Literature DB >> 8821033

Differential mRNA regulation of integrin subunits alpha V, beta 1, beta 3, and beta 5 during mouse embryonic organogenesis.

S Yamada1, K E Brown, K M Yamada.   

Abstract

Cell interactions with extracellular matrices play important roles in morphogenetic processes during embryonic development. Extracellular matrix receptors of the integrin family have been implicated in these steps. Recent studies indicate that a variety of integrins can be differentially expressed during development, consistent with diverse roles for integrins in embryogenesis. The present study compares the expression patterns of several major members of the alpha V integrin subfamily, focusing on mRNA expression of alpha V, beta 1, beta 3, and beta 5 subunits during mouse embryonic organogenesis using Northern blot analysis and in situ hybridization. The alpha V and beta 1 subunits showed widespread tissue expression, although most tissues expressed alpha V at relatively low or basal levels. The mRNA for beta 5 was also expressed in a variety of embryonic organs and showed unusual localization patterns in certain organs. Striking, high-level expression of beta 5 transcripts was detected in the ependymal layer of the central nervous system, glomeruli of the kidney, epicardial region of the heart, and in the tooth germs, suggesting specific functions for this molecule during morphogenetic events in these organs. In contrast, few beta 3 transcripts were expressed during mid-gestation mouse embryogenesis except in megakaryocytes within the embryonic liver. These observations of differing expression spectra suggest that members of the alpha V integrin subfamily have distinct roles and also suggests that they have different transcriptional regulation. The beta 5 integrin is unique in its degree of tissue-specific mRNA regulation associated with morphogenesis of embryonic organs.

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Year:  1995        PMID: 8821033     DOI: 10.3109/15419069509081016

Source DB:  PubMed          Journal:  Cell Adhes Commun        ISSN: 1023-7046


  8 in total

1.  Cross talk between beta(1) and alpha(V) integrins: beta(1) affects beta(3) mRNA stability.

Authors:  S F Retta; G Cassarà; M D'Amato; R Alessandro; M Pellegrino; S Degani; G De Leo; L Silengo; G Tarone
Journal:  Mol Biol Cell       Date:  2001-10       Impact factor: 4.138

2.  Coordinated regulation and colocalization of alphav integrin and its activating enzyme proprotein convertase PC5 in vivo.

Authors:  Philipp Stawowy; Kristof Graf; Stephan Goetze; Mattias Roser; Michel Chrétien; Nabil G Seidah; Eckart Fleck; Mieczyslaw Marcinkiewicz
Journal:  Histochem Cell Biol       Date:  2003-02-20       Impact factor: 4.304

3.  Integrin alphaV is necessary for gastrulation movements that regulate vertebrate body asymmetry.

Authors:  Ararat J Ablooglu; Eugene Tkachenko; Jian Kang; Sanford J Shattil
Journal:  Development       Date:  2010-09-15       Impact factor: 6.868

4.  Cooperation between VEGF and beta3 integrin during cardiac vascular development.

Authors:  Sara M Weis; Jeffrey N Lindquist; Leo A Barnes; Kimberly M Lutu-Fuga; Jianhua Cui; Malcolm R Wood; David A Cheresh
Journal:  Blood       Date:  2006-10-24       Impact factor: 22.113

5.  cDNA cloning reveals two mouse beta5 integrin transcripts distinct in cytoplasmic domains as a result of alternative splicing.

Authors:  H Zhang; S M Tan; J Lu
Journal:  Biochem J       Date:  1998-04-15       Impact factor: 3.857

6.  A simple technique to establish a long-term adenovirus mediated gene transfer to the heart of newborn mice.

Authors:  Marina Jerebtsova; Xuehai Ye; Patricio E Ray
Journal:  Cardiovasc Hematol Disord Drug Targets       Date:  2009-06

7.  Lentviral-mediated RNAi to inhibit target gene expression of the porcine integrin αv subunit, the FMDV receptor, and against FMDV infection in PK-15 cells.

Authors:  Jihuai Luo; Junzheng Du; Shandian Gao; Guofeng Zhang; Jingjing Sun; Guozheng Cong; Junjun Shao; Tong Lin; Huiyun Chang
Journal:  Virol J       Date:  2011-09-07       Impact factor: 4.099

8.  Deletion of exon 20 of the Familial Dysautonomia gene Ikbkap in mice causes developmental delay, cardiovascular defects, and early embryonic lethality.

Authors:  Paula Dietrich; Junming Yue; Shuyu E; Ioannis Dragatsis
Journal:  PLoS One       Date:  2011-10-28       Impact factor: 3.240

  8 in total

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