IRE1α pathway: A potential bone metabolism mediator

Author:

Yu Chengbo123,Zhang Zhixiang123,Xiao Li123,Ai Mi123,Qing Ying123,Zhang Zhixing123,Xu Lianyi123,Yu Ollie Yiru4,Cao Yingguang123,Liu Yong5,Song Ke123ORCID

Affiliation:

1. Department of Stomatology, Tongji Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

2. Department of Prosthodontics and Implantology, School of Stomatology, Tongji Medical College Huazhong University of Science and Technology Wuhan China

3. Hubei Province Key Laboratory of Oral and Maxillofacial Development and Regeneration Wuhan China

4. Faculty of Dentistry The University of Hong Kong Hong Kong SAR China

5. Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Frontier Science Center for Immunology and Metabolism, and the Institute for Advanced Studies Wuhan University Wuhan Hubei China

Abstract

AbstractOsteoblasts and osteoclasts collaborate in bone metabolism, facilitating bone development, maintaining normal bone density and strength, and aiding in the repair of pathological damage. Endoplasmic reticulum stress (ERS) can disrupt the intracellular equilibrium between osteoclast and osteoblast, resulting in dysfunctional bone metabolism. The inositol‐requiring enzyme‐1α (IRE1α) pathway—the most conservative unfolded protein response pathway activated by ERS—is crucial in regulating cell metabolism. This involvement encompasses functions such as inflammation, autophagy, and apoptosis. Many studies have highlighted the potential roles of the IRE1α pathway in osteoblasts, chondrocytes, and osteoclasts and its implication in certain bone‐related diseases. These findings suggest that it may serve as a mediator for bone metabolism. However, relevant reviews on the role of the IRE1α pathway in bone metabolism remain unavailable. Therefore, this review aims to explore recent research that elucidated the intricate roles of the IRE1α pathway in bone metabolism, specifically in osteogenesis, chondrogenesis, osteoclastogenesis, and osteo‐immunology. The findings may provide novel insights into regulating bone metabolism and treating bone‐related diseases.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Wiley

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