Mice lacking the EDB segment of fibronectin develop normally but exhibit reduced cell growth and fibronectin matrix assembly in vitro

Fibronectins (FNs) are major cell-adhesive proteins in the extracellular matrix and are essential for embryonic development. FNs are encoded by a single gene, but heterogeneity is introduced by alternative pre-mRNA splicing. One of the alternatively spliced segments, extra domain B (EDB), is promine...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2002-10, Vol.62 (19), p.5603-5610
Hauptverfasser: FUKUDA, Tomohiko, YOSHIDA, Nobuaki, KATAOKA, Yuki, MANABE, Ri-Ichiroh, MIZUNO-HORIKAWA, Yoko, SATO, Motohiko, KURIYAMA, Kohji, YASUI, Natsuo, SEKIGUCHI, Kiyotoshi
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container_issue 19
container_start_page 5603
container_title Cancer research (Chicago, Ill.)
container_volume 62
creator FUKUDA, Tomohiko
YOSHIDA, Nobuaki
KATAOKA, Yuki
MANABE, Ri-Ichiroh
MIZUNO-HORIKAWA, Yoko
SATO, Motohiko
KURIYAMA, Kohji
YASUI, Natsuo
SEKIGUCHI, Kiyotoshi
description Fibronectins (FNs) are major cell-adhesive proteins in the extracellular matrix and are essential for embryonic development. FNs are encoded by a single gene, but heterogeneity is introduced by alternative pre-mRNA splicing. One of the alternatively spliced segments, extra domain B (EDB), is prominently expressed during embryonic development and in tumor tissues, although it is mostly eliminated from FN in normal adult tissues. To examine the function of the EDB segment in vivo, we generated mice lacking the EDB exon using the Cre-loxP system. Although EDB-containing FNs are highly expressed throughout early embryogenesis, EDB-deficient mice developed normally and were fertile. Despite the absence of any significant phenotypes observed in vivo, however, fibroblasts obtained from EDB-deficient mice grew slowly in vitro and deposited less FN in the pericellular matrix than fibroblasts from wild-type mice. These results indicate that expression of EDB-containing isoforms is dispensable during embryonic development, yet may play a modulating role in the growth of connective tissue cells via the FN matrix.
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FNs are encoded by a single gene, but heterogeneity is introduced by alternative pre-mRNA splicing. One of the alternatively spliced segments, extra domain B (EDB), is prominently expressed during embryonic development and in tumor tissues, although it is mostly eliminated from FN in normal adult tissues. To examine the function of the EDB segment in vivo, we generated mice lacking the EDB exon using the Cre-loxP system. Although EDB-containing FNs are highly expressed throughout early embryogenesis, EDB-deficient mice developed normally and were fertile. Despite the absence of any significant phenotypes observed in vivo, however, fibroblasts obtained from EDB-deficient mice grew slowly in vitro and deposited less FN in the pericellular matrix than fibroblasts from wild-type mice. 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Psychology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Molecular and cellular biology</subject><subject>Molecular Sequence Data</subject><subject>Protein Isoforms</subject><subject>Protein Structure, Tertiary - genetics</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpV0M1OwzAMB_AKgdgYvALKBW6VmiZp2iOM8SENcYFzlaTOGmiTkaRjewDemyKGECfL1s9_WT5IppiRMuWUssNkmmVZmTLK80lyEsLr2DKcseNkgnPCKs7pNPl8NApQJ9SbsSsUW0CLm2sUYNWDjchppI30zoKKxqIGNtC5NbLO96LrdkgOEcG2NdJE5KEZFDRIQdehlXcfsUXCNv8CehG92SIRAvRy3B9HGxO9O02OtOgCnO3rLHm5XTzP79Pl093D_GqZtjnHMZWUMK4ayjAFCRLrjKs8V0rKqlAFxUwQXZZMKahopYXmoilwQatGc5wRSsksufzJXXv3PkCIdW_C98HCghtCzXNMcV6SEZ7v4SB7aOq1N73wu_r3cSO42AMRlOi0F1aZ8OdIxQghjHwB96p6Mw</recordid><startdate>20021001</startdate><enddate>20021001</enddate><creator>FUKUDA, Tomohiko</creator><creator>YOSHIDA, Nobuaki</creator><creator>KATAOKA, Yuki</creator><creator>MANABE, Ri-Ichiroh</creator><creator>MIZUNO-HORIKAWA, Yoko</creator><creator>SATO, Motohiko</creator><creator>KURIYAMA, Kohji</creator><creator>YASUI, Natsuo</creator><creator>SEKIGUCHI, Kiyotoshi</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20021001</creationdate><title>Mice