Canon Stroke and Vascular Research Center, University at Buffalo, Buffalo, NY, USA.
Department of Pathology and Anatomical Sciences, University at Buffalo, 955 Main Street, Room 4102, Buffalo, NY, 14203, USA.
Sci Rep. 2021 Aug 9;11(1):16142. doi: 10.1038/s41598-021-95403-x.
Changes in blood flow can induce arterial remodeling. Intimal cells sense flow and send signals to the media to initiate remodeling. However, the nature of such intima-media signaling is not fully understood. To identify potential signals, New Zealand white rabbits underwent bilateral carotid ligation to increase flow in the basilar artery or sham surgery (n = 2 ligated, n = 2 sham). Flow was measured by transcranial Doppler ultrasonography, vessel geometry was determined by 3D angiography, and hemodynamics were quantified by computational fluid dynamics. 24 h post-surgery, the basilar artery and terminus were embedded for sectioning. Intima and media were separately microdissected from the sections, and whole transcriptomes were obtained by RNA-seq. Correlation analysis of expression across all possible intima-media gene pairs revealed potential remodeling signals. Carotid ligation increased flow in the basilar artery and terminus and caused differential expression of 194 intimal genes and 529 medial genes. 29,777 intima-media gene pairs exhibited correlated expression. 18 intimal genes had > 200 medial correlates and coded for extracellular products. Gene ontology of the medial correlates showed enrichment of organonitrogen metabolism, leukocyte activation/immune response, and secretion/exocytosis processes. This demonstrates correlative expression analysis of intimal and medial genes can reveal novel signals that may regulate flow-induced arterial remodeling.
血流变化可诱导动脉重塑。内膜细胞感知血流并向中膜发送信号,启动重塑过程。然而,这种内膜-中膜信号传递的性质尚不完全清楚。为了鉴定潜在的信号分子,我们对新西兰白兔进行双侧颈动脉结扎,以增加基底动脉的血流量或假手术(结扎 2 只,假手术 2 只)。通过经颅多普勒超声测量血流,通过 3D 血管造影术确定血管几何形状,并通过计算流体动力学量化血流动力学。手术后 24 小时,将基底动脉和末端包埋进行切片。从切片中分别分离内膜和中膜,并通过 RNA-seq 获得全转录组。对所有可能的内膜-中膜基因对的表达进行相关分析,揭示了潜在的重塑信号。颈动脉结扎增加了基底动脉和末端的血流量,并导致 194 个内膜基因和 529 个中膜基因的差异表达。29777 个内膜-中膜基因对表现出相关表达。18 个内膜基因有超过 200 个中膜相关基因,编码细胞外产物。中膜相关基因的基因本体论显示出器官氮代谢、白细胞激活/免疫反应和分泌/胞吐过程的富集。这表明内膜和中膜基因的相关表达分析可以揭示可能调节血流诱导的动脉重塑的新信号。