Developmental cell · 2021
VEGF receptor 2 (KDR) protects airways from mucus metaplasia through a Sox9-dependent pathway.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Jiang Ming, Fang Yinshan, Li Yu, Huang Huachao, Wei Zichen, Gao Xia, Sung Hoon-Ki, Hu Jim, Qiang Li, Ruan Jian, Chen Qixuan, Jiang Dianhua, Whitsett Jeffrey A, Ai Xingbin, Que Jianwen
Аннотация
Mucus-secreting goblet cells are the dominant cell type in pulmonary diseases, e.g., asthma and cystic fibrosis (CF), leading to pathologic mucus metaplasia and airway obstruction. Cytokines including IL-13 are the major players in the transdifferentiation of club cells into goblet cells. Unexpectedly, we have uncovered a previously undescribed pathway promoting mucous metaplasia that involves VEGFa and its receptor KDR. Single-cell RNA sequencing analysis coupled with genetic mouse modeling demonstrates that loss of epithelial VEGFa, KDR, or MEK/ERK kinase promotes excessive club-to-goblet transdifferentiation during development and regeneration. Sox9 is required for goblet cell differentiation following Kdr inhibition in both mouse and human club cells. Significantly, airway mucous metaplasia in asthmatic and CF patients is also associated with reduced KDR signaling and increased SOX9 expression. Together, these findings reveal an unexpected role for VEGFa/KDR signaling in the defense against mucous metaplasia, offering a potential therapeutic target for this common airway pathology.
Предметные рубрики MeSH
Airway ObstructionAnimalsCell TransdifferentiationDisease Models, AnimalGene Expression RegulationGoblet CellsHumansInterleukin-13MAP Kinase Signaling SystemMetaplasiaMiceMucusSOX9 Transcription FactorSingle-Cell AnalysisVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2