{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,29]],"date-time":"2026-10-29T23:51:54Z","timestamp":1793317914843,"version":"4.5.0"},"reference-count":47,"publisher":"Cold Spring Harbor Laboratory","issue":"23","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Genes Dev."],"published-print":{"date-parts":[[1997,12,1]]},"abstract":"<jats:p>Previous studies suggest that plectin, a versatile cytoskeletal linker protein, has an important role in maintaining the structural integrity of diverse cells and tissues. To establish plectin\u2019s function in a living organism, we have disrupted its gene in mice. Plectin (\u2212\/\u2212) mice died 2\u20133 days after birth exhibiting skin blistering caused by degeneration of keratinocytes. Ultrastructurally, hemidesmosomes and desmosomes appeared unaffected. In plectin-deficient mice, however, hemidesmosomes were found to be significantly reduced in number and apparently their mechanical stability was altered. The skin phenotype of these mice was similar to that of patients suffering from epidermolysis bullosa simplex (EBS)-MD, a hereditary skin blistering disease with muscular dystrophy, caused by defects in the plectin gene. In addition, plectin (\u2212\/\u2212) mice revealed abnormalities reminiscent of minicore myopathies in skeletal muscle and disintegration of intercalated discs in heart. Our results clearly demonstrate a general role of plectin in the reinforcement of mechanically stressed cells. Plectin (\u2212\/\u2212) mice will provide a useful tool for the study of EBS-MD, and possibly other types of plectin-related myopathies involving skeletal and cardiac muscle, in an organism amenable to genetic manipulation.<\/jats:p>","DOI":"10.1101\/gad.11.23.3143","type":"journal-article","created":{"date-parts":[[2008,2,20]],"date-time":"2008-02-20T22:15:26Z","timestamp":1203545726000},"page":"3143-3156","source":"Crossref","is-referenced-by-count":284,"title":["Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart\u2009cytoarchitecture"],"prefix":"10.1101","volume":"11","author":[{"given":"Kerstin","family":"Andr\u00e4","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hans","family":"Lassmann","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Reginald","family":"Bittner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sigrid","family":"Shorny","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Reinhard","family":"F\u00e4ssler","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Friedrich","family":"Propst","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gerhard","family":"Wiche","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"246","published-online":{"date-parts":[[1997,12,1]]},"reference":[{"key":"2021111418494651000_11.23.3143.1","doi-asserted-by":"publisher","DOI":"10.1007\/BF02072073"},{"key":"2021111418494651000_11.23.3143.2","doi-asserted-by":"publisher","DOI":"10.1006\/dbio.1996.0346"},{"key":"2021111418494651000_11.23.3143.3","doi-asserted-by":"publisher","DOI":"10.1101\/gad.8.21.2574"},{"key":"2021111418494651000_11.23.3143.4","doi-asserted-by":"publisher","DOI":"10.1172\/JCI119028"},{"key":"2021111418494651000_11.23.3143.5","doi-asserted-by":"publisher","DOI":"10.1016\/0003-2697(87)90021-2"},{"key":"2021111418494651000_11.23.3143.6","doi-asserted-by":"publisher","DOI":"10.1083\/jcb.134.2.559"},{"key":"2021111418494651000_11.23.3143.7","doi-asserted-by":"crossref","first-page":"1307","DOI":"10.1242\/jcs.110.11.1307","article-title":"Polarization dependent association of plectin with desmoplakin and the lateral submembrane skeleton in MDCK cells.","volume":"110","author":"Eger","year":"1997","journal-title":"J. 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