Morphological dependent effect of cell-free formed supramolecular fibronectin on cellular activities
Fibrillar fibronectin (FFN), an active form of fibronectin (FN), plays important roles in various cellular processes. Our goal is to investigate effect of FFN morphology on cellular behaviors. Plasma FN at two concentrations was cross-linked into FFN by dialysis against 2 M urea followed by morpholo...
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Veröffentlicht in: | Biological chemistry 2021-01, Vol.402 (2), p.155-165 |
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description | Fibrillar fibronectin (FFN), an active form of fibronectin (FN), plays important roles in various cellular processes. Our goal is to investigate effect of FFN morphology on cellular behaviors. Plasma FN at two concentrations was cross-linked into FFN by dialysis against 2 M urea followed by morphological analysis under Scanning Electron Microscopy. To evaluate effect of FFN morphology, fibroblasts were cultured on FN or different FFNs. Fibroblast behaviors including adhesion, spreading, and migration were evaluated. Our data showed that FN fibrillogenesis was dependent on FN concentration. At high concentrations (0.75 mg/mL), large FFN approximately 2.167 + 0.875 µm in diameter were formed with attached nodular structures and rough surface. In contrast, smooth surface FFN fibrils with diameter of 1.886 + 0.412 µm were formed from FN at 0.25 mg/mL. Cellular assays revealed morphological dependent biological effects of different FFNs. Fibroblast separately adhered to native FN and remained spherical while on FFN, cells attached with higher quantity and showed spreading morphology. A synergistic ligand interaction of integrin α5β1 and αvβ3 was observed in cell adhering on FFN. Cell migration results showed that large FFN decreased migration rate while small FFN did not. Taken together, our data draws new attention towards controlling biological function of FN by its fibrillar structure. |
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Our goal is to investigate effect of FFN morphology on cellular behaviors. Plasma FN at two concentrations was cross-linked into FFN by dialysis against 2 M urea followed by morphological analysis under Scanning Electron Microscopy. To evaluate effect of FFN morphology, fibroblasts were cultured on FN or different FFNs. Fibroblast behaviors including adhesion, spreading, and migration were evaluated. Our data showed that FN fibrillogenesis was dependent on FN concentration. At high concentrations (0.75 mg/mL), large FFN approximately 2.167 + 0.875 µm in diameter were formed with attached nodular structures and rough surface. In contrast, smooth surface FFN fibrils with diameter of 1.886 + 0.412 µm were formed from FN at 0.25 mg/mL. Cellular assays revealed morphological dependent biological effects of different FFNs. Fibroblast separately adhered to native FN and remained spherical while on FFN, cells attached with higher quantity and showed spreading morphology. A synergistic ligand interaction of integrin α5β1 and αvβ3 was observed in cell adhering on FFN. Cell migration results showed that large FFN decreased migration rate while small FFN did not. Taken together, our data draws new attention towards controlling biological function of FN by its fibrillar structure.</description><identifier>ISSN: 1431-6730</identifier><identifier>EISSN: 1437-4315</identifier><identifier>DOI: 10.1515/hsz-2019-0402</identifier><identifier>PMID: 33544471</identifier><language>eng</language><publisher>Germany: De Gruyter</publisher><subject>Biological effects ; Cell adhesion & migration ; cell free assembly ; Cell migration ; Cytology ; Dialysis ; fibrillar fibronectin ; Fibrillogenesis ; Fibroblasts ; Fibronectin ; Fibrous structure ; Morphology ; Scanning electron microscopy ; Urea</subject><ispartof>Biological chemistry, 2021-01, Vol.402 (2), p.155-165</ispartof><rights>2020 Walter de Gruyter GmbH, Berlin/Boston.