Volume 86, Issue 12 p. 1810-1821
RESEARCH ARTICLE

Enrichment of transplantable germ cells in salmonids using a novel monoclonal antibody by magnetic‐activated cell sorting

Kensuke Ichida

School of Animal Production Technology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima, Thailand

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Makoto Hayashi

Life Science Center for Survival Dynamics, Tsukuba Advanced Research Alliance, University of Tsukuba, Ibaraki, Japan

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Misako Miwa

Department of Marine Biosciences, Tokyo University of Marine Science and Technology, Tokyo, Japan

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Ryota Kitada

Department of Marine Biosciences, Tokyo University of Marine Science and Technology, Tokyo, Japan

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Momo Takahashi

Department of Marine Biosciences, Tokyo University of Marine Science and Technology, Tokyo, Japan

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Ryo Fujihara

Department of Marine Biosciences, Tokyo University of Marine Science and Technology, Tokyo, Japan

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Surintorn Boonanuntanasarn

School of Animal Production Technology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima, Thailand

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Goro Yoshizaki

Corresponding Author

Department of Marine Biosciences, Tokyo University of Marine Science and Technology, Tokyo, Japan

Correspondence Goro Yoshizaki, Department of Marine Biosciences, Tokyo University of Marine Science and Technology, 4‐5‐7 Konan, Minato‐ku, Tokyo 108‐8477, Japan.

Email: goro@kaiyodai.ac.jp

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First published: 23 September 2019
Citations: 4

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 vasagfp 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.

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