Human adipose tissue stromal vascular fraction cells differentiate depending on distinct types of media

.  Objectives: Angiogenesis, the process of formation of blood vessels, is essential for many physiological as well as pathological processes. It has been shown that human adipose tissue contains a population of non‐characterized cells, called stromal‐vascular fraction (SVF) cells, which are able to...

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Veröffentlicht in:Cell proliferation 2008-06, Vol.41 (3), p.441-459
Hauptverfasser: Balwierz, A., Czech, U., Polus, A., Filipkowski, R. K., Mioduszewska, B., Proszynski, T., Kolodziejczyk, P., Skrzeczynska-Moncznik, J., Dudek, W., Kaczmarek, L., Kulig, J., Pryjma, J., Dembinska-Kiec, A.
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container_end_page 459
container_issue 3
container_start_page 441
container_title Cell proliferation
container_volume 41
creator Balwierz, A.
Czech, U.
Polus, A.
Filipkowski, R. K.
Mioduszewska, B.
Proszynski, T.
Kolodziejczyk, P.
Skrzeczynska-Moncznik, J.
Dudek, W.
Kaczmarek, L.
Kulig, J.
Pryjma, J.
Dembinska-Kiec, A.
description .  Objectives: Angiogenesis, the process of formation of blood vessels, is essential for many physiological as well as pathological processes. It has been shown that human adipose tissue contains a population of non‐characterized cells, called stromal‐vascular fraction (SVF) cells, which are able to differentiate into several lineages. The aim of this study was to determine conditions for promoting differentiation of human adipose tissue progenitors towards endothelial cells, as well as to show that SVF cells cooperate with differentiated endothelium in capillary network formation. Materials and methods: Stromal vascular fraction cells were isolated according to modified Hauner's method and after adaptation they were cultured in pro‐angiogenic or pro‐adipogenic medium. Cells were characterized by presence of surface antigens by flow cytometry, and by expression of genes characteristic for endothelial cells or for adipocytes, quantitative real‐time polymerase chain reaction. A number of tests were performed to verify their differentiation. Results: Differentiation of human SVF cells towards endothelium was stimulated by the presence of serum and absence of adipogenic factors, documented by the pattern of gene expression as well as different functional in vitro assays. SVF cells were found to work together with human umbilical vein endothelial cells to form capillary networks. Conclusions: Here, we show that differentiation of SVF cells to endothelial cells or adipocyte‐like cells depended on the medium used. Our work provides a clear model for analysing the differentiation capacity of SVF cells.
doi_str_mv 10.1111/j.1365-2184.2008.00531.x
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K. ; Mioduszewska, B. ; Proszynski, T. ; Kolodziejczyk, P. ; Skrzeczynska-Moncznik, J. ; Dudek, W. ; Kaczmarek, L. ; Kulig, J. ; Pryjma, J. ; Dembinska-Kiec, A.</creator><creatorcontrib>Balwierz, A. ; Czech, U. ; Polus, A. ; Filipkowski, R. K. ; Mioduszewska, B. ; Proszynski, T. ; Kolodziejczyk, P. ; Skrzeczynska-Moncznik, J. ; Dudek, W. ; Kaczmarek, L. ; Kulig, J. ; Pryjma, J. ; Dembinska-Kiec, A.</creatorcontrib><description>.  Objectives: Angiogenesis, the process of formation of blood vessels, is essential for many physiological as well as pathological processes. It has been shown that human adipose tissue contains a population of non‐characterized cells, called stromal‐vascular fraction (SVF) cells, which are able to differentiate into several lineages. The aim of this study was to determine conditions for promoting differentiation of human adipose tissue progenitors towards endothelial cells, as well as to show that SVF cells cooperate with differentiated endothelium in capillary network formation. Materials and methods: Stromal vascular fraction cells were isolated according to modified Hauner's method and after adaptation they were cultured in pro‐angiogenic or pro‐adipogenic medium. Cells were characterized by presence of surface antigens by flow cytometry, and by expression of genes characteristic for endothelial cells or for adipocytes, quantitative real‐time polymerase chain reaction. A number of tests were performed to verify their differentiation. Results: Differentiation of human SVF cells towards endothelium was stimulated by the presence of serum and absence of adipogenic factors, documented by the pattern of gene expression as well as different functional in vitro assays. SVF cells were found to work together with human umbilical vein endothelial cells to form capillary networks. Conclusions: Here, we show that differentiation of SVF cells to endothelial cells or adipocyte‐like cells depended on the medium used. 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The aim of this study was to determine conditions for promoting differentiation of human adipose tissue progenitors towards endothelial cells, as well as to show that SVF cells cooperate with differentiated endothelium in capillary network formation. Materials and methods: Stromal vascular fraction cells were isolated according to modified Hauner's method and after adaptation they were cultured in pro‐angiogenic or pro‐adipogenic medium. Cells were characterized by presence of surface antigens by flow cytometry, and by expression of genes characteristic for endothelial cells or for adipocytes, quantitative real‐time polymerase chain reaction. A number of tests were performed to verify their differentiation. Results: Differentiation of human SVF cells towards endothelium was stimulated by the presence of serum and absence of adipogenic factors, documented by the pattern of gene expression as well as different functional in vitro assays. SVF cells were found to work together with human umbilical vein endothelial cells to form capillary networks. Conclusions: Here, we show that differentiation of SVF cells to endothelial cells or adipocyte‐like cells depended on the medium used. 