</rights><rights>2020 Walter de Gruyter GmbH, Berlin/Boston</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c374t-772d63304112438245692795b86fcb948229025dbf291cea0103a4b1e5c1113e3</citedby><cites>FETCH-LOGICAL-c374t-772d63304112438245692795b86fcb948229025dbf291cea0103a4b1e5c1113e3</cites><orcidid>0000-0001-5630-0369</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.degruyter.com/document/doi/10.1515/hsz-2019-0402/pdf$$EPDF$$P50$$Gwalterdegruyter$$H</linktopdf><linktohtml>$$Uhttps://www.degruyter.com/document/doi/10.1515/hsz-2019-0402/html$$EHTML$$P50$$Gwalterdegruyter$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,66503,68287</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33544471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Le, Phong</creatorcontrib><creatorcontrib>Mai-Thi, Hoang-Nghi</creatorcontrib><creatorcontrib>Stoldt, Volker R.</creatorcontrib><creatorcontrib>Tran, Ngoc Quyen</creatorcontrib><creatorcontrib>Huynh, Khon</creatorcontrib><title>Morphological dependent effect of cell-free formed supramolecular fibronectin on cellular activities</title><title>Biological chemistry</title><addtitle>Biol Chem</addtitle><description>Fibrillar fibronectin (FFN), an active form of fibronectin (FN), plays important roles in various cellular processes. Our goal is to investigate effect of FFN morphology on cellular behaviors. Plasma FN at two concentrations was cross-linked into FFN by dialysis against 2 M urea followed by morphological analysis under Scanning Electron Microscopy. To evaluate effect of FFN morphology, fibroblasts were cultured on FN or different FFNs. Fibroblast behaviors including adhesion, spreading, and migration were evaluated. Our data showed that FN fibrillogenesis was dependent on FN concentration. At high concentrations (0.75 mg/mL), large FFN approximately 2.167 + 0.875 µm in diameter were formed with attached nodular structures and rough surface. In contrast, smooth surface FFN fibrils with diameter of 1.886 + 0.412 µm were formed from FN at 0.25 mg/mL. Cellular assays revealed morphological dependent biological effects of different FFNs. Fibroblast separately adhered to native FN and remained spherical while on FFN, cells attached with higher quantity and showed spreading morphology. A synergistic ligand interaction of integrin α5β1 and αvβ3 was observed in cell adhering on FFN. Cell migration results showed that large FFN decreased migration rate while small FFN did not. Taken together, our data draws new attention towards controlling biological function of FN by its fibrillar structure.</description><subject>Biological effects</subject><subject>Cell adhesion & migration</subject><subject>cell free assembly</subject><subject>Cell migration</subject><subject>Cytology</subject><subject>Dialysis</subject><subject>fibrillar fibronectin</subject><subject>Fibrillogenesis</subject><subject>Fibroblasts</subject><subject>Fibronectin</subject><subject>Fibrous structure</subject><subject>Morphology</subject><subject>Scanning electron microscopy</subject><subject>Urea</subject><issn>1431-6730</issn><issn>1437-4315</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNptkEtLxTAQRoMovpdupeDGTTSTx00LbkR8geJG1yVNJ9dKb1OTVtFfb-5DBRECGYbDNx-HkANgJ6BAnT7HT8oZFJRJxtfINkihqRSg1hcz0IkWbIvsxPjCGMuZFJtkSwglpdSwTep7H_pn3_ppY02b1dhjV2M3ZOgc2iHzLrPYttQFxMz5MMM6i2MfzMy3aMfWhMw1VfBdgpsu890CX-xN2rw1Q4Nxj2w400bcX_275Onq8vHiht49XN9enN9RK7QcqNa8ngjBJACXIudSTQquC1XlE2erQuacF4yrunK8AIuGARNGVoDKAoBAsUuOl7l98K8jxqGcNXHex3Tox1hymWtQSrM8oUd_0Bc_hi61S5ROl1IDlSi6pGzwMQZ0ZR-amQkfJbByrr9M-su5_nKuP_GHq9SxSqZ-6G_fCThbAu-mHTDUOA3jRxp-r_8bnB5PxcUXmbiTdA</recordid><startdate>20210127</startdate><enddate>20210127</enddate><creator>Le, Phong</creator><creator>Mai-Thi, Hoang-Nghi</creator><creator>Stoldt, Volker R.