Attaining proper organ size during development and regeneration hinges on the activity of mitogenic factors. Here, we performed a large-scale chemical screen in embryonic zebrafish to identify cardiomyocyte mitogens. Although commonly considered antiproliferative, vitamin D analogs like alfacalcidol had rapid, potent mitogenic effects on embryonic and adult cardiomyocytes in vivo. Moreover, pharmacologic or genetic manipulation of vitamin D signaling controlled proliferation in multiple adult cell types and dictated growth rates in embryonic and juvenile zebrafish. Tissue-specific modulation of vitamin D receptor (VDR) signaling had organ-restricted effects, with cardiac VDR activation causing cardiomegaly. Alfacalcidol enhanced the regenerative response of injured zebrafish hearts, whereas VDR blockade inhibited regeneration. Alfacalcidol activated cardiac expression of genes associated with ErbB2 signaling, while ErbB2 inhibition blunted its effects on cell proliferation. Our findings identify vitamin D as mitogenic for cardiomyocytes and other cell types in zebrafish and indicate a mechanism to regulate organ size and regeneration.
Journal article
Vitamin D Stimulates Cardiomyocyte Proliferation and Controls Organ Size and Regeneration in Zebrafish
Developmental Cell, Vol.48(6), pp.853-863.e5
25/Mar/2019
Abstract
Details
- Title
- Vitamin D Stimulates Cardiomyocyte Proliferation and Controls Organ Size and Regeneration in Zebrafish
- Creators
- Yanchao Han (null) - Duke UniversityAnzhi Chen (null) - Duke UniversityKfir-Baruch Umansky (null) - 972WIS_INST___122Kelsey A. Oonk (null) - Duke UniversityWen-Yee Choi (null) - Duke UniversityAmy L. Dickson (null) - Duke UniversityJianhong Ou (null) - Duke UniversityValentina Cigliola (null) - Duke UniversityOren Yifa (null) - 972WIS_INST___122Jingli Cao (null) - Duke UniversityValerie A. Tornini (null) - Duke UniversityBen D. Cox (null) - Duke UniversityEldad Tzahor (null) - 972WIS_INST___122Kenneth D. Poss (Corresponding Author) - Duke University
- Resource Type
- Journal article
- Publication Details
- Developmental Cell, Vol.48(6), pp.853-863.e5; 25/Mar/2019
- Number of pages
- 16
- Language
- English
- DOI
- https://doi.org/10.1016/j.devcel.2019.01.001
- Grant note
- We thank Duke Zebrafish Core Facilities staff for zebrafish care; Duke Computing Cluster for computing support; Duke University Proteomics and Metabolomics Core Facility for metabolomics analysis; A. Arnold for PS121912; J. Rawls and B. Link for DNA constructs; M. Bagnat, M. Goll, and D. Shin for zebrafish lines; R. Karra and N. Bursac for discussions; and J. Kang for comments on the manuscript. This work was supported by predoctoral fellowships from the American Heart Association (AHA) to A.C. and the National Science Foundation to V.A.T. and B.D.C.; postdoctoral fellowships from AHA to J.C., from the Swiss National Science Foundation to V.C., and from the National Institutes of Health (NIH) to W.-Y.C.; grants from the NIH (R01 HL081674, R01 GM074057, R01 HL136182, and R01 HL131319), the March of Dimes, and the AHA to K.D.P.; and a grant from Fondation Leducq to K.D.P. and E.T. Author Contributions Conceptualization, Y.H., W.-Y.C., and K.D.P.; Methodology, Y.H., W.-Y.C., and K.-B.U.; Investigation, Y.H., A.C., K.-B.U., K.A.O., W.-Y.C., A.L.D., and O.Y.; Writing – Original Draft, Y.H., K.-B.U., and K.D.P.; Writing – Review & Editing, Y.H. and K.D.P.; Funding Acquisition, A.C., V.A.T., B.D.C., J.C., V.C., W.-Y.C., E.T., and K.D.P.; Resources, Y.H., A.C., K.A.O., V.C., J.C., V.A.T., and B.D.C.; Visualization, Y.H. and J.O.; Supervision, K.D.P. and E.T.
- Record Identifier
- 993262354203596
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