Multiplex Analysis of Cytokines, Chemokines, Growth Factors, MMP-9 and TIMP-1 Produced by Human Bone Marrow, Adipose Tissue, and Placental Mesenchymal Stromal Cells
Comparative analysis of mesenchymal stromal cells isolated from human BM, adipose tissue, and placenta was carried out. The cells were compared by the levels of constitutive, spontaneous, and LPS-induced production of Th1/proinflammatory (IFN-γ, IL-2, IL-1β, TNF-α, IL-12, IL-17) and Th2/anti-inflamm...
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| Veröffentlicht in: | Bulletin of experimental biology and medicine 2011-05, Vol.151 (1), p.133-141 |
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| creator | Ostanin, A. A. Petrovskii, Ya. L. Shevela, E. Ya Chernykh, E. R. |
| description | Comparative analysis of mesenchymal stromal cells isolated from human BM, adipose tissue, and placenta was carried out. The cells were compared by the levels of constitutive, spontaneous, and LPS-induced production of Th1/proinflammatory (IFN-γ, IL-2, IL-1β, TNF-α, IL-12, IL-17) and Th2/anti-inflammatory cytokines (IL-4, IL-5, IL-6, IL-10, IL-13), chemokines (IL-8, MCP-1, MIP-1β), growth factors (IL-7, granulocytic CSF, granulocytic macrophageal CSF, erythropoietin, VEGF, EGF, IGF-1, main FGF), matrix metalloproteinase-9, and tissue inhibitor of metalloproteinase-1. Mesenchymal stromal cells originating from different tissues were characterized by functional potential for hemopoiesis support (through production of granulocytic CSF, granulocytic macrophage CSF, erythropoietin), immunomodulation (through production of IFN-γ, IL-2, IL-6, IL-1β, TNF-α and chemokines IL-8, MCP-1, MIP-1β), and stimulation of reparative processes (through production of VEGF, FGF, IGF-1, IL-6, tissue inhibitor of metalloproteinase-1, and matrix metalloproteinase-9). By the type and levels of spontaneous (basal) production of cytokines, the adipose tissue mesenchymal stromal cells more distinctly demonstrated the proinflammatory (IL-1β, TNF-α), immunoregulatory (IFN-γ, IL-2, IL-4, IL-6, IL-8, MCP-1, MIP-1β), and hemopoiesis-stimulating (granulocytic CSF, granulocytic macrophage CSF) phenotype and at the same time were characterized by lower sensitivity to lipopolysaccharide stimulation than BM and placental mesenchymal cells. |
| doi_str_mv | 10.1007/s10517-011-1275-2 |
| format | Article |
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A. ; Petrovskii, Ya. L. ; Shevela, E. Ya ; Chernykh, E. R.</creator><creatorcontrib>Ostanin, A. A. ; Petrovskii, Ya. L. ; Shevela, E. Ya ; Chernykh, E. R.</creatorcontrib><description>Comparative analysis of mesenchymal stromal cells isolated from human BM, adipose tissue, and placenta was carried out. The cells were compared by the levels of constitutive, spontaneous, and LPS-induced production of Th1/proinflammatory (IFN-γ, IL-2, IL-1β, TNF-α, IL-12, IL-17) and Th2/anti-inflammatory cytokines (IL-4, IL-5, IL-6, IL-10, IL-13), chemokines (IL-8, MCP-1, MIP-1β), growth factors (IL-7, granulocytic CSF, granulocytic macrophageal CSF, erythropoietin, VEGF, EGF, IGF-1, main FGF), matrix metalloproteinase-9, and tissue inhibitor of metalloproteinase-1. Mesenchymal stromal cells originating from different tissues were characterized by functional potential for hemopoiesis support (through production of granulocytic CSF, granulocytic macrophage CSF, erythropoietin), immunomodulation (through production of IFN-γ, IL-2, IL-6, IL-1β, TNF-α and chemokines IL-8, MCP-1, MIP-1β), and stimulation of reparative processes (through production of VEGF, FGF, IGF-1, IL-6, tissue inhibitor of metalloproteinase-1, and matrix metalloproteinase-9). By the type and levels of spontaneous (basal) production of cytokines, the adipose tissue mesenchymal stromal cells more distinctly demonstrated the proinflammatory (IL-1β, TNF-α), immunoregulatory (IFN-γ, IL-2, IL-4, IL-6, IL-8, MCP-1, MIP-1β), and hemopoiesis-stimulating (granulocytic CSF, granulocytic macrophage CSF) phenotype and at the same time were characterized by lower sensitivity to lipopolysaccharide stimulation than BM and placental mesenchymal cells.