), a known neuron marker, was immunohistochemically investigated in rat pancreas. In fetal pancreas, a cluster of cells expressed PGP9.5 among the initial epithelial buds at embryonic day 11.5 (E 11.5). At E 13.5, PGP9.5 appeared among elongated and branching epithelial cells as well as along nerve fibers in the mesenchyme. On E 17.5, tubular cells became ductal cells with lumen, which strongly expressed PGP9.5. In newborn rats, ductal cells of the common bile duct (CBD) to the centroacinar cells and islet cells expressed PGP9.5. Ten days after birth, the number of the ductal cells expressing PGP9.5 was reduced, and PGP9.5-negative cells appeared in half of the duct cells. On day 21, all centroacinar cells and intercalated ductal cells became PGP9.5-negative, but some CBD and interlobular ductal cells remained positive for PGP9.5. On day 28 and thereafter, PGP9.5 was no longer detected. In a pancreatic duct ligation model, acinar cells changed to cells with duct-like structure after duct ligation. These cells strongly expressed PGP9.5 on the fifth day after duct ligation. Three to four weeks after ligation, the cells with duct-like structure changed to acinar cells, islets of Langerhans and ductal cells, but the ductal cells were PGP9.5-negative at this point. These results suggested that PGP9.5 is expressed in ductal cells that possess a potential for differentiation to pancreatic endocrine cells, and therefore can serve as a marker for the progenitor of pancreatic endocrine cells.
采用免疫组织化学方法,对大鼠胰腺中已知的神经元标志物——蛋白基因产物9.5(PGP9.5)的表达情况进行了研究。在胚胎胰腺中,胚胎第11.5天(E 11.5)时,在最初的上皮芽中出现了一群表达PGP9.5的细胞。E 13.5时,PGP9.5出现在伸长且分支的上皮细胞中,以及间充质中的神经纤维上。E 17.5时,管状细胞变成了有管腔的导管细胞,这些细胞强烈表达PGP9.5。在新生大鼠中,胆总管(CBD)的导管细胞至腺泡中心细胞和胰岛细胞均表达PGP9.5。出生后10天,表达PGP9.5的导管细胞数量减少,半数导管细胞中出现了PGP9.5阴性细胞。第21天时,所有腺泡中心细胞和闰管细胞均变为PGP9.5阴性,但一些CBD和小叶间导管细胞仍为PGP9.5阳性。第28天及以后,未再检测到PGP9.5。在胰腺导管结扎模型中,腺泡细胞在导管结扎后转变为具有导管样结构的细胞。这些细胞在导管结扎后第5天强烈表达PGP9.5。结扎后3至4周,具有导管样结构的细胞转变为腺泡细胞、胰岛细胞和导管细胞,但此时导管细胞为PGP9.5阴性。这些结果表明,PGP9.5在具有向胰腺内分泌细胞分化潜能的导管细胞中表达,因此可作为胰腺内分泌细胞祖细胞的标志物。