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      Zebrafish Kit ligands cooperate with erythropoietin to promote erythroid cell expansion

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          Key Points

          • Kit signaling contributes to erythroid cell development and is conserved from fish to man.

          • Ex vivo expansion and self-renewal of zebrafish erythroid progenitors requires addition of recombinant Kitlga.

          Abstract

          Kit ligand (Kitlg) is pleiotropic cytokine with a prominent role in vertebrate erythropoiesis. Although the role of Kitlg in this process has not been reported in Danio rerio (zebrafish), in the present study we show that its function is evolutionarily conserved. Zebrafish possess 2 copies of Kitlg genes (Kitlga and Kitlgb) as a result of whole-genome duplication. To determine the role of each ligand in zebrafish, we performed a series of ex vivo and in vivo gain- and loss-of-function experiments. First, we tested the biological activity of recombinant Kitlg proteins in suspension culture from zebrafish whole-kidney marrow, and we demonstrate that Kitlga is necessary for expansion of erythroid progenitors ex vivo. To further address the role of kitlga and kitlgb in hematopoietic development in vivo, we performed gain-of-function experiments in zebrafish embryos, showing that both ligands cooperate with erythropoietin (Epo) to promote erythroid cell expansion. Finally, using the kita mutant ( kita b5/ b5 or sparse), we show that the Kita receptor is crucial for Kitlga/b cooperation with Epo in erythroid cells. In summary, using optimized suspension culture conditions with recombinant cytokines (Epo, Kitlga), we report, for the first time, ex vivo suspension cultures of zebrafish hematopoietic progenitor cells that can serve as an indispensable tool to study normal and aberrant hematopoiesis in zebrafish. Furthermore, we conclude that, although partial functional diversification of Kit ligands has been described in other processes, in erythroid development, both paralogs play a similar role, and their function is evolutionarily conserved.

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          Author and article information

          Journal
          Blood Adv
          Blood Adv
          bloodoa
          Blood Adv
          Blood Advances
          Blood Advances
          American Society of Hematology (Washington, DC )
          2473-9529
          2473-9537
          8 December 2020
          1 December 2020
          1 December 2020
          : 4
          : 23
          : 5915-5924
          Affiliations
          [1 ]Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic; and
          [2 ]Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA
          Author information
          https://orcid.org/0000-0002-4932-7579
          https://orcid.org/0000-0001-7443-175X
          https://orcid.org/0000-0002-6202-7650
          Article
          PMC7724902 PMC7724902 7724902 2020/ADV2020001700
          10.1182/bloodadvances.2020001700
          7724902
          33259600
          5465a170-ab87-498b-9e94-3b5772aad17f
          © 2020 by The American Society of Hematology
          History
          : 26 February 2020
          : 20 October 2020
          Page count
          Pages: 10
          Categories
          22
          28
          Hematopoiesis and Stem Cells
          Custom metadata
          free

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