TY - JOUR
T1 - Visualization and tracking of live type a spermatogonia using a fluorescence-conjugated antibody in Salmo species
AU - Ichida, Kensuke
AU - Matsushita, Yoshiyuki
AU - Amano, Yuichi
AU - Miwa, Misako
AU - Nagasawa, Kazue
AU - Hayashi, Makoto
AU - Mizutani, Hanaka
AU - Takahashi, Momo
AU - Boonanuntanasarn, Surintorn
AU - Yoshizaki, Goro
N1 - Funding Information:
We gratefully acknowledge Prof. Igor Babiak, Cesilie Røtnes Amundsen, Joanna Babiak, Komeil Razmi (Faculty of Biosciences and Aquaculture, Nord University, N-8049 Bodø, Norway) for kindly providing Atlantic salmon testes. This work was supported by a Grant-in-Aid for Scientific Research (KAKENHI) on Innovative Areas, “Establishment of gamete integrity (18H05545),” Research and Development Program for Future Creation (18077249) from JST, and Ocean Resource Use Promotion Technology Development Program from MEXT (to G.Y.).
Funding Information:
We gratefully acknowledge Prof. Igor Babiak, Cesilie Røtnes Amundsen, Joanna Babiak, Komeil Razmi (Faculty of Biosciences and Aquaculture, Nord University, N-8049 Bodø, Norway) for kindly providing Atlantic salmon testes. This work was supported by a Grant-in-Aid for Scientific Research (KAKENHI) on Innovative Areas, “Establishment of gamete integrity (18H05545),” Research and Development Program for Future Creation (18077249) from JST, and Ocean Resource Use Promotion Technology Development Program from MEXT (to G.Y.).
Publisher Copyright:
© 2020
PY - 2021/2/25
Y1 - 2021/2/25
N2 - Combining germ cell cryopreservation with transplantation is a powerful tool for preserving the genetic resources of various fish strains. In this germ cell transplantation system, since only type A spermatogonia (ASGs) among the various testicular cells have the potency to colonize recipient gonads and resume gametogenesis, techniques for visualization, isolation, and tracing of ASGs facilitate ease of manipulation. Here we established an ASG visualization technique in two Salmo species: brown trout and Atlantic salmon. We applied a monoclonal antibody (antibody No. 95), which specifically recognizes a cell surface antigen of ASGs obtained from rainbow trout, against Salmo species. Immunohistochemistry studies showed that antibody No. 95 also specifically detected the ASGs of brown trout and Atlantic salmon. Furthermore, marker-gene analyses of brown trout testicular cells sorted by flow cytometry using Alexa flour 488-conjugated antibody No. 95 revealed that fluorescent-positive cells possessed molecular characteristics of ASGs. Finally, to investigate the transplantability of antibody-positive cells, ASGs pre-stained with antibody No. 95 were transplanted into the peritoneal cavity of rainbow trout larvae. As a result, fluorescent cells incorporated into the recipient gonads, suggesting that the visualized ASGs possess transplantability. Thus, it is expected that the ASG visualization methods developed in this study will facilitate the development of more efficiency of germ cell transplantation techniques in Salmo species.
AB - Combining germ cell cryopreservation with transplantation is a powerful tool for preserving the genetic resources of various fish strains. In this germ cell transplantation system, since only type A spermatogonia (ASGs) among the various testicular cells have the potency to colonize recipient gonads and resume gametogenesis, techniques for visualization, isolation, and tracing of ASGs facilitate ease of manipulation. Here we established an ASG visualization technique in two Salmo species: brown trout and Atlantic salmon. We applied a monoclonal antibody (antibody No. 95), which specifically recognizes a cell surface antigen of ASGs obtained from rainbow trout, against Salmo species. Immunohistochemistry studies showed that antibody No. 95 also specifically detected the ASGs of brown trout and Atlantic salmon. Furthermore, marker-gene analyses of brown trout testicular cells sorted by flow cytometry using Alexa flour 488-conjugated antibody No. 95 revealed that fluorescent-positive cells possessed molecular characteristics of ASGs. Finally, to investigate the transplantability of antibody-positive cells, ASGs pre-stained with antibody No. 95 were transplanted into the peritoneal cavity of rainbow trout larvae. As a result, fluorescent cells incorporated into the recipient gonads, suggesting that the visualized ASGs possess transplantability. Thus, it is expected that the ASG visualization methods developed in this study will facilitate the development of more efficiency of germ cell transplantation techniques in Salmo species.
KW - Atlantic salmon
KW - Brown trout
KW - Cell surface antigen
KW - Monoclonal antibody
KW - Spermatogonia
UR - http://www.scopus.com/inward/record.url?scp=85095859691&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85095859691&partnerID=8YFLogxK
U2 - 10.1016/j.aquaculture.2020.736096
DO - 10.1016/j.aquaculture.2020.736096
M3 - Article
AN - SCOPUS:85095859691
SN - 0044-8486
VL - 533
JO - Aquaculture
JF - Aquaculture
M1 - 736096
ER -