Type VI collagen is proportionally lower around airways and blood vessels in idiopathic pulmonary fibrosis
Helene Wallem Breisnes, Mehmet Nizamoglu, Maunick Lefin Koloko Ngassie, Theo Borghuis, Marnix R. Jonker, Rhode A. Meuleman, Tessa Kole, Corry‐Anke Brandsma, Simon Francis Thomsen, M.A. Karsdal, Diana Julie Leeming, Filipa Bica Simões, Jannie Marie Bülow Sand, Janette Kay Burgess
The paper shows that in IPF lungs, COL6 gene expression is higher but protein levels and synthesis around airways and vessels are lower, suggesting disrupted matrix organization and fibroblast persistence.
American Journal of Physiology-Cell Physiology · Sep 15, 2026Peer-reviewedMolecular Biology