Smooth muscle Cxcl12 contributions to vascular remodeling in flow and hypoxia-induced pulmonary hypertension.

Abstract

Patients with congenital heart disease (CHD) causing significant left-to-right shunting of blood are at risk of developing pulmonary arterial hypertension (PAH). However, the underlying mechanism by which pulmonary overcirculation and shear stress drive vascular remodeling remains poorly understood. Our study established a "two-hit" murine model of severe pulmonary hypertension (PH) by combining left pneumonectomy (LP) and chronic hypoxia (LP/Hx). Using transgenic reporter lines, immunofluorescence (IF) staining, and advanced microscopy, we conducted cell-lineage tracing for vascular cells, including smooth muscle cells (SMCs), endothelial cells (ECs), and pericytes. Our findings reveal that SMCs are key contributors to the distal arteriolar remodeling following LP and LP/Hx. PCR analysis of SMCs isolated from LP/Hx animals demonstrated upregulation of markers associated with contractility, proliferation, and Cxcl12 expression. Consistently, CXCL12 was found to be overexpressed in the SMC layer of pulmonary vessels from patients with PAH-CHD. Lastly, in vitro experiments with healthy human pulmonary artery SMCs showed that laminar shear stress induces CXCL12 upregulation. These findings provide novel insights into the role of SMCs in flow-induced vascular remodeling and their mechanosensitive response to shear stress. This murine model of severe PH is a valuable tool for future research and developing targeted therapeutics for patients with PAH.