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Suppression of embryonic lung branching morphogenesis by antisense oligonucleotides against HOM/C homeobox factors
The role of HOM/C homeobox genes on rat embryonic lung branching morphogenesis was investigated using the lung bud explant culture system in an air/liquid interface. Knock down of homeobox b3 and b4 expression by antisense oligonucleotide treatment repressed airway branch formation, while antisense...
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Published in: | In vitro cellular & developmental biology. Animal 2010-09, Vol.46 (8), p.664-672 |
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creator | Yoshimi, Tatsuya Hashimoto, Fumiko Takahashi, Shigeru Takahashi, Yuji |
description | The role of HOM/C homeobox genes on rat embryonic lung branching morphogenesis was investigated using the lung bud explant culture system in an air/liquid interface. Knock down of homeobox b3 and b4 expression by antisense oligonucleotide treatment repressed airway branch formation, while antisense oligonucleotide against homeobox a3 showed no effect. Addition of antisense Hoxb3 oligonucleotide resulted in upregulation of collagen type III mRNA and fibroblast growth factor 10 mRNA, while that of the T-box regulatory factor-4 was decreased. Consequently, expression of Clara cell-specific secretory protein was decreased. These results suggest a critical role for homeobox b3 and b4 genes in lung airway branching morphogenesis. |
doi_str_mv | 10.1007/s11626-010-9322-2 |
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Knock down of homeobox b3 and b4 expression by antisense oligonucleotide treatment repressed airway branch formation, while antisense oligonucleotide against homeobox a3 showed no effect. Addition of antisense Hoxb3 oligonucleotide resulted in upregulation of collagen type III mRNA and fibroblast growth factor 10 mRNA, while that of the T-box regulatory factor-4 was decreased. Consequently, expression of Clara cell-specific secretory protein was decreased. These results suggest a critical role for homeobox b3 and b4 genes in lung airway branching morphogenesis.</description><identifier>ISSN: 1071-2690</identifier><identifier>EISSN: 1543-706X</identifier><identifier>DOI: 10.1007/s11626-010-9322-2</identifier><identifier>PMID: 20535580</identifier><identifier>CODEN: IVCAED</identifier><language>eng</language><publisher>New York: New York : Springer-Verlag</publisher><subject>Animal Genetics and Genomics ; Animals ; Antibodies ; Antisense oligonucleotides ; Biomedical and Life Sciences ; CELL AND TISSUE MODELS ; Cell Biology ; Cell Culture ; Collagen Type III - genetics ; Collagens ; Developmental Biology ; Epithelial cells ; Fibroblast Growth Factor 10 - genetics ; Genes ; Homeobox genes ; Homeodomain Proteins - genetics ; Homeodomain Proteins - physiology ; Life Sciences ; Lung - embryology ; Lung - metabolism ; Lungs ; Messenger RNA ; Morphogenesis ; Oligonucleotides ; Oligonucleotides, Antisense - genetics ; Rats ; Rats, Sprague-Dawley ; Stem Cells ; Up-Regulation</subject><ispartof>In vitro cellular & developmental biology. 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Animal</title><addtitle>In Vitro Cell.Dev.Biol.-Animal</addtitle><addtitle>In Vitro Cell Dev Biol Anim</addtitle><description>The role of HOM/C homeobox genes on rat embryonic lung branching morphogenesis was investigated using the lung bud explant culture system in an air/liquid interface. Knock down of homeobox b3 and b4 expression by antisense oligonucleotide treatment repressed airway branch formation, while antisense oligonucleotide against homeobox a3 showed no effect. Addition of antisense Hoxb3 oligonucleotide resulted in upregulation of collagen type III mRNA and fibroblast growth factor 10 mRNA, while that of the T-box regulatory factor-4 was decreased. Consequently, expression of Clara cell-specific secretory protein was decreased. These results suggest a critical role for homeobox b3 and b4 genes in lung airway branching morphogenesis.