Matrix biology : journal of the International Society for Matrix Biology · 2016
Ltbp4 regulates Pdgfrβ expression via TGFβ-dependent modulation of Nrf2 transcription factor function.
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Tomasovic Ana, Kurrle Nina, Wempe Frank, De-Zolt Silke, Scheibe Susan, Koli Katri, Serchinger Martin, Schnütgen Frank, Sürün Duran, Sterner-Kock Anja, Weissmann Norbert, von Melchner Harald
Аннотация
Latent transforming growth factor beta binding protein 4 (LTBP4) belongs to the fibrillin/LTBP family of proteins and plays an important role as a structural component of extracellular matrix (ECM) and local regulator of TGFβ signaling. We have previously reported that Ltbp4S knock out mice (Ltbp4S-/-) develop centrilobular emphysema reminiscent of late stage COPD, which could be partially rescued by inactivating the antioxidant protein Sestrin 2 (Sesn2). More recent studies showed that Sesn2 knock out mice upregulate Pdgfrβ-controlled alveolar maintenance programs that protect against cigarette smoke induced pulmonary emphysema. Based on this, we hypothesized that the emphysema of Ltbp4S-/- mice is primarily caused by defective Pdgfrβ signaling. Here we show that LTBP4 induces Pdgfrβ signaling by inhibiting the antioxidant Nrf2/Keap1 pathway in a TGFβ-dependent manner. Overall, our data identified Ltbp4 as a major player in lung remodeling and injury repair.
Предметные рубрики MeSH
AnimalsCell LineEpithelial CellsExtracellular MatrixFibroblastsGene Expression RegulationKelch-Like ECH-Associated Protein 1Latent TGF-beta Binding ProteinsLungMiceMice, KnockoutMinkNF-E2-Related Factor 2Nuclear ProteinsPeroxidasesPlasmidsPulmonary EmphysemaReceptor, Platelet-Derived Growth Factor betaSignal TransductionTransforming Growth Factor betaTropoelastinSestrins