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K. ; Mioduszewska, B. ; Proszynski, T. ; Kolodziejczyk, P. ; Skrzeczynska-Moncznik, J. ; Dudek, W. ; Kaczmarek, L. ; Kulig, J. ; Pryjma, J. ; Dembinska-Kiec, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5751-9e6f0a00e2884a4cb93f8f802efd4a798038abc45e8e59b8501f4b9672bf71dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adipocytes - cytology</topic><topic>Adipose Tissue - cytology</topic><topic>Adult</topic><topic>Blood Vessels - cytology</topic><topic>Capillaries - cytology</topic><topic>Cell Differentiation</topic><topic>Cell Movement</topic><topic>Cell Proliferation</topic><topic>Cell Separation</topic><topic>Cells, Cultured</topic><topic>Collagen - metabolism</topic><topic>Culture Media - metabolism</topic><topic>Culture Media, Serum-Free</topic><topic>Drug Combinations</topic><topic>Female</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>Laminin - metabolism</topic><topic>Middle Aged</topic><topic>Neovascularization, Physiologic</topic><topic>Original</topic><topic>Proteoglycans - metabolism</topic><topic>Stromal Cells - cytology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Balwierz, A.</creatorcontrib><creatorcontrib>Czech, U.</creatorcontrib><creatorcontrib>Polus, A.</creatorcontrib><creatorcontrib>Filipkowski, R. K.</creatorcontrib><creatorcontrib>Mioduszewska, B.</creatorcontrib><creatorcontrib>Proszynski, T.</creatorcontrib><creatorcontrib>Kolodziejczyk, P.</creatorcontrib><creatorcontrib>Skrzeczynska-Moncznik, J.</creatorcontrib><creatorcontrib>Dudek, W.</creatorcontrib><creatorcontrib>Kaczmarek, L.</creatorcontrib><creatorcontrib>Kulig, J.</creatorcontrib><creatorcontrib>Pryjma, J.</creatorcontrib><creatorcontrib>Dembinska-Kiec, A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell proliferation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Balwierz, A.</au><au>Czech, U.</au><au>Polus, A.</au><au>Filipkowski, R. K.</au><au>Mioduszewska, B.</au><au>Proszynski, T.</au><au>Kolodziejczyk, P.</au><au>Skrzeczynska-Moncznik, J.</au><au>Dudek, W.</au><au>Kaczmarek, L.</au><au>Kulig, J.</au><au>Pryjma, J.</au><au>Dembinska-Kiec, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human adipose tissue stromal vascular fraction cells differentiate depending on distinct types of media</atitle><jtitle>Cell proliferation</jtitle><addtitle>Cell Prolif</addtitle><date>2008-06</date><risdate>2008</risdate><volume>41</volume><issue>3</issue><spage>441</spage><epage>459</epage><pages>441-459</pages><issn>0960-7722</issn><eissn>1365-2184</eissn><abstract>.  Objectives: Angiogenesis, the process of formation of blood vessels, is essential for many physiological as well as pathological processes. It has been shown that human adipose tissue contains a population of non‐characterized cells, called stromal‐vascular fraction (SVF) cells, which are able to differentiate into several lineages. The aim of this study was to determine conditions for promoting differentiation of human adipose tissue progenitors towards endothelial cells, as well as to show that SVF cells cooperate with differentiated endothelium in capillary network formation. Materials and methods: Stromal vascular fraction cells were isolated according to modified Hauner's method and after adaptation they were cultured in pro‐angiogenic or pro‐adipogenic medium. Cells were characterized by presence of surface antigens by flow cytometry, and by expression of genes characteristic for endothelial cells or for adipocytes, quantitative real‐time polymerase chain reaction. A number of tests were performed to verify their differentiation. Results: Differentiation of human SVF cells towards endothelium was stimulated by the presence of serum and absence of adipogenic factors, documented by the pattern of gene expression as well as different functional in vitro assays. SVF cells were found to work together with human umbilical vein endothelial cells to form capillary networks. Conclusions: Here, we show that differentiation of SVF cells to endothelial cells or adipocyte‐like cells depended on the medium used. Our work provides a clear model for analysing the differentiation capacity of SVF cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18422701</pmid><doi>10.1111/j.1365-2184.2008.00531.x</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record>
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subjects Adipocytes - cytology
Adipose Tissue - cytology
Adult
Blood Vessels - cytology
Capillaries - cytology
Cell Differentiation
Cell Movement
Cell Proliferation
Cell Separation
Cells, Cultured
Collagen - metabolism
Culture Media - metabolism
Culture Media, Serum-Free
Drug Combinations
Female
Gene Expression Regulation
Humans
Laminin - metabolism
Middle Aged
Neovascularization, Physiologic
Original
Proteoglycans - metabolism
Stromal Cells - cytology
Time Factors
title Human adipose tissue stromal vascular fraction cells differentiate depending on distinct types of media
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