| Literature DB >> 31544311 |
Kensuke Ichida1, Makoto Hayashi2, Misako Miwa3, Ryota Kitada3, Momo Takahashi3, Ryo Fujihara3, Surintorn Boonanuntanasarn1, Goro Yoshizaki3.
Abstract
In the fish germ cell transplantation system, only type A spermatogonia (ASGs) and oogonia are known to be incorporated into the recipient genital ridges, where they undergo gametogenesis. Therefore, high colonization efficiency can be achieved by enriching undifferentiated germ cells out of whole testicular cells. In this study, we used magnetic-activated cell sorting (MACS) for enriching undifferentiated germ cells of rainbow trout using a monoclonal antibody that recognizes a specific antigen located on the germ cell membrane. We screened the antibodies to be used for MACS by performing immunohistochemistry on rainbow trout gonads. Two antibodies, nos. 172 and 189, showed strong signals for ASGs and oogonia. Next, we performed MACS with antibody no. 172 using gonadal cells isolated from vasa-gfp rainbow trout showing GFP in undifferentiated germ cells. We found that GFP-positive cells are highly enriched in antibody no. 172-positive fractions. Finally, to examine the transplantability of MACS-enriched cells, we intraperitoneally transplanted sorted or unsorted cells into recipient larvae. We observed that transplantability of sorted cells, particularly ovarian cells, were significantly higher than that of unsorted cells. Therefore, MACS with antibody no. 172 could enrich ASGs and oogonia and become a powerful tool to improve transplantation efficiency in salmonids.Entities:
Keywords: germ cell transplantation; magnetic-activated cell sorting; oogonia; salmonid; spermatogonia
Year: 2019 PMID: 31544311 DOI: 10.1002/mrd.23275
Source DB: PubMed Journal: Mol Reprod Dev ISSN: 1040-452X Impact factor: 2.609