The Journal of clinical investigation, 2017-06, Vol.127 (6), p.2262-2276
2017
Details
- Autor(en) / Beteiligte
- Titel
- Disruption of lineage specification in adult pulmonary mesenchymal progenitor cells promotes microvascular dysfunction
- Ist Teil von
- The Journal of clinical investigation, 2017-06, Vol.127 (6), p.2262-2276
- Ort / Verlag
- United States: American Society for Clinical Investigation
- Erscheinungsjahr
- 2017
- Link zum Volltext
- Quelle
- Free E-Journal (出版社公開部分のみ）
- Beschreibungen/Notizen
- Pulmonary vascular disease is characterized by remodeling and loss of microvessels and is typically attributed to pathological responses in vascular endothelium or abnormal smooth muscle cell phenotypes. We have challenged this understanding by defining an adult pulmonary mesenchymal progenitor cell (MPC) that regulates both microvascular function and angiogenesis. The current understanding of adult MPCs and their roles in homeostasis versus disease has been limited by a lack of genetic markers with which to lineage label multipotent mesenchyme and trace the differentiation of these MPCs into vascular lineages. Here, we have shown that lineage-labeled lung MPCs expressing the ATP-binding cassette protein ABCG2 (ABCG2+) are pericyte progenitors that participate in microvascular homeostasis as well as adaptive angiogenesis. Activation of Wnt/β-catenin signaling, either autonomously or downstream of decreased BMP receptor signaling, enhanced ABCG2+ MPC proliferation but suppressed MPC differentiation into a functional pericyte lineage. Thus, enhanced Wnt/β-catenin signaling in ABCG2+ MPCs drives a phenotype of persistent microvascular dysfunction, abnormal angiogenesis, and subsequent exacerbation of bleomycin-induced fibrosis. ABCG2+ MPCs may, therefore, account in part for the aberrant microvessel function and remodeling that are associated with chronic lung diseases.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0021-9738eISSN: 1558-8238DOI: 10.1172/jci88629Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5451236
- Format
- –
- Schlagworte
- Adenosine triphosphatase, Angiogenesis, Animals, ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism, Biomedical research, Bleomycin, Bone Morphogenetic Protein Receptors, Type II - metabolism, Bone morphogenetic proteins, Cell Differentiation, Cell Lineage, Cells, Cultured, Chronic obstructive pulmonary disease, Endothelium, Fibrosis, Functional anatomy, Genetic markers, Homeostasis, Humans, Hypoxia, Lung - blood supply, Lung diseases, Medical prognosis, Mesenchymal Stem Cells - physiology, Mesenchyme, Mice, Transgenic, Microvasculature, Microvessels - pathology, Microvessels - physiopathology, Mutation, Neovascularization, Pathologic - metabolism, Pericytes - physiology, Progenitor cells, Protein Stability, Proteins, Pulmonary arteries, Pulmonary Fibrosis - metabolism, Pulmonary Fibrosis - pathology, Pulmonary hypertension, Roles, Smooth muscle, Stem cells, Vasoconstriction, Wnt protein, Wnt Signaling Pathway, β-Catenin