دورية أكاديمية

Cellular Transdifferentiation: A Crucial Mechanism of Fibrosis in Systemic Sclerosis.

التفاصيل البيبلوغرافية
العنوان: Cellular Transdifferentiation: A Crucial Mechanism of Fibrosis in Systemic Sclerosis.
المؤلفون: Jimenez SA; Department of Dermatology and Cutaneous Biology, Jefferson Institute of Molecular Medicine and Scleroderma Center, Thomas Jefferson University, Philadelphia 19107, USA., Piera-Velazquez S; Department of Dermatology and Cutaneous Biology, Jefferson Institute of Molecular Medicine and Scleroderma Center, Thomas Jefferson University, Philadelphia 19107, USA.
المصدر: Current rheumatology reviews [Curr Rheumatol Rev] 2024; Vol. 20 (4), pp. 388-404.
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Bentham Science Publishers Country of Publication: United Arab Emirates NLM ID: 101261938 Publication Model: Print Cited Medium: Internet ISSN: 1875-6360 (Electronic) Linking ISSN: 15733971 NLM ISO Abbreviation: Curr Rheumatol Rev Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Saif Zone, Sharjah, U.A.E. ; San Francisco, CA : Bentham Science Publishers, 2005-
مواضيع طبية MeSH: Scleroderma, Systemic*/pathology , Cell Transdifferentiation* , Fibrosis*, Humans ; Myofibroblasts/pathology
مستخلص: Systemic Sclerosis (SSc) is a systemic autoimmune disease of unknown etiology with a highly complex pathogenesis that despite extensive investigation is not completely understood. The clinical and pathologic manifestations of the disease result from three distinct processes: 1) Severe and frequently progressive tissue fibrosis causing exaggerated and deleterious accumulation of interstitial collagens and other extracellular matrix molecules in the skin and various internal organs; 2) extensive fibroproliferative vascular lesions affecting small arteries and arterioles causing tissue ischemic alterations; and 3) cellular and humoral immunity abnormalities with the production of numerous autoantibodies, some with very high specificity for SSc. The fibrotic process in SSc is one of the main causes of disability and high mortality of the disease. Owing to its essentially universal presence and the severity of its clinical effects, the mechanisms involved in the development and progression of tissue fibrosis have been extensively investigated, however, despite intensive investigation, the precise molecular mechanisms have not been fully elucidated. Several recent studies have suggested that cellular transdifferentiation resulting in the phenotypic conversion of various cell types into activated myofibroblasts may be one important mechanism. Here, we review the potential role that cellular transdifferentiation may play in the development of severe and often progressive tissue fibrosis in SSc.
(Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)
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معلومات مُعتمدة: Award Number AM19606 United States NH NIH HHS
فهرسة مساهمة: Keywords: Systemic sclerosis; cellular transdifferentiation; cytokines.; growth factors; myofibroblasts; scleroderma
تواريخ الأحداث: Date Created: 20231103 Date Completed: 20240606 Latest Revision: 20240617
رمز التحديث: 20240617
DOI: 10.2174/0115733971261932231025045400
PMID: 37921216
قاعدة البيانات: MEDLINE
الوصف
تدمد:1875-6360
DOI:10.2174/0115733971261932231025045400