</description><identifier>ISSN: 0007-4888</identifier><identifier>EISSN: 1573-8221</identifier><identifier>DOI: 10.1007/s10517-011-1275-2</identifier><identifier>PMID: 22442819</identifier><identifier>CODEN: BEXBAN</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Adipose tissue ; Adipose Tissue - cytology ; Adipose Tissue - metabolism ; Adipose tissues ; Analysis ; Biomedical and Life Sciences ; Biomedicine ; Body fat ; Bone Marrow - metabolism ; Cell Biology ; Chemokines - biosynthesis ; Epidermal growth factor ; Erythropoietin ; Female ; Humans ; Intercellular Signaling Peptides and Proteins - biosynthesis ; Interferon ; Internal Medicine ; Laboratory Medicine ; Lipopolysaccharides - pharmacology ; Matrix Metalloproteinase 9 - biosynthesis ; Mesenchymal Stem Cells - drug effects ; Mesenchymal Stem Cells - metabolism ; Mitogens ; Pathology ; Placenta - cytology ; Placenta - metabolism ; Pregnancy ; Th1-Th2 Balance - drug effects ; Tissue Inhibitor of Metalloproteinase-1 - biosynthesis ; Translated from Kletochnye Tekhnologii v Biologii i Meditsine (Cell Technologies in Biology and Medicine) ; Tumor necrosis factor ; Vascular endothelial growth factor</subject><ispartof>Bulletin of experimental biology and medicine, 2011-05, Vol.151 (1), p.133-141</ispartof><rights>Springer Science+Business Media, Inc. 2011</rights><rights>COPYRIGHT 2011 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-f08d186e4dad9c5fdd924c34d53168d5c595d82635eb0a396699f757ca9e29923</citedby><cites>FETCH-LOGICAL-c501t-f08d186e4dad9c5fdd924c34d53168d5c595d82635eb0a396699f757ca9e29923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10517-011-1275-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10517-011-1275-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22442819$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ostanin, A. A.</creatorcontrib><creatorcontrib>Petrovskii, Ya. L.</creatorcontrib><creatorcontrib>Shevela, E. Ya</creatorcontrib><creatorcontrib>Chernykh, E. R.</creatorcontrib><title>Multiplex Analysis of Cytokines, Chemokines, Growth Factors, MMP-9 and TIMP-1 Produced by Human Bone Marrow, Adipose Tissue, and Placental Mesenchymal Stromal Cells</title><title>Bulletin of experimental biology and medicine</title><addtitle>Bull Exp Biol Med</addtitle><addtitle>Bull Exp Biol Med</addtitle><description>Comparative analysis of mesenchymal stromal cells isolated from human BM, adipose tissue, and placenta was carried out. The cells were compared by the levels of constitutive, spontaneous, and LPS-induced production of Th1/proinflammatory (IFN-γ, IL-2, IL-1β, TNF-α, IL-12, IL-17) and Th2/anti-inflammatory cytokines (IL-4, IL-5, IL-6, IL-10, IL-13), chemokines (IL-8, MCP-1, MIP-1β), growth factors (IL-7, granulocytic CSF, granulocytic macrophageal CSF, erythropoietin, VEGF, EGF, IGF-1, main FGF), matrix metalloproteinase-9, and tissue inhibitor of metalloproteinase-1. Mesenchymal stromal cells originating from different tissues were characterized by functional potential for hemopoiesis support (through production of granulocytic CSF, granulocytic macrophage CSF, erythropoietin), immunomodulation (through production of IFN-γ, IL-2, IL-6, IL-1β, TNF-α and chemokines IL-8, MCP-1, MIP-1β), and stimulation of reparative processes (through production of VEGF, FGF, IGF-1, IL-6, tissue inhibitor of metalloproteinase-1, and matrix metalloproteinase-9). By the type and levels of spontaneous (basal) production of cytokines, the adipose tissue mesenchymal stromal cells more distinctly demonstrated the proinflammatory (IL-1β, TNF-α), immunoregulatory (IFN-γ, IL-2, IL-4, IL-6, IL-8, MCP-1, MIP-1β), and hemopoiesis-stimulating (granulocytic CSF, granulocytic macrophage CSF) phenotype and at the same time were characterized by lower sensitivity to lipopolysaccharide stimulation than BM and placental mesenchymal cells.