Type IV collagen drives alveolar epithelial–endothelial association and the morphogenetic movements of septation

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Type IV collagen drives alveolar epithelial–endothelial association and the morphogenetic movements of septation

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Title: Type IV collagen drives alveolar epithelial–endothelial association and the morphogenetic movements of septation
Author: Loscertales, Maria; Nicolaou, Fotini; Jeanne, Marion; Longoni, Mauro; Gould, Douglas B.; Sun, Yunwei; Maalouf, Faouzi I.; Nagy, Nandor; Donahoe, Patricia K.

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Citation: Loscertales, Maria, Fotini Nicolaou, Marion Jeanne, Mauro Longoni, Douglas B. Gould, Yunwei Sun, Faouzi I. Maalouf, Nandor Nagy, and Patricia K. Donahoe. 2016. “Type IV collagen drives alveolar epithelial–endothelial association and the morphogenetic movements of septation.” BMC Biology 14 (1): 59. doi:10.1186/s12915-016-0281-2. http://dx.doi.org/10.1186/s12915-016-0281-2.
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Abstract: Background: Type IV collagen is the main component of the basement membrane that gives strength to the blood–gas barrier (BGB). In mammals, the formation of a mature BGB occurs primarily after birth during alveologenesis and requires the formation of septa from the walls of the saccule. In contrast, in avians, the formation of the BGB occurs rapidly and prior to hatching. Mutation in basement membrane components results in an abnormal alveolar phenotype; however, the specific role of type IV collagen in regulating alveologenesis remains unknown. Results: We have performed a microarray expression analysis in late chick lung development and found that COL4A1 and COL4A2 were among the most significantly upregulated genes during the formation of the avian BGB. Using mouse models, we discovered that mutations in murine Col4a1 and Col4a2 genes affected the balance between lung epithelial progenitors and differentiated cells. Mutations in Col4a1 derived from the vascular component were sufficient to cause defects in vascular development and the BGB. We also show that Col4a1 and Col4a2 mutants displayed disrupted myofibroblast proliferation, differentiation and migration. Lastly, we revealed that addition of type IV collagen protein induced myofibroblast proliferation and migration in monolayer culture and increased the formation of mesenchymal–epithelial septal-like structures in co-culture. Conclusions: Our study showed that type IV collagen and, therefore the basement membrane, play fundamental roles in coordinating alveolar morphogenesis. In addition to its role in the formation of epithelium and vasculature, type IV collagen appears to be key for alveolar myofibroblast development by inducing their proliferation, differentiation and migration throughout the developing septum. Electronic supplementary material The online version of this article (doi:10.1186/s12915-016-0281-2) contains supplementary material, which is available to authorized users.
Published Version: doi:10.1186/s12915-016-0281-2
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942891/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:27822273
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