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| 1 | Circulating Blood Endothelial Nitric Oxide Synthase Contributes to the Regulation of Systemic Blood Pressure and Nitrite Homeostasis显示文摘 | Katherine C. Wood Miriam M. Cortese-Krott Jason C. Kovacic Audrey Noguchi Virginia B. Liu Xunde Wang Nalini Raghavachari Manfred Boehm Gregory J. Kato Malte Kelm Mark T. Gladwin | 2013 | Arteriosclerosis, Thrombosis, and Vascular Biology2013，，： | 1 |
| 2 | Regulation of Smooth Muscle Cell Proliferation by β-Catenin/T-Cell Factor Signaling Involves Modulation of Cyclin D1 and p21 Expression显示文摘 | Helen Quasnichka Sadie C. Slater Cressida A. Beeching Manfred Boehm Graciela B. Sala-Newby Sarah J. George | 2006 | Circulation Research2006，，： | 1 |
| 3 | Angiotensin converting enzyme 2 - A New Cardiac REGULATOR显示文摘 | Manfred Boehm MD Eliizabeth G Nabel MD | 2002 | N Engl J Med2002，，1： | 1 |
| 4 | Circulating Blood Endothelial Nitric Oxide Synthase Contributes to the Regulation of Systemic Blood Pressure and Nitrite Homeostasis显示文摘 | Katherine C. Wood Miriam M. Cortese-Krott Jason C. Kovacic Audrey Noguchi Virginia B. Liu Xunde Wang Nalini Raghavachari Manfred Boehm Gregory J. Kato Malte Kelm Mark T. Gladwin | 2013 | Arteriosclerosis Thrombosis and Vascular Biology2013，，8： | 1 |
| 5 | VEGFR1/CXCR4-positive progenitor cells modulate local inflammation and augment tissue perfusion by a SDF-1-dependent mechanism显示文摘Recruitment and retention of circulating progenitor cells at the site of injured or ischemic tissues facilitates adult neovascularization.We hypothesized that cell therapy could modulate local neo-vascularization through the vascular endothelial growth factor(VEGF)/stromal cellderived factor-1(SDF-1)axis and by paracrine effects on local endothelial cells.We isolated from rat bone marrow a subset of multipotent adult progenitor cell-derived progenitor cells(MDPC).In vitro,MDPCs secreted multiple cytokines related to inflammation and angiogenesis,including monocyte chemotactic protein-1,SDF-1,basic fibroblast growth factor,and VEGF,and expressed the chemokine receptors CXCR4 and VEGFR1.To investigate in vivo properties,we transplanted MDPCs into the ischemic hind limbs of rats.Elevated levels of the chemokine SDF-1 and colocalization of CD11b^+cells marked the initial phase of tissue remodeling after cell transplantation.Prolonged engraftment was observed in the adventitial-medial border region of arterioles of ischemic muscles.However,engrafted cells did not differentiate into endothelial or smooth muscle cells.Limb perfusion normalized 4 weeks after cell injection.Inhibition of SDF-1 reduced the engraftment of transplanted cells and decreased endothelial cell proliferation.These findings suggest a two-stage model whereby transplanted MDPCs modulate wound repair through recruitment of inflammatory cells to ischemic tissue.This is an important potential mechanism for cell transplantation,in addition to the direct modulation of local vascular cells through paracrine mechanisms. | Andrew Wragg Jason A.Mellad Leilani E.Beltran Mikhail Konoplyannikov Hong San Sherry Boozer Robert J.Deans Anthony Mathur Robert J.Lederman Jason C.Kovacic Manfred Boehm | 2016 | 世界最新医学信息文摘2016，16，2： | 0 |
| 6 | VEGFR1/CXCR4-positive progenitor cells modulate local inflammation and augment tissue perfusion by a SDF-1-dependent mechanism显示文摘Recruitment and retention of circulating progenitor cells at the site of injured or ischemic tissues facilitates adult neovascularization. We hypothesized that cell therapy could modulate local neo-vascularization through the vascular endothelial growth factor(VEGF)/stromal cellderived factor-1(SDF-1) axis and by paracrine effects on local endothelial cells. We isolated from rat bone marrow a subset of multipotent adult progenitor cell-derived progenitor cells(MDPC). In vitro, MDPCs secreted multiple cytokines related to inflammation and angiogenesis, including monocyte chemotactic protein-1, SDF-1, basic fibroblast growth factor, and VEGF, and expressed the chemokine receptors CXCR4 and VEGFR1. To investigate in vivo properties, we transplanted MDPCs into the ischemic hind limbs of rats. Elevated levels of the chemokine SDF-1 and colocalization of cd11b+ cells marked the initial phase of tissue remodeling after cell transplantation. Prolonged engraftment was observed in the adventitial–medial border region of arterioles of ischemic muscles. However, engrafted cells did not differentiate into endothelial or smooth muscle cells. Limb perfusion normalized 4 weeks after cell injection. Inhibition of SDF-1 reduced the engraftment of transplanted cells and decreased endothelial cell proliferation. These findings suggest a two-stage model whereby transplanted MDPCs modulate wound repair through recruitment of inflammatory cells to ischemic tissue. This is an important potential mechanism for cell transplantation, in addition to the direct modulation of local vascular cells through paracrine mechanisms. | Andrew Wragg Jason A.Mellad Leilani E.Beltran Mikhail Konoplyannikov Hong San Sherry Boozer Robert J.Deans Anthony Mathur Robert J.Lederman Jason C.Kovacic Manfred Boehm | 2015 | 世界最新医学信息文摘2015，15，99： | 0 |
