TY  - JOUR
AU  - Weiden, Eva-Maria
AU  - Serianz, Zala
AU  - Klingl, Yvonne
AU  - Jörs, Simone
AU  - Jaślan, Dawid
AU  - Keller, Marco
AU  - Castro, Sandra Prat
AU  - Mkhitaryan, Mane
AU  - Jeridi, Aicha
AU  - Briukhovetska, Daria
AU  - Spix, Barbara
AU  - Scotto Rosato, Anna
AU  - Agami, Ahmed
AU  - Schiller, Herbert B
AU  - Rajan, Suhasini
AU  - Schredelseker, Johann
AU  - Fois, Giorgio
AU  - Frick, Manfred
AU  - Kobold, Sebastian
AU  - Klein, Margarethe
AU  - Geisler, Fabian
AU  - Garcia-Fortanet, Jorge
AU  - Murphy, Leon O
AU  - Bracher, Franz
AU  - Wahl-Schott, Christian
AU  - Gudermann, Thomas
AU  - Dietrich, Alexander
AU  - Biel, Martin
AU  - Yildirim, Ali Önder
AU  - Grimm, Christian
TI  - TRPML1 suppresses pulmonary fibrosis by limiting collagen and elastin deposition.
JO  - The EMBO journal
VL  - nn
SN  - 0261-4189
CY  - [London]
PB  - Nature Publishing Group UK
M1  - DKFZ-2026-00403
SP  - nn
PY  - 2026
N1  - epub
AB  - In pulmonary fibrosis lung tissue is thickened and scarred, and the lungs become progressively stiffer and smaller, leading to low levels of blood oxygen and shortness of breath. Lung fibrosis is not curable and life expectancy is reduced. Fibrosis is characterized by an increased accumulation of extracellular matrix (ECM) proteins such as collagen and elastin. ECM proteins are degraded predominantly by matrix metalloproteinases (MMPs). Here, we show that the lysosomal cation channel TRPML1, which causes the lysosomal storage disorder mucolipidosis type IV (MLIV) when mutated or lost, regulates the levels of MMPs in the ECM of mouse airways, modulating exocytosis of MMP2, 8, 9, 12, and 19, which mediate collagen/elastin degradation. While TRPML1 loss reduces MMP levels in lung macrophage and fibroblast supernatants, small molecule activation of TRPML1 results in increased levels. MLIV mice display a fibrosis-like lung phenotype similar to the phenotype evoked by bleomycin. We thus identify TRPML1 as a regulator of MMP release in the lung with loss of TRPML1 resulting in lung fibrosis due to excessive extracellular collagen and elastin accumulation.
KW  - Mcoln1 (Other)
KW  - Pulmonary Fibrosis (Other)
KW  - TRPML (Other)
KW  - TRPML1 (Other)
KW  - TRPML3 (Other)
LB  - PUB:(DE-HGF)16
C6  - pmid:41714729
DO  - DOI:10.1038/s44318-026-00712-4
UR  - https://inrepo02.dkfz.de/record/309977
ER  -