Plakophilin3 increases desmosome assembly, size and stability by increasing expression of desmocollin2

التفاصيل البيبلوغرافية
العنوان: Plakophilin3 increases desmosome assembly, size and stability by increasing expression of desmocollin2
المؤلفون: Sorab N. Dalal, Mansi S. Karkhanis, Apurva Atak, Kumarkrishna Raychaudhuri, Lalit Sehgal, Prajakta Gosavi, Kruthi Rao, Divya Reddy, Snehal Mahadik, Sanjay Gupta, Trupti Shetty, Mansa Gurjar
المصدر: Biochemical and Biophysical Research Communications. 495:768-774
بيانات النشر: Elsevier BV, 2018.
سنة النشر: 2018
مصطلحات موضوعية: 0301 basic medicine, Cell, Biophysics, chemistry.chemical_element, Calcium, Biochemistry, Cell Line, 03 medical and health sciences, 0302 clinical medicine, Protein stability, Desmosome, Transcription (biology), Cell Adhesion, medicine, Humans, Particle Size, Molecular Biology, Desmocollins, DSC2, Desmosomes, Cell Biology, Low calcium, Cell biology, 030104 developmental biology, medicine.anatomical_structure, chemistry, 030220 oncology & carcinogenesis, Desmosome assembly, Plakophilins
الوصف: Previous reports show that the desmosomal plaque protein plakophilin3 (PKP3) is essential for desmosome formation. Here, we report that PKP3 over-expression decreases calcium dependency for de novo desmosome formation and makes existing cell-cell adhesion junctions more resilient in low calcium medium due to an increase in desmocollin2 expression. PKP3 overexpression increases the stability of other desmosomal proteins independently of the increase in DSC2 levels and regulates desmosome formation and stability by a multimodal mechanism affecting transcription, protein stability and cell border localization of desmosomal proteins.
تدمد: 0006-291X
DOI: 10.1016/j.bbrc.2017.11.085
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b78dabf469bce8ee1f5f0e11a12b2ca
https://doi.org/10.1016/j.bbrc.2017.11.085
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....2b78dabf469bce8ee1f5f0e11a12b2ca
قاعدة البيانات: OpenAIRE
الوصف
تدمد:0006291X
DOI:10.1016/j.bbrc.2017.11.085