Zbinden Aline, Layland Shannon L, Urbanczyk Max, Carvajal Berrio Daniel A, Marzi Julia, Zauner Monika, Hammerschmidt Anne, Brauchle Eva M, Sudrow Katrin, Fink Simon, Templin Markus, Liebscher Simone, Klein Gerd, Deb Arjun, Duffy Garry P, Crooks Gay M, Eble Johannes A, Mikkola Hanna K A, Nsair Ali, Seifert Martina, Schenke-Layland Katja
Department of Bioengineering Eberhard Karls University Tübingen Tübingen 72076 Germany.
Department of Women's Health Research Institute for Women's Health Eberhard Karls University Tübingen Tübingen 72076 Germany.
Adv Sci (Weinh). 2020 Dec 21;8(4):2002500. doi: 10.1002/advs.202002500. eCollection 2021 Feb.
Ischemia impacts multiple organ systems and is the major cause of morbidity and mortality in the developed world. Ischemia disrupts tissue homeostasis, driving cell death, and damages tissue structure integrity. Strategies to heal organs, like the infarcted heart, or to replace cells, as done in pancreatic islet -cell transplantations, are often hindered by ischemic conditions. Here, it is discovered that the basement membrane glycoprotein nidogen-1 attenuates the apoptotic effect of hypoxia in cardiomyocytes and pancreatic -cells via the v3 integrin and beneficially modulates immune responses in vitro. It is shown that nidogen-1 significantly increases heart function and angiogenesis, while reducing fibrosis, in a mouse postmyocardial infarction model. These results demonstrate the protective and regenerative potential of nidogen-1 in ischemic conditions.
缺血会影响多个器官系统,是发达国家发病和死亡的主要原因。缺血会破坏组织稳态,导致细胞死亡,并损害组织结构完整性。修复器官(如梗死心脏)或替换细胞(如胰岛细胞移植)的策略常常受到缺血条件的阻碍。在此,研究发现基底膜糖蛋白巢蛋白-1通过整合素v3减轻缺氧对心肌细胞和胰腺细胞的凋亡作用,并在体外对免疫反应产生有益调节。研究表明,在小鼠心肌梗死后模型中,巢蛋白-1可显著增强心脏功能和血管生成,同时减少纤维化。这些结果证明了巢蛋白-1在缺血条件下的保护和再生潜力。