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Different Substrates Influence the Expression of Intermediate Filaments and the Deposition of Basement Membrane Proteins
A primary culture of serous cystadenocarcinoma of the ovary was used to study the expression of intermediate filament proteins and the deposition of basal lamina proteins. It was found that cells grown on type I and IV collagens or in collagen gels failed to express vimentin, which was readily demon...
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Published in: | In Vitro Cellular & Developmental Biology 1988-03, Vol.24 (3), p.183-187 |
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creator | Liscia, Daniel S. Amelia Bernardi Bona Griselli Alberto P. M. Cappa |
description | A primary culture of serous cystadenocarcinoma of the ovary was used to study the expression of intermediate filament proteins and the deposition of basal lamina proteins. It was found that cells grown on type I and IV collagens or in collagen gels failed to express vimentin, which was readily demonstrable in cultures of the same cells grown on plastic or glass. Furthermore cells grown in collagen gels formed colonics demonstrating a cystic architecture. Unlike what is commonly observed on glass or plastic, where laminin and fibronectin are deposited as disorganized fibrils in the extracellular space, in or on collagen these proteins appear solely at the interface between the epithelial cells and matrix. The results suggest that the extracellular matrix influences the cytoskeletal organization of the intermediate filaments and determines cell polarity. They confirm that collagen substrates permit epithelial cell cultures to progress toward a more differentiated state. |
doi_str_mv | 10.1007/bf02623544 |
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M. Cappa</creator><creatorcontrib>Liscia, Daniel S. ; Amelia Bernardi ; Bona Griselli ; Alberto P. M. Cappa</creatorcontrib><description>A primary culture of serous cystadenocarcinoma of the ovary was used to study the expression of intermediate filament proteins and the deposition of basal lamina proteins. It was found that cells grown on type I and IV collagens or in collagen gels failed to express vimentin, which was readily demonstrable in cultures of the same cells grown on plastic or glass. Furthermore cells grown in collagen gels formed colonics demonstrating a cystic architecture. Unlike what is commonly observed on glass or plastic, where laminin and fibronectin are deposited as disorganized fibrils in the extracellular space, in or on collagen these proteins appear solely at the interface between the epithelial cells and matrix. The results suggest that the extracellular matrix influences the cytoskeletal organization of the intermediate filaments and determines cell polarity. They confirm that collagen substrates permit epithelial cell cultures to progress toward a more differentiated state.</description><identifier>ISSN: 0883-8364</identifier><identifier>EISSN: 2327-431X</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/bf02623544</identifier><identifier>PMID: 2450860</identifier><identifier>CODEN: ICDBEO</identifier><language>eng</language><publisher>Largo, MD: Tissue Culture Association, Inc</publisher><subject>Animal cells ; Basement Membrane - metabolism ; Biological and medical sciences ; Biotechnology ; Cell Count ; Cell culture techniques ; Cell cultures. Hybridization. Fusion ; Cell Division ; Cell growth ; Cell lines ; Collagen ; Collagens ; Cultured cells ; Cystadenocarcinoma ; Cystadenocarcinoma - metabolism ; Cystadenocarcinoma - ultrastructure ; Cytoskeleton - ultrastructure ; Epithelial cells ; Epithelium - metabolism ; Epithelium - ultrastructure ; Establishment of new cell lines, improvement of cultural methods, mass cultures ; Eukaryotic cell cultures ; Extracellular Matrix - metabolism ; Female ; Fibronectins - biosynthesis ; Fundamental and applied biological sciences. Psychology ; Gels ; Humans ; Intermediate Filament Proteins - biosynthesis ; Intermediate filaments ; Intermediate Filaments - metabolism ; Intermediate Filaments - ultrastructure ; Keratins - biosynthesis ; Laminin - biosynthesis ; Membrane Proteins - metabolism ; Methods. Procedures. 