Aggrecan accumulates at sites of increased pulmonary arterial pressure in idiopathic pulmonary arterial hypertension

• Published in: Pulmonary circulation Vol. 13; no. 1; pp. e12200 - n/a
• Main Authors: Have, Oscar, Mead, Timothy J., Westöö, Christian, Peruzzi, Niccolò, Mutgan, Ayse C., Norvik, Christian, Bech, Martin, Struglics, André, Hoetzenecker, Konrad, Brunnström, Hans, Westergren‐Thorsson, Gunilla, Kwapiszewska, Grazyna, Apte, Suneel S., Tran‐Lundmark, Karin
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.01.2023; John Wiley and Sons Inc; Wiley
• Subjects: Basic Medicine; Cell and Molecular Biology; Cell- och molekylärbiologi; extracellular matrix; Medical and Health Sciences; Medicin och hälsovetenskap; Medicinska och farmaceutiska grundvetenskaper; proteoglycan; pulmonary arterial hypertension; Pulmonary arteries; Pulmonary hypertension; synchrotron imaging; vascular disease; Veins & arteries; synchrotron imaging; vascular disease; pulmonary arterial hypertension; extracellular matrix; proteoglycan
• ISSN: 2045-8940; 2045-8932; 2045-8940
• DOI: 10.1002/pul2.12200

Expansion of extracellular matrix occurs in all stages of pulmonary angiopathy associated with pulmonary arterial hypertension (PAH). In systemic arteries, dysregulation and accumulation of the large chondroitin‐sulfate proteoglycan aggrecan is associated with swelling and disruption of vessel wall homeostasis. Whether aggrecan is present in pulmonary arteries, and its potential roles in PAH, has not been thoroughly investigated. Here, lung tissue from 11 patients with idiopathic PAH was imaged using synchrotron radiation phase‐contrast microcomputed tomography (TOMCAT beamline, Swiss Light Source). Immunohistochemistry for aggrecan core protein in subsequently sectioned lung tissue demonstrated accumulation in PAH compared with failed donor lung controls. RNAscope in situ hybridization indicated ACAN expression in vascular endothelium and smooth muscle cells. Based on qualitative histological analysis, aggrecan localizes to cellular, rather than fibrotic or collagenous, lesions. Interestingly, ADAMTS15, a potential aggrecanase, was upregulated in pulmonary arteries in PAH. Aligning traditional histological analysis with three‐dimensional renderings of pulmonary arteries from synchrotron imaging identified aggrecan in lumen‐reducing lesions containing loose, cell‐rich connective tissue, at sites of intrapulmonary bronchopulmonary shunting, and at sites of presumed elevated pulmonary blood pressure. Our findings suggest that ACAN expression may be an early response to injury in pulmonary angiopathy and supports recent work showing that dysregulation of aggrecan turnover is a hallmark of arterial adaptations to altered hemodynamics. Whether cause or effect, aggrecan and aggrecanase regulation in PAH are potential therapeutic targets.