Analysis of the function of ADAM17 in iRhom2 curlyoare and tylosis with esophageal cancer mutant mice

Rabinowitsch, Ariana I.; Maretzky, Thorsten; Weskamp, Gisela; Haxaire, Coline; Tueshaus, Johanna; Lichtenthaler, Stefan F.; Monette, Sebastien und Blobei, Carl P. (2023): Analysis of the function of ADAM17 in iRhom2 curlyoare and tylosis with esophageal cancer mutant mice. In: Journal of Cell Science, Bd. 136, Nr. 13, jcs260910

Abstract

Tylosis with oesophageal cancer (TOC) is a rare familial disordercaused by cytoplasmic mutations in inactiv e rhomboid 2 (iRhom2 or iR2, encoded by Rhbdf2). iR2 and the related iRhom1 (or iR1, encoded by Rhbdf1) are key regulators of the membrane-anchored metalloprotease ADAM17, which is required for activating EGFR ligands and for releasing pro-inflammatory cytokines such as TNF & alpha;(or TNF). A cytoplasmic deletion in iR2, including the TOC site, leads to curly coat or bare skin (cub) in mice, whereas a knock-in TOC mutation (toc) causes less severe alopecia and wavy fur. The abnormal skin and hair phenotypes of iR2cu b / c u b and iR2toc/toc mice depend on amphiregulin (Areg) and Adam 17, as loss of one allele of either gene rescues the fur phenotypes. Remarkably, we found that iR1-/- iR2cub/cub mice survived, despite a lack of mature ADAM17, whereas iR2cub/cub Adam17-/- mice died perinatally, suggesting that the iR2cub gain-of-function mutation requires the presence of ADAM17, but not its catalytic activity. The iR2toc mutation did not substantially reduce the levels of mature ADAM17, but instead affected its function in a substrate-selectiv e manner. Our findings provide new insights into the role of the cytoplasmic domain of iR2 in vivo, with implications for the treatment of TOC patients.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Medizin > Munich Cluster for Systems Neurology (SyNergy)
• Themengebiete: 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit
• Sprache: Englisch
• DFG: Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 390857198