Pulmonary Vascular Platform Models the Effects of Flow and Pressure on Endothelial Dysfunction in BMPR2 Associated Pulmonary Arterial Hypertension

Endothelial dysfunction is a known consequence of bone morphogenetic protein type II receptor (BMPR2) mutations seen in pulmonary arterial hypertension (PAH). However, standard 2D cell culture models fail to mimic the mechanical environment seen in the pulmonary vasculature. Hydrogels have emerged a...

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Detalles Bibliográficos
Autores principales: D’Amico, Reid W., Faley, Shannon, Shim, Ha-na, Prosser, Joanna R., Agrawal, Vineet, Bellan, Leon M., West, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164056/
https://www.ncbi.nlm.nih.gov/pubmed/30158434
http://dx.doi.org/10.3390/ijms19092561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164056/
https://www.ncbi.nlm.nih.gov/pubmed/30158434
http://dx.doi.org/10.3390/ijms19092561

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