The keratin-desmosome scaffold of internal epithelia in health and disease - The plot is thickening

Diana M Toivola, Lauri Polari, Tobias Schwerd, Nicolas Schlegel, Pavel Strnad

Research output: Contribution to journalReview Article or Literature Reviewpeer-review

7 Citations (Scopus)
141 Downloads (Pure)

Abstract

Keratin (K) intermediate filaments are attached to desmosomes and constitute the orchestrators of epithelial cell and tissue architecture. While their relevance in the epidermis is well recognized, our review focuses on their emerging importance in internal epithelia. The significance of keratin-desmosome scaffolds (KDSs) in the intestine is highlighted by transgenic mouse models and individuals with inflammatory bowel disease who display profound KDS alterations. In lung, high K8 expression defines a transitional cell subset during regeneration, and K8 variants are associated with idiopathic pulmonary fibrosis. Inherited variants in desmosomal proteins are overrepresented in idiopathic lung fibrosis, and familiar eosinophilic esophagitis. K18 serum fragments are established hepatocellular injury markers that correlate with the extent of histological inflammation. K17 expression is modified in multiple tumors, and K17 levels might be of prognostic relevance. These data should spur further studies on biological roles of these versatile tissue protectors and efforts on their therapeutic targeting.

Original languageEnglish
Article number102282
Number of pages8
JournalCurrent Opinion in Cell Biology
Volume86
DOIs
Publication statusPublished - Feb 2024
MoE publication typeA2 Review article in a scientific journal

Funding

We thank everyone who contributed to the field and apologize for the references that had to be left out due to space restrictions. DMT is supported by the Academy of Finland (315139 and 332582), including the InFLAMES Flagship (337531 and 357911), Novo Nordisk Foundation (NNF20OC0063889), Åbo Akademi University Foundation /Åbo Akademi University Center of Excellence in Mechanostasis and Medicinska Understödsföreningen Liv och Hälsa Foundation. PS is supported by the Deutsche Forschungsgemeinschaft ( DFG ) grants SFB 1382 (ID 403224013) and STR 1095/6-1. NS is supported by DFG grants SCHL1962/8-1 and SCHL1962/5-2. TS is supported by DFG through the Collaborative Research Center 1371 (project number 395357507) and by the Munich Medical & Clinician Scientist Program (MCSP).

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