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M. Cappa</creatorcontrib><title>Different Substrates Influence the Expression of Intermediate Filaments and the Deposition of Basement Membrane Proteins</title><title>In Vitro Cellular & Developmental Biology</title><addtitle>In Vitro Cell Dev Biol</addtitle><description>A primary culture of serous cystadenocarcinoma of the ovary was used to study the expression of intermediate filament proteins and the deposition of basal lamina proteins. It was found that cells grown on type I and IV collagens or in collagen gels failed to express vimentin, which was readily demonstrable in cultures of the same cells grown on plastic or glass. Furthermore cells grown in collagen gels formed colonics demonstrating a cystic architecture. Unlike what is commonly observed on glass or plastic, where laminin and fibronectin are deposited as disorganized fibrils in the extracellular space, in or on collagen these proteins appear solely at the interface between the epithelial cells and matrix. The results suggest that the extracellular matrix influences the cytoskeletal organization of the intermediate filaments and determines cell polarity. They confirm that collagen substrates permit epithelial cell cultures to progress toward a more differentiated state.</description><subject>Animal cells</subject><subject>Basement Membrane - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell Count</subject><subject>Cell culture techniques</subject><subject>Cell cultures. Hybridization. Fusion</subject><subject>Cell Division</subject><subject>Cell growth</subject><subject>Cell lines</subject><subject>Collagen</subject><subject>Collagens</subject><subject>Cultured cells</subject><subject>Cystadenocarcinoma</subject><subject>Cystadenocarcinoma - metabolism</subject><subject>Cystadenocarcinoma - ultrastructure</subject><subject>Cytoskeleton - ultrastructure</subject><subject>Epithelial cells</subject><subject>Epithelium - metabolism</subject><subject>Epithelium - ultrastructure</subject><subject>Establishment of new cell lines, improvement of cultural methods, mass cultures</subject><subject>Eukaryotic cell cultures</subject><subject>Extracellular Matrix - metabolism</subject><subject>Female</subject><subject>Fibronectins - biosynthesis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gels</subject><subject>Humans</subject><subject>Intermediate Filament Proteins - biosynthesis</subject><subject>Intermediate filaments</subject><subject>Intermediate Filaments - metabolism</subject><subject>Intermediate Filaments - ultrastructure</subject><subject>Keratins - biosynthesis</subject><subject>Laminin - biosynthesis</subject><subject>Membrane Proteins - metabolism</subject><subject>Methods. Procedures. Technologies</subject><subject>Middle Aged</subject><subject>Molecular and cellular biology</subject><subject>Ovarian Neoplasms - metabolism</subject><subject>Ovarian Neoplasms - ultrastructure</subject><subject>Space life sciences</subject><subject>Tumor Cells, Cultured</subject><subject>Vimentin</subject><subject>Vimentin - biosynthesis</subject><issn>0883-8364</issn><issn>2327-431X</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNo9kE1r3DAQhkVoSbdpLj23oEPpoeBGX5bsY_OxSSAhhSSQm5HlEVXwx0YjQ_Lvq-26e5rD88zLzEvIZ85-csbMSeuZ0EKWSh2QlZDCFEryp3dkxapKFpXU6gP5iPjMmGRaiENyKFTJKs1W5PU8eA8RxkTv5xZTtAmQXo--n2F0QNMfoBevmwiIYRrp5DNLEAfoQjbpOvR2yMtI7dj9k89hM2FIi3xqEbac3sLQRjsC_R2nBGHET-S9tz3C8TKPyOP64uHsqri5u7w--3VTOClFKpQyzonO8LbS1ihddtIpJoArY5hn2ney6zpRCuYE01bLsjbcgpKmzGvA5BH5vsvdxOllBkzNENBB3-djphkbU3FZyZJn8cdOdHFCjOCbTQyDjW8NZ8225uZ0_b_mLH9dUuc2d7FXl14z_7Zwi872Pr_uAu41XddVXW9jvuy0Z0xT3GMlas3rUv4Fu-WOmw</recordid><startdate>19880301</startdate><enddate>19880301</enddate><creator>Liscia, Daniel S.</creator><creator>Amelia Bernardi</creator><creator>Bona Griselli</creator><creator>Alberto P. M. Cappa</creator><general>Tissue Culture Association, Inc</general><general>Society for In Vitro Biology</general><scope>IQODW</scope><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></search><sort><creationdate>19880301</creationdate><title>Different Substrates Influence the Expression of Intermediate Filaments and the Deposition of Basement Membrane Proteins</title><author>Liscia, Daniel S. ; Amelia Bernardi ; Bona Griselli ; Alberto P. M. Cappa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-447cc2d71b86a7465d3c402e14770f06fd3ddd2520c206a635971ae4375c2de03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Animal cells</topic><topic>Basement Membrane - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell Count</topic><topic>Cell culture techniques</topic><topic>Cell cultures. Hybridization. Fusion</topic><topic>Cell Division</topic><topic>Cell growth</topic><topic>Cell lines</topic><topic>Collagen</topic><topic>Collagens</topic><topic>Cultured