Mice expressing BMPR2R899X transgene in smooth muscle develop pulmonary vascular lesions.

West J, Harral J, Lane K, Deng Y, Ickes B, Crona D, Albu S, Stewart D, Fagan K
Am J Physiol Lung Cell Mol Physiol. 2008 295 (5): L744-55

PMID: 18723761 · PMCID: PMC2584890 · DOI:10.1152/ajplung.90255.2008

Familial pulmonary arterial hypertension (PAH) is associated with mutations in bone morphogenetic protein type II receptor (BMPR2). Many of these mutations occur in the BMPR2 tail domain, leaving the SMAD functions intact. To determine the in vivo consequences of BMPR2 tail domain mutation, we created a smooth muscle-specific doxycycline-inducible BMPR2 mutation with an arginine to termination mutation at amino acid 899. When these SM22-rtTA x TetO(7)-BMPR2(R899X) mice had transgene induced for 9 wk, starting at 4 wk of age, they universally developed pulmonary vascular pruning as assessed by fluorescent microangiography. Approximately one-third of the time, the induced animals developed elevated right ventricular systolic pressures (RVSP), associated with extensive pruning, muscularization of small pulmonary vessels, and development of large structural pulmonary vascular changes. These lesions included large numbers of macrophages and T cells in their adventitial compartment as well as CD133-positive cells in the lumen. Small vessels filled with CD45-positive and sometimes CD3-positive cells were a common feature in all SM22-rtTA x TetO(7)-BMPR2(R899X) mice. Gene array experiments show changes in stress response, muscle organization and function, proliferation, and apoptosis and developmental pathways before RVSP increases. Our results show that the primary phenotypic result of BMPR2 tail domain mutation in smooth muscle is pulmonary vascular pruning leading to elevated RVSP, associated with early dysregulation in multiple pathways with clear relevance to PAH. This model should be useful to the research community in examining early molecular and physical events in the development of PAH and as a platform to validate potential treatments.

MeSH Terms (26)

AC133 Antigen Animals Antigens, CD Blood Pressure Blood Vessels Bone Morphogenetic Protein Receptors, Type II Cell Cycle Endothelium Gene Expression Regulation Glycoproteins Heart Ventricles Hypertension, Pulmonary Leukocyte Common Antigens Macrophages Mice Mitogen-Activated Protein Kinase 1 Muscle, Smooth Mutant Proteins Neovascularization, Pathologic p38 Mitogen-Activated Protein Kinases Peptides Phosphorylation Smad Proteins Systole T-Lymphocytes Transgenes

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