lacking the EDB segment of fibronectin develop normally but exhibit reduced cell growth and fibronectin matrix assembly in vitro</title><author>FUKUDA, Tomohiko ; YOSHIDA, Nobuaki ; KATAOKA, Yuki ; MANABE, Ri-Ichiroh ; MIZUNO-HORIKAWA, Yoko ; SATO, Motohiko ; KURIYAMA, Kohji ; YASUI, Natsuo ; SEKIGUCHI, Kiyotoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h271t-b4357cd4514ebeb1f07c22ccbb96c6415a3f885cce949faf7ad61649df7103443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cartilage - growth &amp; development</topic><topic>Cell cycle, cell proliferation</topic><topic>Cell differentiation, maturation, development, hematopoiesis</topic><topic>Cell Division - physiology</topic><topic>Cell physiology</topic><topic>Chimera</topic><topic>Extracellular Matrix - genetics</topic><topic>Extracellular Matrix - metabolism</topic><topic>Extracellular Matrix - physiology</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - metabolism</topic><topic>Fibronectins - genetics</topic><topic>Fibronectins - metabolism</topic><topic>Fibronectins - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Molecular and cellular biology</topic><topic>Molecular Sequence Data</topic><topic>Protein Isoforms</topic><topic>Protein Structure, Tertiary - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FUKUDA, Tomohiko</creatorcontrib><creatorcontrib>YOSHIDA, Nobuaki</creatorcontrib><creatorcontrib>KATAOKA, Yuki</creatorcontrib><creatorcontrib>MANABE, Ri-Ichiroh</creatorcontrib><creatorcontrib>MIZUNO-HORIKAWA, Yoko</creatorcontrib><creatorcontrib>SATO, Motohiko</creatorcontrib><creatorcontrib>KURIYAMA, Kohji</creatorcontrib><creatorcontrib>YASUI, Natsuo</creatorcontrib><creatorcontrib>SEKIGUCHI, Kiyotoshi</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FUKUDA, Tomohiko</au><au>YOSHIDA, Nobuaki</au><au>KATAOKA, Yuki</au><au>MANABE, Ri-Ichiroh</au><au>MIZUNO-HORIKAWA, Yoko</au><au>SATO, Motohiko</au><au>KURIYAMA, Kohji</au><au>YASUI, Natsuo</au><au>SEKIGUCHI, Kiyotoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mice lacking the EDB segment of fibronectin develop normally but exhibit reduced cell growth and fibronectin matrix assembly in vitro</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>2002-10-01</date><risdate>2002</risdate><volume>62</volume><issue>19</issue><spage>5603</spage><epage>5610</epage><pages>5603-5610</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Fibronectins (FNs) are major cell-adhesive proteins in the extracellular matrix and are essential for embryonic development. 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source MEDLINE; American Association for Cancer Research; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Amino Acid Sequence
Animals
Biological and medical sciences
Cartilage - growth & development
Cell cycle, cell proliferation
Cell differentiation, maturation, development, hematopoiesis
Cell Division - physiology
Cell physiology
Chimera
Extracellular Matrix - genetics
Extracellular Matrix - metabolism
Extracellular Matrix - physiology
Fibroblasts - cytology
Fibroblasts - metabolism
Fibronectins - genetics
Fibronectins - metabolism
Fibronectins - physiology
Fundamental and applied biological sciences. Psychology
Male
Mice
Mice, Inbred C57BL
Molecular and cellular biology
Molecular Sequence Data
Protein Isoforms
Protein Structure, Tertiary - genetics
title Mice lacking the EDB segment of fibronectin develop normally but exhibit reduced cell growth and fibronectin matrix assembly in vitro
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