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Increased Susceptibility to Hypoxic Pulmonary Hypertension in Bmpr2 Mutant Mice is Associated with Endothelial Dysfunction in the Pulmonary Vasculature Publique Deposited

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MLA citation style

de Caestecker, M, et al. Increased Susceptibility to Hypoxic Pulmonary Hypertension In Bmpr2 Mutant Mice Is Associated with Endothelial Dysfunction In the Pulmonary Vasculature. . 1120. https://mushare.marian.edu/concern/generic_works/c3de3fdb-f51d-4fe0-ab20-0507d7e08b36?locale=fr

APA citation style

de Caestecker, M, Frank, D.B, Lowery Jonathan W, Reese, J, Anderson, L, & Brink, M. (1120). Increased Susceptibility to Hypoxic Pulmonary Hypertension in Bmpr2 Mutant Mice is Associated with Endothelial Dysfunction in the Pulmonary Vasculature. https://mushare.marian.edu/concern/generic_works/c3de3fdb-f51d-4fe0-ab20-0507d7e08b36?locale=fr

Chicago citation style

de Caestecker, M., Frank, D.B., Lowery Jonathan W., Reese, J., Anderson, L., and Brink, M.. Increased Susceptibility to Hypoxic Pulmonary Hypertension In Bmpr2 Mutant Mice Is Associated with Endothelial Dysfunction In the Pulmonary Vasculature. 1120. https://mushare.marian.edu/concern/generic_works/c3de3fdb-f51d-4fe0-ab20-0507d7e08b36?locale=fr

Note: These citations are programmatically generated and may be incomplete.

Patients with familial pulmonary arterial hypertension inherit heterozygous mutations of the type 2 bone morphogenetic protein (BMP) receptor BMPR2. To explore the cellular mechanisms of this disease, we evaluated the pulmonary vascular responses to chronic hypoxia in mice carrying heterozygous hypomorphic Bmpr2 mutations (Bmpr2 delta Ex2/+). These mice develop more severe pulmonary hypertension after prolonged exposure to hypoxia without an associated increase in pulmonary vascular remodeling or proliferation compared with wild-type mice. This is associated with defective endothelial-dependent vasodilatation and enhanced vasoconstriction in isolated intrapulmonary artery preparations. In addition, there is a selective decrease in hypoxia-induced, BMP-dependent, endothelial nitric oxide synthase expression and Smad signaling in the intact lungs and in cultured pulmonary microvascular endothelial cells from Bmpr2 delta Ex2/+ mutant mice. These findings indicate that the pulmonary endothelium is a target of abnormal BMP signaling in Bmpr2 delta Ex2/+ mutant mice and suggest that endothelial dysfunction contributes to their increased susceptibility to hypoxic pulmonary hypertension.

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  • com_fp_22
  • American Journal of Physiology. Lung, Cellular and Molecular Physiology
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