A mechanosensitive circuit of FAK, ROCK, and ERK controls biomineral growth and morphology in the sea urchin embryo

• 成果类型: Article
• 署名作者: Layous, Majed; Gildor, Tsvia; Nehrer, Tovah; Qassem, Areen; Wolfenson, Haguy; de-Leon, Smadar Ben- Tabou
• 署名单位: University of Haifa; Technion Israel Institute of Technology; Rappaport Faculty of Medicine
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-12500
• DOI: 10.1073/pnas.2408628121
• 发表日期: 2025-01-07
• 关键词: focal adhesion kinase; primary mesenchyme cells; osteogenic differentiation; signaling pathways; calcium-transport; spicule formation; activation; bone; mechanotransduction; phosphorylation

摘要

Biomineralization is the utilization of different minerals by a vast array of organisms to form hard tissues and shape them in various forms. Within this diversity, a common feature of all mineralized tissues is their high stiffness, implying that mechanosensing could be commonly used in biomineralization. Yet, the role of mechanosensing in biomineralization is far from clear. Here, we use the sea urchin larval skeletogenesis to investigate the role of substrate stiffness and focal adhesion kinase (FAK) in biomineralization. We demonstrate that substrate stiffness alters spicule morphology and growth, indicating a mechanosensitive response during skeletogenesis. We show that active FAK, F- actin, and vinculin are enriched around the spicules, indicating the formation of focal adhesion complexes and suggesting that the cells sense the mechanical properties of protein kinase (ROCK) and is crucial for skeletal growth and normal branching. FAK and ROCK activate extracellular signal- regulated kinase (ERK), which regulates skeleseems to provide essential mechanical feedback on spicule elongation to the skeletogenic mammalian osteoblast differentiation in vitro and pathological calcification in vivo. zation that was probably independently co- opted across different organisms to shape mineralized structures in metazoans.