| 7 | VEGFR1/CXCR4-positive progenitor cells modulate local inflammation and augment tissue perfusion by a SDF-1-dependent mechanism显示文摘Recruitment and retention of circulating progenitor cells at the site of injured or ischemic tissues facilitates adult neovascularization. We hypothesized that cell therapy could modulate local neo-vascularization through the vascular endothelial growth factor(VEGF)/stromal cellderived factor-1(SDF-1) axis and by paracrine effects on local endothelial cells. We isolated from rat bone marrow a subset of multipotent adult progenitor cell-derived progenitor cells(MDPC). In vitro, MDPCs secreted multiple cytokines related to inflammation and angiogenesis, including monocyte chemotactic protein-1, SDF-1, basic fibroblast growth factor, and VEGF, and expressed the chemokine receptors CXCR4 and VEGFR1. To investigate in vivo properties, we transplanted MDPCs into the ischemic hind limbs of rats. Elevated levels of the chemokine SDF-1 and colocalization of cd11b+ cells marked the initial phase of tissue remodeling after cell transplantation. Prolonged engraftment was observed in the adventitial–medial border region of arterioles of ischemic muscles. However, engrafted cells did not differentiate into endothelial or smooth muscle cells. Limb perfusion normalized 4 weeks after cell injection. Inhibition of SDF-1 reduced the engraftment of transplanted cells and decreased endothelial cell proliferation. These findings suggest a two-stage model whereby transplanted MDPCs modulate wound repair through recruitment of inflammatory cells to ischemic tissue. This is an important potential mechanism for cell transplantation, in addition to the direct modulation of local vascular cells through paracrine mechanisms. | Andrew Wragg Jason A.Mellad Leilani E.Beltran Mikhail Konoplyannikov Hong San Sherry Boozer Robert J.Deans Anthony Mathur Robert J.Lederman Jason C.Kovacic Manfred Boehm | 2015 | 世界最新医学信息文摘2015，15，A0： | 0 |
| 8 | VEGFR1/CXCR4-positive progenitor cells modulate local inflammation and augment tissue perfusion by a SDF-1-dependent mechanism显示文摘Recruitment and retention of circulating progenitor cells at the site of injured or ischemic tissues facilitates adult neovascularization. We hypothesized that cell therapy could modulate local neo-vascularization through the vascular endothelial growth factor(VEGF)/stromal cellderived factor-1(SDF-1) axis and by paracrine effects on local endothelial cells. We isolated from rat bone marrow a subset of multipotent adult progenitor cell-derived progenitor cells(MDPC). In vitro, MDPCs secreted multiple cytokines related to inflammation and angiogenesis, including monocyte chemotactic protein-1, SDF-1, basic fibroblast growth factor, and VEGF, and expressed the chemokine receptors CXCR4 and VEGFR1. To investigate in vivo properties, we transplanted MDPCs into the ischemic hind limbs of rats. Elevated levels of the chemokine SDF-1 and colocalization of cd11b+ cells marked the initial phase of tissue remodeling after cell transplantation. Prolonged engraftment was observed in the adventitial–medial border region of arterioles of ischemic muscles. However, engrafted cells did not differentiate into endothelial or smooth muscle cells. Limb perfusion normalized 4 weeks after cell injection. Inhibition of SDF-1 reduced the engraftment of transplanted cells and decreased endothelial cell proliferation. These findings suggest a two-stage model whereby transplanted MDPCs modulate wound repair through recruitment of inflammatory cells to ischemic tissue. This is an important potential mechanism for cell transplantation, in addition to the direct modulation of local vascular cells through paracrine mechanisms. | Andrew Wragg Jason A.Mellad Leilani E.Beltran Mikhail Konoplyannikov Hong San Sherry Boozer Robert J.deans Anthony Mathur Robert J.lederman Jason C.Kovacic Manfred Boehm | 2015 | 世界最新医学信息文摘2015，15，90： | 0 |
| 9 | VEGFR1/CXCR4-positive progenitor cells modulate local inflammation and augment tissue perfusion by a SDF-1-dependent mechanism显示文摘Recruitment and retention of circulating progenitor cells at the site of injured or ischemic tissues facilitates adult neovascularization.We hypothesized that cell therapy could modulate local neo-vascularization through the vascular endothelial growth factor(VEGF)/stromal cellderived factor-1(SDF-1) axis and by paracrine effects on local endothelial cells.We isolated from rat bone marrow a subset of multipotent adult progenitor cell-derived progenitor cells(MDPC).In vitro,MDPCs secreted multiple cytokines related to inflammation and angiogenesis,including monocyte chemotactic protein-1,SDF-1,basic fibroblast growth factor,and VEGF,and expressed the chemokine receptors CXCR4 and VEGFR1.To investigate in vivo properties,we transplanted MDPCs into the ischemic hind limbs of rats.Elevated levels of the chemokine SDF-1 and colocalization of CD 11b^+ cells marked the initial phase of tissue remodeling after cell transplantation.Prolonged engraftment was observed in the adventitial-medial border region of arterioles of ischemic muscles.However,engrafted cells did not differentiate into endothelial or smooth muscle cells.Limb perfusion normalized 4 weeks after cell injection.Inhibition of SDF-1 reduced the engraftment of transplanted cells and decreased endothelial cell proliferation.These findings suggest a two-stage model whereby transplanted MDPCs modulate wound repair through recruitment of inflammatory cells to ischemic tissue.This is an important potential mechanism for cell transplantation,in addition to the direct modulation of local vascular cells through paracrine mechanisms. | Andrew Wragg Jason A.Mellad Leilani E.Beltran Mikhail Konoplyannikov Hong San Sherry Boozer robert J.deans anthony Mathur Robert J.lederman Jason C.Kovacic Manfred Boehm | 2016 | 世界最新医学信息文摘2016，16，4： | 0 |
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