4.7 Article

PDGF signaling from pharyngeal pouches promotes arch artery morphogenesis

Journal

JOURNAL OF GENETICS AND GENOMICS
Volume 46, Issue 12, Pages 551-559

Publisher

SCIENCE PRESS
DOI: 10.1016/j.jgg.2019.11.004

Keywords

PDGF alpha a; PDGF alpha b; Pharyngeal pouch; Pharyngeal arch artery; Tissue-tissue interaction; Zebrafish

Funding

  1. National Natural Science Foundation of China [91739101, 81921006]
  2. National Key Research and Development Program of China [2016YFA0100503, 2018YFA0800200]
  3. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA16000000]

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The great vessels of the heart originate from the pharyngeal arch arteries (PAAs). Anomalies of the PAAs often occur together with pharyngeal pouch malformations, but the reasons for this phenomenon are not fully understood. In the current study, we show that platelet-derived growth factor (PDGF) signaling derived from the pharyngeal pouches plays an important function in PAA vasculogenesis. During PAA development in zebrafish embryos, pdgf alpha a and pdgfab are expressed in the developing pharyngeal pouches. Results from loss-of-function experiments revealed a critical role of these genes in PAA formation. We found that nitroreductase (NTR)-mediated pouch ablation distinctly decreased PDGF receptor tyrosine phosphorylation, yielding a severe loss of PAAs. Importantly, pouch-specific overexpression of pdgf alpha a in pdgf alpha a(-/-); pdgf alpha b(-/-) mutants significantly relieved the PAA defects, which indicated a primary role of pharyngeal pouch-expressed PDGF ligands in signal activation and PAA morphogenesis. Our findings further showed that PDGF signaling was indispensable for the proliferation of PAA angioblasts. Together, these results established a role for PDGF alpha a- and PDGF alpha b-mediated tissue-tissue interaction during PAA development. Copyright (C) 2019, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China. Published by Elsevier Limited and Science Press. All rights reserved.

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