</description><subject>Adipose tissue</subject><subject>Adipose Tissue - cytology</subject><subject>Adipose Tissue - metabolism</subject><subject>Adipose tissues</subject><subject>Analysis</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Body fat</subject><subject>Bone Marrow - metabolism</subject><subject>Cell Biology</subject><subject>Chemokines - biosynthesis</subject><subject>Epidermal growth factor</subject><subject>Erythropoietin</subject><subject>Female</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins - biosynthesis</subject><subject>Interferon</subject><subject>Internal Medicine</subject><subject>Laboratory Medicine</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Matrix Metalloproteinase 9 - biosynthesis</subject><subject>Mesenchymal Stem Cells - drug effects</subject><subject>Mesenchymal Stem Cells - metabolism</subject><subject>Mitogens</subject><subject>Pathology</subject><subject>Placenta - cytology</subject><subject>Placenta - metabolism</subject><subject>Pregnancy</subject><subject>Th1-Th2 Balance - drug effects</subject><subject>Tissue Inhibitor of Metalloproteinase-1 - biosynthesis</subject><subject>Translated from Kletochnye Tekhnologii v Biologii i Meditsine (Cell Technologies in Biology and Medicine)</subject><subject>Tumor necrosis factor</subject><subject>Vascular endothelial growth factor</subject><issn>0007-4888</issn><issn>1573-8221</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9ktuO0zAQhiMEYkvhAbhBFkjARbPYTpzYl6ViD9JWVKJcW6492WZx4mI7gr4PD4pD98AiQL7wjP39o_H4z7LnBB8TjOt3gWBG6hwTkhNas5w-yCaE1UXOKSUPswlOUF5yzo-yJyFcjSmuyOPsiNKypJyISfZjOdjY7ix8R_Ne2X1oA3INWuyj-9L2EGZosYXuJj717lvcohOlo_MpXy5XuUCqN2h9nkKCVt6ZQYNBmz06GzrVo_euB7RUPilnaG7anQuA1m0IA8x-KVdWaeijsmgJAXq93Xcp_hS9G_cFWBueZo8aZQM8u96n2eeTD-vFWX7x8fR8Mb_INcMk5g3mhvAKSqOM0KwxRtBSF6VhBam4YZoJZjitCgYbrApRVUI0Nau1EkCFoMU0e3Oou_Pu6wAhyq4NOnWgenBDkCLNUuCCkUS-_S9JyqpkuOQ1TujLP9ArN_g06yB5JWpelOnHptmrA3SpLMi2b1z0So815bxgqeOiJmN_x3-h0jLQtToNumnT-T3B698EW1A2boOzQ2xdH-6D5ABq70Lw0Midbzvl95JgOXpNHrwmk9fk6DU5al5cP2zYdGBuFTfmSgA9ACFd9Zfg717-76o_AY_o2tA</recordid><startdate>20110501</startdate><enddate>20110501</enddate><creator>Ostanin, A. A.</creator><creator>Petrovskii, Ya. L.</creator><creator>Shevela, E. Ya</creator><creator>Chernykh, E. 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A. ; Petrovskii, Ya. L. ; Shevela, E. Ya ; Chernykh, E. R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-f08d186e4dad9c5fdd924c34d53168d5c595d82635eb0a396699f757ca9e29923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adipose tissue</topic><topic>Adipose Tissue - cytology</topic><topic>Adipose Tissue - metabolism</topic><topic>Adipose tissues</topic><topic>Analysis</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Body fat</topic><topic>Bone Marrow - metabolism</topic><topic>Cell Biology</topic><topic>Chemokines - biosynthesis</topic><topic>Epidermal growth factor</topic><topic>Erythropoietin</topic><topic>Female</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins - biosynthesis</topic><topic>Interferon</topic><topic>Internal Medicine</topic><topic>Laboratory Medicine</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Matrix Metalloproteinase 9 - biosynthesis</topic><topic>Mesenchymal Stem Cells - drug effects</topic><topic>Mesenchymal Stem Cells - metabolism</topic><topic>Mitogens</topic><topic>Pathology</topic><topic>Placenta - cytology</topic><topic>Placenta - metabolism</topic><topic>Pregnancy</topic><topic>Th1-Th2 Balance - drug effects</topic><topic>Tissue Inhibitor of Metalloproteinase-1 - biosynthesis</topic><topic>Translated from Kletochnye Tekhnologii v Biologii i Meditsine (Cell Technologies in Biology and Medicine)</topic><topic>Tumor necrosis factor</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ostanin, A. A.