Functions of actin-binding proteins in cilia structure remodeling and signaling

被引:2
|
作者
Wang, Siqi [1 ,2 ]
Wang, Xin [3 ]
Pan, Congbin [1 ,2 ]
Liu, Ying [4 ]
Lei, Min [1 ]
Guo, Xiying [1 ]
Chen, Qingjie [1 ]
Yang, Xiaosong [1 ]
Ouyang, Changhan [2 ]
Ren, Zhanhong [1 ,5 ]
机构
[1] Hubei Univ Sci & Technol, Med Res Inst, Xianning Med Coll, Hubei Key Lab Diabet & Angiopathy, Xianning, Peoples R China
[2] Hubei Univ Sci & Technol, Xianning Med Coll, Sch Pharm, Xianning, Peoples R China
[3] Hubei Univ Sci & Technol, Sch Math & Stat, Xianning, Peoples R China
[4] Shandong Normal Univ, Coll Life Sci, Shandong Prov Key Lab Anim Resistance Biol, Jinan, Peoples R China
[5] Hubei Univ Sci & Technol, Med Res Inst, Xianning Med Coll, Hubei Key Lab Diabet & Angiopathy, Xianning 437100, Peoples R China
关键词
actin cytoskeleton; cilia; ciliogenesis; signaling pathway; INTRAFLAGELLAR TRANSPORT; MYOSIN VIIA; CILIOGENESIS; LENGTH; LOCALIZATION; ENDOCYTOSIS; POLYCYSTIN; DYNAMICS; MECKELIN; GROWTH;
D O I
10.1111/boc.202300026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cilia are microtubule-based organelles found on the surfaces of many types of cells, including cardiac fibroblasts, vascular endothelial cells, human retinal pigmented epithelial-1 (RPE-1) cells, and alveolar epithelial cells. These organelles can be classified as immotile cilia, referred to as primary cilia in mammalian cells, and motile cilia. Primary cilia are cellular sensors that detect extracellular signals; this is a critical function associated with ciliopathies, which are characterized by the typical clinical features of developmental disorders. Cilia are extensively studied organelles of the microtubule cytoskeleton. However, the ciliary actin cytoskeleton has rarely been studied. Clear evidence has shown that highly regulated actin cytoskeleton dynamics contribute to normal ciliary function. Actin-binding proteins (ABPs) play vital roles in filamentous actin (F-actin) morphology. Here, we discuss recent progress in understanding the roles of ABPs in ciliary structural remodeling and further downstream ciliary signaling with a focus on the molecular mechanisms underlying actin cytoskeleton-related ciliopathies.
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页数:10
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