Human umbilical cord mesenchymal stromal cell-derived exosomes alleviate hypoxia-induced pulmonary arterial hypertension in mice via macrophages

Author:

Liu Hong1234,Zhang Qingqing12345,Liu Chuanchuan5,Zhang Yuwei6,Wang Yuxiang1234,Huang Pan1234,Ma Lan1234,Ge Rili1234ORCID

Affiliation:

1. Research Centre for High Altitude Medicine

2. Key Laboratory of the Ministry of High Altitude Medicine

3. Key Laboratory of Applied Fundamentals of High Altitude Medicine , (Qinghai-Utah Joint Key Laboratory of Plateau Medicine)

4. Laboratory for High Altitude Medicine of Qinghai Province

5. Affiliated Hospital of Qinghai University , Xining, QingHai

6. Department of Public Health of Qinghai University

Abstract

Abstract Pulmonary hypertension (PH) is an intractable, severe, and progressive cardiopulmonary disease. Recent findings suggest that human umbilical cord mesenchymal stromal cells (HUCMSCs) and HUCMSC-derived exosomes (HUCMSC-Exos) possess potential therapeutic value for PH. However, whether they have beneficial effects on hypoxic pulmonary hypertension (HPH) is unclear. Exos are released into the extracellular environment by the fusion of intracellular multivesicular bodies with the cell membrane, and they play an important role in cellular communication. Exos ameliorate immune inflammation levels, alter macrophage phenotypes, regulate mitochondrial metabolic function, and inhibit pulmonary vascular remodelling, thereby improving PH. Macrophages are important sources of cytokines and other transmitters and can promote the release of cytokines, vasoactive molecules, and reactive oxygen species, all of which are associated with pulmonary vascular remodelling. Therefore, the aim of this study was to investigate whether HUCMSC-Exos could improve the lung inflammatory microenvironment and inhibit pulmonary vascular remodelling by targeting macrophages and identify the underlying mechanisms. The results showed that HUCMSC-Exos promoted M2 macrophage polarisation, decreased pro-inflammatory factors, increased IL-10 levels, and inhibited IL-33/ST2 axis expression, thereby inhibiting hypoxia-induced proliferation of pulmonary artery smooth muscle cells and ameliorating HPH.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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