Lin Yu, Luo Xi, Shen Xu, Fu Xiao-Lin, Lin Li-Rong, Yang Tian-Ci
Center of Clinical Laboratory School of Medicine Zhongshan Hospital Xiamen University Xiamen University Xiamen Fujian 361000 P. R. China.
Institute of Infectious Disease School of Medicine Xiamen University Xiamen Fujian 361000 P. R. China.
Small Sci. 2025 May 6;5(7):2500046. doi: 10.1002/smsc.202500046. eCollection 2025 Jul.
The membrane protein Tp0136 facilitates dissemination, and the permeability of vasculature is intricately linked to the density of the vascular endothelial barrier, which is strongly associated with the morphology of vascular endothelial cells. In this study, utilizing the approach of inoculating Tp0136 recombinant protein into the skin lesions of rabbits infected with , it was observed that the Tp0136 recombinant protein induced spheroidization of vascular endothelial cells and enlargement of intercellular junctions. By high-throughput RNA sequencing, the upregulation of the RNA-binding protein cysteine- and glycine-rich protein 1 (CSRP1) is identified, which modulated the alternative splicing of exon 19 of myosin X (MYO10), which in turn downregulated the expression of MYO10, ultimately inducing morphological spheroidization in vascular endothelial cells. Using CSRP1-specific shRNA to knock down CSRP1 or using the alternative splicing inhibitor, the spheroidized vascular endothelial cells revert to a flattened state, suggesting that Tp0136 regulates the alternative splicing of MYO10 through CSRP1, leading to a downregulation of MYO10, followed by the spheroidization of vascular endothelial cells and an enlargement of intercellular junctions. These findings contribute to elucidating a mechanism underlying the dissemination of .
膜蛋白Tp0136促进传播,脉管系统的通透性与血管内皮屏障的密度密切相关,而血管内皮屏障的密度与血管内皮细胞的形态密切相关。在本研究中,采用将Tp0136重组蛋白接种到感染的家兔皮肤损伤处的方法,观察到Tp0136重组蛋白诱导血管内皮细胞球形化和细胞间连接增大。通过高通量RNA测序,鉴定出富含半胱氨酸和甘氨酸的RNA结合蛋白1(CSRP1)上调,其调节肌球蛋白X(MYO10)第19外显子的可变剪接,进而下调MYO10的表达,最终诱导血管内皮细胞形态球形化。使用CSRP1特异性短发夹RNA敲低CSRP1或使用可变剪接抑制剂,球形化的血管内皮细胞恢复为扁平状态,表明Tp0136通过CSRP1调节MYO10的可变剪接,导致MYO10下调,随后血管内皮细胞球形化和细胞间连接增大。这些发现有助于阐明传播的潜在机制。