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Origin and fate of vascular myofibroblasts and smooth muscle cells during pulmonary vascular remodeling and reverse remodeling (A04)

Subject Area Pneumology, Thoracic Surgery
Term since 2016
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 268555672
 
Pulmonary hypertension (PH) is largely present in patients suffering from chronic lung diseases such as COPD. Although current dogma states that PH-associated vascular smooth muscle cells (VSMCs) arise predominantly due to the expansion of pre-existing VSMCs located in the proximal part of pulmonary vessels, we showed that perivascular, sonic-hedgehog-responsive GLI1+ cells are major contributors to VSMCs in both hypoxia and cigarette-smoke-induced PH. In the next funding period, we aim to characterize, genetically manipulate and ablate the specific subset of GLI1+ cells contributing to PH, with special emphasis on FGF signaling in the context of both mouse and human-derived material.
DFG Programme Collaborative Research Centres
Applicant Institution Justus-Liebig-Universität Gießen
 
 

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