Proliferation of ASC-derived endothelial cells in a 3D electrospun mesh: Impact of bone-biomimetic nanocomposite and co-culture with ASC-derived osteoblasts
Abstract Background Fractures with a critical size bone defect are associated with high rates of delayed- and non-union. The treatment of such complications remains a serious issue in orthopaedic surgery. Adipose derived stem cells (ASCs) combined with biomimetic materials can potentially be used to...
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Veröffentlicht in: | Injury 2014-06, Vol.45 (6), p.974-980 |
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creator | Gao, Shuping Calcagni, Maurizio Welti, Manfred Hemmi, Sonja Hild, Nora Stark, Wendelin J Meier Bürgisser, Gabriella Wanner, Guido A Cinelli, Paolo Buschmann, Johanna |
description | Abstract Background Fractures with a critical size bone defect are associated with high rates of delayed- and non-union. The treatment of such complications remains a serious issue in orthopaedic surgery. Adipose derived stem cells (ASCs) combined with biomimetic materials can potentially be used to increase fracture healing. Nevertheless, a number of requirements have to be fulfilled; in particular, the insufficient vascularisation of the bone constructs. Here, the objectives were to study the impact of ASC-derived osteoblasts on ASC-derived endothelial cells in a 3D co-culture and the effect of 40 wt% of amorphous calcium phosphate nanoparticles on the proliferation and differentiation of ASC-derived endothelial cells when present in PLGA. Materials and methods Five primary ASC lines were differentiated towards osteoblasts (OBs) and endothelial cells (ECs) and two of them were chosen based on quantitative PCR results. Either a mono-culture of ASC-derived EC or a co-culture of ASC-derived EC with ASC-derived OB (1:1) was seeded on an electrospun nanocomposite of poly-(lactic-co-glycolic acid) and amorphous calcium phosphate nanoparticles (PLGA/a-CaP; reference: PLGA). The proliferation behaviour was determined histomorphometrically in different zones and the expression of von Willebrand Factor (vWF) was quantified. Results Independently of the fat source (biologic variability), ASC-derived osteoblasts decelerated the proliferation behaviour of ASC-derived endothelial cells in the co-culture compared to the mono-culture. However, expression of vWF was clearly stronger in the co-culture, indicating further differentiation of the ASC-derived EC into the EC lineage. Moreover, the presence of a-CaP nanoparticles in the scaffold slowed the proliferation behaviour of the co-culture cells, too, going along with a further differentiation of the ASC-derived OB, when compared to pure PLGA scaffolds. Conclusions This study revealed significant findings for bone tissue-engineering. Co-cultures of ASC-derived EC and ASC-derived OB stimulate each other's further differentiation. A nanocomposite with a-CaP nanoparticles offers higher mechanical stability, bioactivity and osteoconductivity compared to mere PLGA and can easily be seeded with pre-differentiated EC and OB. |
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The treatment of such complications remains a serious issue in orthopaedic surgery. Adipose derived stem cells (ASCs) combined with biomimetic materials can potentially be used to increase fracture healing. Nevertheless, a number of requirements have to be fulfilled; in particular, the insufficient vascularisation of the bone constructs. Here, the objectives were to study the impact of ASC-derived osteoblasts on ASC-derived endothelial cells in a 3D co-culture and the effect of 40 wt% of amorphous calcium phosphate nanoparticles on the proliferation and differentiation of ASC-derived endothelial cells when present in PLGA. Materials and methods Five primary ASC lines were differentiated towards osteoblasts (OBs) and endothelial cells (ECs) and two of them were chosen based on quantitative PCR results. Either a mono-culture of ASC-derived EC or a co-culture of ASC-derived EC with ASC-derived OB (1:1) was seeded on an electrospun nanocomposite of poly-(lactic-co-glycolic acid) and amorphous calcium phosphate nanoparticles (PLGA/a-CaP; reference: PLGA). The proliferation behaviour was determined histomorphometrically in different zones and the expression of von Willebrand Factor (vWF) was quantified. Results Independently of the fat source (biologic variability), ASC-derived osteoblasts decelerated the proliferation behaviour of ASC-derived endothelial cells in the co-culture compared to the mono-culture. However, expression of vWF was clearly stronger in the co-culture, indicating further differentiation of the ASC-derived EC into the EC lineage. Moreover, the presence of a-CaP nanoparticles in the scaffold slowed the proliferation behaviour of the co-culture cells, too, going along with a further differentiation of the ASC-derived OB, when compared to pure PLGA scaffolds. Conclusions This study revealed significant findings for bone tissue-engineering. Co-cultures of ASC-derived EC and ASC-derived OB stimulate each other's further differentiation. A nanocomposite with a-CaP nanoparticles offers higher mechanical stability, bioactivity and osteoconductivity compared to mere PLGA and can easily be seeded with pre-differentiated EC and OB.