Fibroblast Yap/Taz Signaling in Extracellular Matrix Homeostasis and Tissue Fibrosis

Author:

Chu Cong-Qiu12ORCID,Quan Taihao3ORCID

Affiliation:

1. Division of Arthritis and Rheumatic Diseases, Oregon Health & Science University, Portland, OR 97239, USA

2. Rheumatology Section, VA Portland Health Care System, Portland, OR 97239, USA

3. Department of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109, USA

Abstract

Tissue fibrosis represents a complex pathological condition characterized by the excessive accumulation of collagenous extracellular matrix (ECM) components, resulting in impaired organ function. Fibroblasts are central to the fibrotic process and crucially involved in producing and depositing collagen-rich ECM. Apart from their primary function in ECM synthesis, fibroblasts engage in diverse activities such as inflammation and shaping the tissue microenvironment, which significantly influence cellular and tissue functions. This review explores the role of Yes-associated protein (Yap) and Transcriptional co-activator with PDZ-binding motif (Taz) in fibroblast signaling and their impact on tissue fibrosis. Gaining a comprehensive understanding of the intricate molecular mechanisms of Yap/Taz signaling in fibroblasts may reveal novel therapeutic targets for fibrotic diseases.

Funder

Rheumatology Research Foundation

VA Merit Review grant

National Institute of Health

Dermatology Foundation Research grant

Publisher

MDPI AG

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