鹌鹑
生物
SOX2
胚胎干细胞
性腺
同源盒蛋白纳米
胚胎
细胞生物学
男科
胚胎发生
分子生物学
遗传学
解剖
内分泌学
诱导多能干细胞
基因
医学
作者
Saeed Yakhkeshi,Shaban Rahimi,Mouhsen Sharafi,Seyedeh‐Nafiseh Hassani,G Shahverdi,Hossein Baharvand
标识
DOI:10.1093/jas/sky404.779
摘要
Primordial germ cells (PGCs), the precursors of ova and spermatozoa are ideal tools for transgenic technology. Therefore isolation, characterization and migration of PGCs is required. The quail has been proven to be a good model in numerous fields of research, especially for biotechnology due to short generation time. In this study, initially we attempted to isolate quail PGCs from gonad (at stage 28–30) and blood (at stage 13–15) as two sources of these cells. The isolated PGC were cultured on feeder cells derived from chicken embryonic fibroblast. Then characterization of these cells were evaluated during the culture. In finally for migration assay of these cells into the gonads, cultured PGCs were injected into blood circulate of the recipients quail embryos. The cultured gonadal PGC proliferated about 400-times versus 100-times in blood PGC during the first 40–50 days. The identities of the PGC were confirmed using periodic acid-Schiff (PAS) staining or anti-SSEA1, β-Catenin, β-integrin, and Nanog immunofluorescence staining or reverse transcription-polymerase chain reaction for several factors related to PGC phenotype, DAZL, PRDM14, VASA and Sox2. Cultured PGCs migrated toward the embryonic gonads when they were transplanted into the blood circulate of the recipient embryo at stage 13–15 Hamburger–Hamilton (HH). Our results suggest that cultured PGCs retain their ability to migrate and colonize the gonads of recipient embryos.
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