</description><identifier>ISSN: 0020-1383</identifier><identifier>EISSN: 1879-0267</identifier><identifier>DOI: 10.1016/j.injury.2014.02.035</identifier><identifier>PMID: 24650943</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adipose Tissue - cytology ; Adipose-derived stem cell ; Amorphous calcium phosphate ; Biological effects ; Biomechanical Phenomena ; Biomimetic Materials ; Bone ; Bones ; Calcium Phosphates - metabolism ; Cell Differentiation ; Cell Line ; Cell Proliferation ; Cells, Cultured ; Co-culture ; Coculture Techniques ; Composite ; Differentiation ; Endothelial cells ; Endothelial Cells - cytology ; Endothelial Cells - metabolism ; Fractures, Bone - pathology ; Fractures, Ununited - pathology ; Humans ; Nanocomposites ; Nanoparticle ; Nanoparticles ; Nanostructure ; Orthopedics ; Osteoblasts ; Osteoblasts - cytology ; Osteoblasts - metabolism ; Osteogenesis ; PLGA ; Stem Cells ; Three dimensional ; Tissue Engineering - methods ; Tissue Scaffolds</subject><ispartof>Injury, 2014-06, Vol.45 (6), p.974-980</ispartof><rights>Elsevier Ltd</rights><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-6823cbf83802929f37e2cc75fcc6accb8d81a5a6a3384c720df66423ac6a9a5a3</citedby><cites>FETCH-LOGICAL-c450t-6823cbf83802929f37e2cc75fcc6accb8d81a5a6a3384c720df66423ac6a9a5a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.injury.2014.02.035$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24650943$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Shuping</creatorcontrib><creatorcontrib>Calcagni, Maurizio</creatorcontrib><creatorcontrib>Welti, Manfred</creatorcontrib><creatorcontrib>Hemmi, Sonja</creatorcontrib><creatorcontrib>Hild, Nora</creatorcontrib><creatorcontrib>Stark, Wendelin J</creatorcontrib><creatorcontrib>Meier Bürgisser, Gabriella</creatorcontrib><creatorcontrib>Wanner, Guido A</creatorcontrib><creatorcontrib>Cinelli, Paolo</creatorcontrib><creatorcontrib>Buschmann, Johanna</creatorcontrib><title>Proliferation of ASC-derived endothelial cells in a 3D electrospun mesh: Impact of bone-biomimetic nanocomposite and co-culture with ASC-derived osteoblasts</title><title>Injury</title><addtitle>Injury</addtitle><description>Abstract Background Fractures with a critical size bone defect are associated with high rates of delayed- and non-union. The treatment of such complications remains a serious issue in orthopaedic surgery. Adipose derived stem cells (ASCs) combined with biomimetic materials can potentially be used to increase fracture healing. Nevertheless, a number of requirements have to be fulfilled; in particular, the insufficient vascularisation of the bone constructs. Here, the objectives were to study the impact of ASC-derived osteoblasts on ASC-derived endothelial cells in a 3D co-culture and the effect of 40 wt% of amorphous calcium phosphate nanoparticles on the proliferation and differentiation of ASC-derived endothelial cells when present in PLGA. Materials and methods Five primary ASC lines were differentiated towards osteoblasts (OBs) and endothelial cells (ECs) and two of them were chosen based on quantitative PCR results. Either a mono-culture of ASC-derived EC or a co-culture of ASC-derived EC with ASC-derived OB (1:1) was seeded on an electrospun nanocomposite of poly-(lactic-co-glycolic acid) and amorphous calcium phosphate nanoparticles (PLGA/a-CaP; reference: PLGA). The proliferation behaviour was determined histomorphometrically in different zones and the expression of von Willebrand Factor (vWF) was quantified. Results Independently of the fat source (biologic variability), ASC-derived osteoblasts decelerated the proliferation behaviour of ASC-derived endothelial cells in the co-culture compared to the mono-culture. However, expression of vWF was clearly stronger in the co-culture, indicating further differentiation of the ASC-derived EC into the EC lineage. Moreover, the presence of a-CaP nanoparticles in the scaffold slowed the proliferation behaviour of the co-culture cells, too, going along with a further differentiation of the ASC-derived OB, when compared to pure PLGA scaffolds. Conclusions This study revealed significant findings for bone tissue-engineering. Co-cultures of ASC-derived EC and ASC-derived OB stimulate each other's further differentiation. A nanocomposite with a-CaP nanoparticles offers higher mechanical stability, bioactivity and osteoconductivity compared to mere PLGA and can easily be seeded with pre-differentiated EC and OB.