</creatorcontrib><creatorcontrib>Petrovskii, Ya. L.</creatorcontrib><creatorcontrib>Shevela, E. Ya</creatorcontrib><creatorcontrib>Chernykh, E. 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A.</au><au>Petrovskii, Ya. L.</au><au>Shevela, E. Ya</au><au>Chernykh, E. R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiplex Analysis of Cytokines, Chemokines, Growth Factors, MMP-9 and TIMP-1 Produced by Human Bone Marrow, Adipose Tissue, and Placental Mesenchymal Stromal Cells</atitle><jtitle>Bulletin of experimental biology and medicine</jtitle><stitle>Bull Exp Biol Med</stitle><addtitle>Bull Exp Biol Med</addtitle><date>2011-05-01</date><risdate>2011</risdate><volume>151</volume><issue>1</issue><spage>133</spage><epage>141</epage><pages>133-141</pages><issn>0007-4888</issn><eissn>1573-8221</eissn><coden>BEXBAN</coden><abstract>Comparative analysis of mesenchymal stromal cells isolated from human BM, adipose tissue, and placenta was carried out. The cells were compared by the levels of constitutive, spontaneous, and LPS-induced production of Th1/proinflammatory (IFN-γ, IL-2, IL-1β, TNF-α, IL-12, IL-17) and Th2/anti-inflammatory cytokines (IL-4, IL-5, IL-6, IL-10, IL-13), chemokines (IL-8, MCP-1, MIP-1β), growth factors (IL-7, granulocytic CSF, granulocytic macrophageal CSF, erythropoietin, VEGF, EGF, IGF-1, main FGF), matrix metalloproteinase-9, and tissue inhibitor of metalloproteinase-1. Mesenchymal stromal cells originating from different tissues were characterized by functional potential for hemopoiesis support (through production of granulocytic CSF, granulocytic macrophage CSF, erythropoietin), immunomodulation (through production of IFN-γ, IL-2, IL-6, IL-1β, TNF-α and chemokines IL-8, MCP-1, MIP-1β), and stimulation of reparative processes (through production of VEGF, FGF, IGF-1, IL-6, tissue inhibitor of metalloproteinase-1, and matrix metalloproteinase-9). By the type and levels of spontaneous (basal) production of cytokines, the adipose tissue mesenchymal stromal cells more distinctly demonstrated the proinflammatory (IL-1β, TNF-α), immunoregulatory (IFN-γ, IL-2, IL-4, IL-6, IL-8, MCP-1, MIP-1β), and hemopoiesis-stimulating (granulocytic CSF, granulocytic macrophage CSF) phenotype and at the same time were characterized by lower sensitivity to lipopolysaccharide stimulation than BM and placental mesenchymal cells.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>22442819</pmid><doi>10.1007/s10517-011-1275-2</doi><tpages>9</tpages></addata></record> |
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| subjects | Adipose tissue Adipose Tissue - cytology Adipose Tissue - metabolism Adipose tissues Analysis Biomedical and Life Sciences Biomedicine Body fat Bone Marrow - metabolism Cell Biology Chemokines - biosynthesis Epidermal growth factor Erythropoietin Female Humans Intercellular Signaling Peptides and Proteins - biosynthesis Interferon Internal Medicine Laboratory Medicine Lipopolysaccharides - pharmacology Matrix Metalloproteinase 9 - biosynthesis Mesenchymal Stem Cells - drug effects Mesenchymal Stem Cells - metabolism Mitogens Pathology Placenta - cytology Placenta - metabolism Pregnancy Th1-Th2 Balance - drug effects Tissue Inhibitor of Metalloproteinase-1 - biosynthesis Translated from Kletochnye Tekhnologii v Biologii i Meditsine (Cell Technologies in Biology and Medicine) Tumor necrosis factor Vascular endothelial growth factor |
| title | Multiplex Analysis of Cytokines, Chemokines, Growth Factors, MMP-9 and TIMP-1 Produced by Human Bone Marrow, Adipose Tissue, and Placental Mesenchymal Stromal Cells |
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