Research: A pneumonectomy model to study flow-induced pulmonary hypertension and compensatory lung growth

Cell Rep Methods

. 2023 Oct 4:100613.

 doi: 10.1016/j.crmeth.2023.100613. Online ahead of print. https://pubmed.ncbi.nlm.nih.gov/37827157/

A pneumonectomy model to study flow-induced pulmonary hypertension and compensatory lung growth

Savas T Tsikis 1Timothy Klouda 2Thomas I Hirsch 1Scott C Fligor 1Tiffany Liu 2Yunhye Kim 2Amy Pan 1Mikayla Quigley 1Paul D Mitchell 3Mark Puder 4Ke Yuan 5

Affiliations expand

Abstract

In newborns, developmental disorders such as congenital diaphragmatic hernia (CDH) and specific types of congenital heart disease (CHD) can lead to defective alveolarization, pulmonary hypoplasia, and pulmonary arterial hypertension (PAH). Therapeutic options for these patients are limited, emphasizing the need for new animal models representative of disease conditions. In most adult mammals, compensatory lung growth (CLG) occurs after pneumonectomy; however, the underlying relationship between CLG and flow-induced pulmonary hypertension (PH) is not fully understood. We propose a murine model that involves the simultaneous removal of the left lung and right caval lobe (extended pneumonectomy), which results in reduced CLG and exacerbated reproducible PH. Extended pneumonectomy in mice is a promising animal model to study the cellular response and molecular mechanisms contributing to flow-induced PH, with the potential to identify new treatments for patients with CDH or PAH-CHD.

Keywords: CP: Biotechnology; animal models; compensatory lung growth; pneumonectomy; pulmonary hypertension; pulmonary hypoplasia.

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