</description><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Antisense oligonucleotides</subject><subject>Biomedical and Life Sciences</subject><subject>CELL AND TISSUE MODELS</subject><subject>Cell Biology</subject><subject>Cell Culture</subject><subject>Collagen Type III - genetics</subject><subject>Collagens</subject><subject>Developmental Biology</subject><subject>Epithelial cells</subject><subject>Fibroblast Growth Factor 10 - genetics</subject><subject>Genes</subject><subject>Homeobox genes</subject><subject>Homeodomain Proteins - genetics</subject><subject>Homeodomain Proteins - physiology</subject><subject>Life Sciences</subject><subject>Lung - embryology</subject><subject>Lung - metabolism</subject><subject>Lungs</subject><subject>Messenger RNA</subject><subject>Morphogenesis</subject><subject>Oligonucleotides</subject><subject>Oligonucleotides, Antisense - genetics</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Stem Cells</subject><subject>Up-Regulation</subject><issn>1071-2690</issn><issn>1543-706X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAUhSMEou3AA7AArG5YhV7biX-WaAQUqaiLUomd5Th2xqPEHuxEYt4ej1KKxAK88ZXOd4_lc6rqFYb3GIBfZYwZYTVgqCUlpCZPqnPcNrTmwL4_LTNwXBMm4ay6yHkP5UjMnldnBFratgLOq3S3HA7J5uxjQNEhO3XpGIM3aFzCgLqkg9n5Mk0xHXZxsMFmn1F3RDrMPtuQLYqjH2JYzGjj7HubkR60D3lG17dfr7ZoFycbu_gTOW3mmPKL6pnTY7YvH-5Ndf_p47ftdX1z-_nL9sNNbRqAubYMO2OoM4L2XEqnhXAEgOnesRZzTNri11MuDMXGcYkLInvojBCM99jRTfVu9T2k-GOxeVaTz8aOow42LllJILQlQNl_Sd5IAMFLspvq8i9yH5cUyjcUb9kpVskLhFfIpJhzsk4dkp90OioM6lScWotTpTh1Kk6RsvPmwXjpJts_bvxuqgBkBXKRwmDTn5f_5fp6XdrnkvyjaQOSCMxE0d-uutNR6SH5rO7vCGAKWIi24ZL-AmUot7E</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Yoshimi, Tatsuya</creator><creator>Hashimoto, Fumiko</creator><creator>Takahashi, Shigeru</creator><creator>Takahashi, Yuji</creator><general>New York : Springer-Verlag</general><general>Springer Science + Business Media</general><general>Springer-Verlag</general><general>Society for In Vitro Biology</general><scope>FBQ</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>3V.</scope><scope>4T-</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>7QO</scope><scope>7TM</scope></search><sort><creationdate>20100901</creationdate><title>Suppression of embryonic lung branching morphogenesis by antisense oligonucleotides against HOM/C homeobox factors</title><author>Yoshimi, Tatsuya ; Hashimoto, Fumiko ; Takahashi, Shigeru ; Takahashi, Yuji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-e61fcc3fc83d799fa88f2006adf6517125facd378c31cf7919fa9d0bc8867d1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animal Genetics and Genomics</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Antisense oligonucleotides</topic><topic>Biomedical and Life Sciences</topic><topic>CELL AND TISSUE MODELS</topic><topic>Cell Biology</topic><topic>Cell Culture</topic><topic>Collagen Type III - 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Animal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshimi, Tatsuya</au><au>Hashimoto, Fumiko</au><au>Takahashi, Shigeru</au><au>Takahashi, Yuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suppression of embryonic lung branching morphogenesis by antisense oligonucleotides against HOM/C homeobox factors</atitle><jtitle>In vitro cellular & developmental biology. Animal</jtitle><stitle>In Vitro Cell.Dev.Biol.-Animal</stitle><addtitle>In Vitro Cell Dev Biol Anim</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>46</volume><issue>8</issue><spage>664</spage><epage>672</epage><pages>664-672</pages><issn>1071-2690</issn><eissn>1543-706X</eissn><coden>IVCAED</coden><abstract>The role of HOM/C homeobox genes on rat embryonic lung branching morphogenesis was investigated using the lung bud explant culture system in an air/liquid interface. Knock down of homeobox b3 and b4 expression by antisense oligonucleotide treatment repressed airway branch formation, while antisense oligonucleotide against homeobox a3 showed no effect. Addition of antisense Hoxb3 oligonucleotide resulted in upregulation of collagen type III mRNA and fibroblast growth factor 10 mRNA, while that of the T-box regulatory factor-4 was decreased. Consequently, expression of Clara cell-specific secretory protein was decreased. These results suggest a critical role for homeobox b3 and b4 genes in lung airway branching morphogenesis.</abstract><cop>New York</cop><pub>New York : Springer-Verlag</pub><pmid>20535580</pmid><doi>10.1007/s11626-010-9322-2</doi><tpages>9</tpages></addata></record> |
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subjects | Animal Genetics and Genomics Animals Antibodies Antisense oligonucleotides Biomedical and Life Sciences CELL AND TISSUE MODELS Cell Biology Cell Culture Collagen Type III - genetics Collagens Developmental Biology Epithelial cells Fibroblast Growth Factor 10 - genetics Genes Homeobox genes Homeodomain Proteins - genetics Homeodomain Proteins - physiology Life Sciences Lung - embryology Lung - metabolism Lungs Messenger RNA Morphogenesis Oligonucleotides Oligonucleotides, Antisense - genetics Rats Rats, Sprague-Dawley Stem Cells Up-Regulation |
title | Suppression of embryonic lung branching morphogenesis by antisense oligonucleotides against HOM/C homeobox factors |
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