Hypoxia-induced mitogenic factor (HIMF/FIZZ1/RELM alpha) recruits bone marrow-derived cells to the murine pulmonary vasculature

التفاصيل البيبلوغرافية
العنوان: Hypoxia-induced mitogenic factor (HIMF/FIZZ1/RELM alpha) recruits bone marrow-derived cells to the murine pulmonary vasculature
المؤلفون: Daniel J. Angelini, Qingning Su, Irina A. Kolosova, Saul J. Sharkis, Roger A. Johns, Kazuyo Yamaji-Kegan, John Skinner, Chunling Fan, Michael I. Collector
المصدر: PLoS ONE
PLoS ONE, Vol 5, Iss 6, p e11251 (2010)
سنة النشر: 2010
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Blotting, Western, Genetic Vectors, CD34, lcsh:Medicine, Inflammation, Bone Marrow Cells, Mice, Transgenic, 030204 cardiovascular system & hematology, Biology, 03 medical and health sciences, Mice, 0302 clinical medicine, medicine, Animals, Cardiovascular Disorders/Vascular Biology, Progenitor cell, lcsh:Science, Hypoxia, Lung, 030304 developmental biology, Bone Marrow Transplantation, 0303 health sciences, Cardiovascular Disorders/Pulmonary Vascular Diseases, Multidisciplinary, Chemotaxis, lcsh:R, Mesenchymal stem cell, Cell migration, Cell Biology, Dependovirus, medicine.disease, Pulmonary hypertension, Immunohistochemistry, 3. Good health, Mice, Inbred C57BL, medicine.anatomical_structure, Microscopy, Fluorescence, Cancer research, Blood Vessels, Intercellular Signaling Peptides and Proteins, lcsh:Q, Female, Bone marrow, medicine.symptom, Stem cell, Research Article
الوصف: Background Pulmonary hypertension (PH) is a disease of multiple etiologies with several common pathological features, including inflammation and pulmonary vascular remodeling. Recent evidence has suggested a potential role for the recruitment of bone marrow-derived (BMD) progenitor cells to this remodeling process. We recently demonstrated that hypoxia-induced mitogenic factor (HIMF/FIZZ1/RELM alpha) is chemotactic to murine bone marrow cells in vitro and involved in pulmonary vascular remodeling in vivo. Methodology/principal findings We used a mouse bone marrow transplant model in which lethally irradiated mice were rescued with bone marrow transplanted from green fluorescent protein (GFP)(+) transgenic mice to determine the role of HIMF in recruiting BMD cells to the lung vasculature during PH development. Exposure to chronic hypoxia and pulmonary gene transfer of HIMF were used to induce PH. Both models resulted in markedly increased numbers of BMD cells in and around the pulmonary vasculature; in several neomuscularized small (approximately 20 microm) capillary-like vessels, an entirely new medial wall was made up of these cells. We found these GFP(+) BMD cells to be positive for stem cell antigen-1 and c-kit, but negative for CD31 and CD34. Several of the GFP(+) cells that localized to the pulmonary vasculature were alpha-smooth muscle actin(+) and localized to the media layer of the vessels. This finding suggests that these cells are of mesenchymal origin and differentiate toward myofibroblast and vascular smooth muscle. Structural location in the media of small vessels suggests a functional role in the lung vasculature. To examine a potential mechanism for HIMF-dependent recruitment of mesenchymal stem cells to the pulmonary vasculature, we performed a cell migration assay using cultured human mesenchymal stem cells (HMSCs). The addition of recombinant HIMF induced migration of HMSCs in a phosphoinosotide-3-kinase-dependent manner. Conclusions/significance These results demonstrate HIMF-dependent recruitment of BMD mesenchymal-like cells to the remodeling pulmonary vasculature.
تدمد: 1932-6203
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c14ba661cd93d94b3980edc557207f2
https://pubmed.ncbi.nlm.nih.gov/20582166
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....9c14ba661cd93d94b3980edc557207f2
قاعدة البيانات: OpenAIRE