</description><subject>Adipose Tissue - cytology</subject><subject>Adipose-derived stem cell</subject><subject>Amorphous calcium phosphate</subject><subject>Biological effects</subject><subject>Biomechanical Phenomena</subject><subject>Biomimetic Materials</subject><subject>Bone</subject><subject>Bones</subject><subject>Calcium Phosphates - metabolism</subject><subject>Cell Differentiation</subject><subject>Cell Line</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>Co-culture</subject><subject>Coculture Techniques</subject><subject>Composite</subject><subject>Differentiation</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - cytology</subject><subject>Endothelial Cells - metabolism</subject><subject>Fractures, Bone - pathology</subject><subject>Fractures, Ununited - pathology</subject><subject>Humans</subject><subject>Nanocomposites</subject><subject>Nanoparticle</subject><subject>Nanoparticles</subject><subject>Nanostructure</subject><subject>Orthopedics</subject><subject>Osteoblasts</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - metabolism</subject><subject>Osteogenesis</subject><subject>PLGA</subject><subject>Stem Cells</subject><subject>Three dimensional</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds</subject><issn>0020-1383</issn><issn>1879-0267</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUkuL1TAYLaI4d0b_gUiWblrz6NOFMFx1HBhQGAV3If36lZuaJjVJR-5_8ceackdBN7rK4jsPcs7JsmeMFoyy-uVUaDut_lhwysqC8oKK6kG2Y23T5ZTXzcNsRymnOROtOMvOQ5goZQ0V4nF2xsu6ol0pdtmPj94ZPaJXUTtL3Egub_f5gF7f4UDQDi4e0GhlCKAxgWhLFBFvCBqE6F1YVktmDIdX5HpeFMRNoXcW8167Wc8YNRCrrAM3Ly7oiETZgYDLYTVx9Ui-63j4w9OFiK43KsTwJHs0KhPw6f17kX1-9_bT_n1-8-Hqen95k0NZ0ZjXLRfQj61oKe94N4oGOUBTjQC1AujboWWqUrUSoi2h4XQY67rkQqVzlw7iIntx0l28-7ZiiHLWYfuvsujWIFlVMVo1nLP_gLK64VXVNglanqCQcgoeR7l4PSt_lIzKrUI5yVOFcqtQUi5ThYn2_N5h7WccfpN-dZYAr08ATJHcafQygEYLOGifSpGD0_9y-FsAjLYalPmKRwyTW71NcUsmQyLI221G24pYmRbEmi_iJ2RgxhQ</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Gao, Shuping</creator><creator>Calcagni, Maurizio</creator><creator>Welti, Manfred</creator><creator>Hemmi, Sonja</creator><creator>Hild, Nora</creator><creator>Stark, Wendelin J</creator><creator>Meier Bürgisser, Gabriella</creator><creator>Wanner, Guido A</creator><creator>Cinelli, Paolo</creator><creator>Buschmann, Johanna</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QQ</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope></search><sort><creationdate>20140601</creationdate><title>Proliferation of ASC-derived endothelial cells in a 3D electrospun mesh: Impact of bone-biomimetic nanocomposite and co-culture with ASC-derived osteoblasts</title><author>Gao, Shuping ; Calcagni, Maurizio ; Welti, Manfred ; Hemmi, Sonja ; Hild, Nora ; Stark, Wendelin J ; Meier Bürgisser, Gabriella ; Wanner, Guido A ; Cinelli, Paolo ; Buschmann, Johanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-6823cbf83802929f37e2cc75fcc6accb8d81a5a6a3384c720df66423ac6a9a5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adipose Tissue - cytology</topic><topic>Adipose-derived stem cell</topic><topic>Amorphous calcium phosphate</topic><topic>Biological effects</topic><topic>Biomechanical Phenomena</topic><topic>Biomimetic Materials</topic><topic>Bone</topic><topic>Bones</topic><topic>Calcium Phosphates - metabolism</topic><topic>Cell Differentiation</topic><topic>Cell Line</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>Co-culture</topic><topic>Coculture Techniques</topic><topic>Composite</topic><topic>Differentiation</topic><topic>Endothelial cells</topic><topic>Endothelial Cells - cytology</topic><topic>Endothelial Cells - metabolism</topic><topic>Fractures, Bone - pathology</topic><topic>Fractures, Ununited - pathology</topic><topic>Humans</topic><topic>Nanocomposites</topic><topic>Nanoparticle</topic><topic>Nanoparticles</topic><topic>Nanostructure</topic><topic>Orthopedics</topic><topic>Osteoblasts</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - metabolism</topic><topic>Osteogenesis</topic><topic>PLGA</topic><topic>Stem Cells</topic><topic>Three dimensional</topic><topic>Tissue Engineering - methods</topic><topic>Tissue