cells</topic><topic>Cystadenocarcinoma</topic><topic>Cystadenocarcinoma - metabolism</topic><topic>Cystadenocarcinoma - ultrastructure</topic><topic>Cytoskeleton - ultrastructure</topic><topic>Epithelial cells</topic><topic>Epithelium - metabolism</topic><topic>Epithelium - ultrastructure</topic><topic>Establishment of new cell lines, improvement of cultural methods, mass cultures</topic><topic>Eukaryotic cell cultures</topic><topic>Extracellular Matrix - metabolism</topic><topic>Female</topic><topic>Fibronectins - biosynthesis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gels</topic><topic>Humans</topic><topic>Intermediate Filament Proteins - biosynthesis</topic><topic>Intermediate filaments</topic><topic>Intermediate Filaments - metabolism</topic><topic>Intermediate Filaments - ultrastructure</topic><topic>Keratins - biosynthesis</topic><topic>Laminin - biosynthesis</topic><topic>Membrane Proteins - metabolism</topic><topic>Methods. Procedures. Technologies</topic><topic>Middle Aged</topic><topic>Molecular and cellular biology</topic><topic>Ovarian Neoplasms - metabolism</topic><topic>Ovarian Neoplasms - ultrastructure</topic><topic>Space life sciences</topic><topic>Tumor Cells, Cultured</topic><topic>Vimentin</topic><topic>Vimentin - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liscia, Daniel S.</creatorcontrib><creatorcontrib>Amelia Bernardi</creatorcontrib><creatorcontrib>Bona Griselli</creatorcontrib><creatorcontrib>Alberto P. M. 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Cappa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Different Substrates Influence the Expression of Intermediate Filaments and the Deposition of Basement Membrane Proteins</atitle><jtitle>In Vitro Cellular & Developmental Biology</jtitle><addtitle>In Vitro Cell Dev Biol</addtitle><date>1988-03-01</date><risdate>1988</risdate><volume>24</volume><issue>3</issue><spage>183</spage><epage>187</epage><pages>183-187</pages><issn>0883-8364</issn><eissn>2327-431X</eissn><eissn>1475-2689</eissn><coden>ICDBEO</coden><abstract>A primary culture of serous cystadenocarcinoma of the ovary was used to study the expression of intermediate filament proteins and the deposition of basal lamina proteins. It was found that cells grown on type I and IV collagens or in collagen gels failed to express vimentin, which was readily demonstrable in cultures of the same cells grown on plastic or glass. Furthermore cells grown in collagen gels formed colonics demonstrating a cystic architecture. Unlike what is commonly observed on glass or plastic, where laminin and fibronectin are deposited as disorganized fibrils in the extracellular space, in or on collagen these proteins appear solely at the interface between the epithelial cells and matrix. The results suggest that the extracellular matrix influences the cytoskeletal organization of the intermediate filaments and determines cell polarity. They confirm that collagen substrates permit epithelial cell cultures to progress toward a more differentiated state.</abstract><cop>Largo, MD</cop><pub>Tissue Culture Association, Inc</pub><pmid>2450860</pmid><doi>10.1007/bf02623544</doi><tpages>5</tpages></addata></record> |
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subjects | Animal cells Basement Membrane - metabolism Biological and medical sciences Biotechnology Cell Count Cell culture techniques Cell cultures. Hybridization. Fusion Cell Division Cell growth Cell lines Collagen Collagens Cultured cells Cystadenocarcinoma Cystadenocarcinoma - metabolism Cystadenocarcinoma - ultrastructure Cytoskeleton - ultrastructure Epithelial cells Epithelium - metabolism Epithelium - ultrastructure Establishment of new cell lines, improvement of cultural methods, mass cultures Eukaryotic cell cultures Extracellular Matrix - metabolism Female Fibronectins - biosynthesis Fundamental and applied biological sciences. Psychology Gels Humans Intermediate Filament Proteins - biosynthesis Intermediate filaments Intermediate Filaments - metabolism Intermediate Filaments - ultrastructure Keratins - biosynthesis Laminin - biosynthesis Membrane Proteins - metabolism Methods. Procedures. Technologies Middle Aged Molecular and cellular biology Ovarian Neoplasms - metabolism Ovarian Neoplasms - ultrastructure Space life sciences Tumor Cells, Cultured Vimentin Vimentin - biosynthesis |
title | Different Substrates Influence the Expression of Intermediate Filaments and the Deposition of Basement Membrane Proteins |
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