</creator><creator>Tran, Ngoc Quyen</creator><creator>Huynh, Khon</creator><general>De Gruyter</general><general>Walter de Gruyter GmbH</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5630-0369</orcidid></search><sort><creationdate>20210127</creationdate><title>Morphological dependent effect of cell-free formed supramolecular fibronectin on cellular activities</title><author>Le, Phong ; Mai-Thi, Hoang-Nghi ; Stoldt, Volker R. ; Tran, Ngoc Quyen ; Huynh, Khon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c374t-772d63304112438245692795b86fcb948229025dbf291cea0103a4b1e5c1113e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biological effects</topic><topic>Cell adhesion & migration</topic><topic>cell free assembly</topic><topic>Cell migration</topic><topic>Cytology</topic><topic>Dialysis</topic><topic>fibrillar fibronectin</topic><topic>Fibrillogenesis</topic><topic>Fibroblasts</topic><topic>Fibronectin</topic><topic>Fibrous structure</topic><topic>Morphology</topic><topic>Scanning electron microscopy</topic><topic>Urea</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le, Phong</creatorcontrib><creatorcontrib>Mai-Thi, Hoang-Nghi</creatorcontrib><creatorcontrib>Stoldt, Volker R.</creatorcontrib><creatorcontrib>Tran, Ngoc Quyen</creatorcontrib><creatorcontrib>Huynh, Khon</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Le, Phong</au><au>Mai-Thi, Hoang-Nghi</au><au>Stoldt, Volker R.</au><au>Tran, Ngoc Quyen</au><au>Huynh, Khon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphological dependent effect of cell-free formed supramolecular fibronectin on cellular activities</atitle><jtitle>Biological chemistry</jtitle><addtitle>Biol Chem</addtitle><date>2021-01-27</date><risdate>2021</risdate><volume>402</volume><issue>2</issue><spage>155</spage><epage>165</epage><pages>155-165</pages><issn>1431-6730</issn><eissn>1437-4315</eissn><abstract>Fibrillar fibronectin (FFN), an active form of fibronectin (FN), plays important roles in various cellular processes. Our goal is to investigate effect of FFN morphology on cellular behaviors. Plasma FN at two concentrations was cross-linked into FFN by dialysis against 2 M urea followed by morphological analysis under Scanning Electron Microscopy. To evaluate effect of FFN morphology, fibroblasts were cultured on FN or different FFNs. Fibroblast behaviors including adhesion, spreading, and migration were evaluated. Our data showed that FN fibrillogenesis was dependent on FN concentration. At high concentrations (0.75 mg/mL), large FFN approximately 2.167 + 0.875 µm in diameter were formed with attached nodular structures and rough surface. In contrast, smooth surface FFN fibrils with diameter of 1.886 + 0.412 µm were formed from FN at 0.25 mg/mL. Cellular assays revealed morphological dependent biological effects of different FFNs. Fibroblast separately adhered to native FN and remained spherical while on FFN, cells attached with higher quantity and showed spreading morphology. A synergistic ligand interaction of integrin α5β1 and αvβ3 was observed in cell adhering on FFN. Cell migration results showed that large FFN decreased migration rate while small FFN did not. Taken together, our data draws new attention towards controlling biological function of FN by its fibrillar structure.</abstract><cop>Germany</cop><pub>De Gruyter</pub><pmid>33544471</pmid><doi>10.1515/hsz-2019-0402</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-5630-0369</orcidid></addata></record> |
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subjects | Biological effects Cell adhesion & migration cell free assembly Cell migration Cytology Dialysis fibrillar fibronectin Fibrillogenesis Fibroblasts Fibronectin Fibrous structure Morphology Scanning electron microscopy Urea |
title | Morphological dependent effect of cell-free formed supramolecular fibronectin on cellular activities |
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