Scaffolds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Shuping</creatorcontrib><creatorcontrib>Calcagni, Maurizio</creatorcontrib><creatorcontrib>Welti, Manfred</creatorcontrib><creatorcontrib>Hemmi, Sonja</creatorcontrib><creatorcontrib>Hild, Nora</creatorcontrib><creatorcontrib>Stark, Wendelin J</creatorcontrib><creatorcontrib>Meier Bürgisser, Gabriella</creatorcontrib><creatorcontrib>Wanner, Guido A</creatorcontrib><creatorcontrib>Cinelli, Paolo</creatorcontrib><creatorcontrib>Buschmann, Johanna</creatorcontrib><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>Ceramic Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Injury</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Shuping</au><au>Calcagni, Maurizio</au><au>Welti, Manfred</au><au>Hemmi, Sonja</au><au>Hild, Nora</au><au>Stark, Wendelin J</au><au>Meier Bürgisser, Gabriella</au><au>Wanner, Guido A</au><au>Cinelli, Paolo</au><au>Buschmann, Johanna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proliferation of ASC-derived endothelial cells in a 3D electrospun mesh: Impact of bone-biomimetic nanocomposite and co-culture with ASC-derived osteoblasts</atitle><jtitle>Injury</jtitle><addtitle>Injury</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>45</volume><issue>6</issue><spage>974</spage><epage>980</epage><pages>974-980</pages><issn>0020-1383</issn><eissn>1879-0267</eissn><abstract>Abstract Background Fractures with a critical size bone defect are associated with high rates of delayed- and non-union. The treatment of such complications remains a serious issue in orthopaedic surgery. Adipose derived stem cells (ASCs) combined with biomimetic materials can potentially be used to increase fracture healing. Nevertheless, a number of requirements have to be fulfilled; in particular, the insufficient vascularisation of the bone constructs. Here, the objectives were to study the impact of ASC-derived osteoblasts on ASC-derived endothelial cells in a 3D co-culture and the effect of 40 wt% of amorphous calcium phosphate nanoparticles on the proliferation and differentiation of ASC-derived endothelial cells when present in PLGA. Materials and methods Five primary ASC lines were differentiated towards osteoblasts (OBs) and endothelial cells (ECs) and two of them were chosen based on quantitative PCR results. Either a mono-culture of ASC-derived EC or a co-culture of ASC-derived EC with ASC-derived OB (1:1) was seeded on an electrospun nanocomposite of poly-(lactic-co-glycolic acid) and amorphous calcium phosphate nanoparticles (PLGA/a-CaP; reference: PLGA). The proliferation behaviour was determined histomorphometrically in different zones and the expression of von Willebrand Factor (vWF) was quantified. Results Independently of the fat source (biologic variability), ASC-derived osteoblasts decelerated the proliferation behaviour of ASC-derived endothelial cells in the co-culture compared to the mono-culture. However, expression of vWF was clearly stronger in the co-culture, indicating further differentiation of the ASC-derived EC into the EC lineage. Moreover, the presence of a-CaP nanoparticles in the scaffold slowed the proliferation behaviour of the co-culture cells, too, going along with a further differentiation of the ASC-derived OB, when compared to pure PLGA scaffolds. Conclusions This study revealed significant findings for bone tissue-engineering. Co-cultures of ASC-derived EC and ASC-derived OB stimulate each other's further differentiation. A nanocomposite with a-CaP nanoparticles offers higher mechanical stability, bioactivity and osteoconductivity compared to mere PLGA and can easily be seeded with pre-differentiated EC and OB.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>24650943</pmid><doi>10.1016/j.injury.2014.02.035</doi><tpages>7</tpages></addata></record> |
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subjects | Adipose Tissue - cytology Adipose-derived stem cell Amorphous calcium phosphate Biological effects Biomechanical Phenomena Biomimetic Materials Bone Bones Calcium Phosphates - metabolism Cell Differentiation Cell Line Cell Proliferation Cells, Cultured Co-culture Coculture Techniques Composite Differentiation Endothelial cells Endothelial Cells - cytology Endothelial Cells - metabolism Fractures, Bone - pathology Fractures, Ununited - pathology Humans Nanocomposites Nanoparticle Nanoparticles Nanostructure Orthopedics Osteoblasts Osteoblasts - cytology Osteoblasts - metabolism Osteogenesis PLGA Stem Cells Three dimensional Tissue Engineering - methods Tissue Scaffolds |
title | Proliferation of ASC-derived endothelial cells in a 3D electrospun mesh: Impact of bone-biomimetic nanocomposite and co-culture with ASC-derived osteoblasts |
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