Literature DB >> 7821227

Expression of activin subunits, activin receptors and follistatin in postimplantation mouse embryos suggests specific developmental functions for different activins.

A Feijen1, M J Goumans, A J van den Eijnden-van Raaij.   

Abstract

Using in situ hybridization we have studied the localization of the messenger RNAs encoding the inhibin/activin subunits (alpha, beta A, beta B), the activin-binding protein follistatin and activin receptors (IIA, IIB) in mouse embryos during postimplantation development. From 6.5- to 9.5-days post coitum (p.c.) activin beta A and beta B subunit expression was restricted to the decidua, while activin receptor type IIB messages were exclusively detected in the embryo. Expression of activin receptor type IIA was apparent in the embryo as early as 9.5 days p.c. In contrast, follistatin transcripts were present in both the decidua and the embryo at the early postimplantation stages. In particular, the primitive streak region, specific rhombomeres in the developing hindbrain, somites, paraxial mesoderm and parietal endoderm cells attached to the Reichert's membrane showed strong expression of follistatin. In 10.5- and 12.5-day embryos expression of the beta A subunit message was abundant in mesenchymal tissue, in particular in the developing face, the body wall, the heart, precartilage condensations in the limb and in the mesenchyme of structures that show both epithelial and mesenchymal components, including tissues of the embryonic digestive, respiratory and genital tracts. The distribution of beta B transcripts was quite different from that observed for beta A. beta B is strongly expressed in selected regions of the brain, in particular the fore- and hindbrain, and in the spinal cord. Specific hybridization signals were also present in the epithelium of the stomach and oesophagus. Common sites of beta A and beta B expression are blood vessels, intervertebral disc anlagen, mesenchymal condensations in the flank region and the gonad primordium. The latter organ is the only site in the embryo where the alpha subunit is expressed, and thus where inhibit activity may be present. During the period of organogenesis the sites of expression of activin receptors type IIA and IIB messenger RNA (mRNA) generally coincide with or are adjacent to the sites of beta subunit expression. Differences in the expression patterns of the receptor RNAs are the whisker follicles, where type IIA is expressed, and the metanephros and the forebrain where type IIB transcripts are present. Taken together, the present data suggest that follistatin, but not one of the known activin forms (A,B,AB) is involved in early postimplantation development.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7821227     DOI: 10.1242/dev.120.12.3621

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  62 in total

1.  Activin receptor patterning of foregut organogenesis.

Authors:  S K Kim; M Hebrok; E Li; S P Oh; H Schrewe; E B Harmon; J S Lee; D A Melton
Journal:  Genes Dev       Date:  2000-08-01       Impact factor: 11.361

2.  BF-1 interferes with transforming growth factor beta signaling by associating with Smad partners.

Authors:  C Dou; J Lee; B Liu; F Liu; J Massague; S Xuan; E Lai
Journal:  Mol Cell Biol       Date:  2000-09       Impact factor: 4.272

3.  Bmp4 is required for the generation of primordial germ cells in the mouse embryo.

Authors:  K A Lawson; N R Dunn; B A Roelen; L M Zeinstra; A M Davis; C V Wright; J P Korving; B L Hogan
Journal:  Genes Dev       Date:  1999-02-15       Impact factor: 11.361

4.  Activin IIB receptor blockade attenuates dystrophic pathology in a mouse model of Duchenne muscular dystrophy.

Authors:  Kevin J Morine; Lawrence T Bish; Joshua T Selsby; Jeffery A Gazzara; Klara Pendrak; Meg M Sleeper; Elisabeth R Barton; Se-Jin Lee; H Lee Sweeney
Journal:  Muscle Nerve       Date:  2010-11       Impact factor: 3.217

5.  Spatial dynamics of multistage cell lineages in tissue stratification.

Authors:  Ching-Shan Chou; Wing-Cheong Lo; Kimberly K Gokoffski; Yong-Tao Zhang; Frederic Y M Wan; Arthur D Lander; Anne L Calof; Qing Nie
Journal:  Biophys J       Date:  2010-11-17       Impact factor: 4.033

Review 6.  On the origin of the beta cell.

Authors:  Jennifer M Oliver-Krasinski; Doris A Stoffers
Journal:  Genes Dev       Date:  2008-08-01       Impact factor: 11.361

7.  Activin is an essential early mesenchymal signal in tooth development that is required for patterning of the murine dentition.

Authors:  C A Ferguson; A S Tucker; L Christensen; A L Lau; M M Matzuk; P T Sharpe
Journal:  Genes Dev       Date:  1998-08-15       Impact factor: 11.361

8.  The fibroblast integrin alpha11beta1 is induced in a mechanosensitive manner involving activin A and regulates myofibroblast differentiation.

Authors:  Sergio Carracedo; Ning Lu; Svetlana N Popova; Roland Jonsson; Beate Eckes; Donald Gullberg
Journal:  J Biol Chem       Date:  2010-02-02       Impact factor: 5.157

9.  Control of liver cell fate decision by a gradient of TGF beta signaling modulated by Onecut transcription factors.

Authors:  Frédéric Clotman; Patrick Jacquemin; Nicolas Plumb-Rudewiez; Christophe E Pierreux; Patrick Van der Smissen; Harry C Dietz; Pierre J Courtoy; Guy G Rousseau; Frédéric P Lemaigre
Journal:  Genes Dev       Date:  2005-08-15       Impact factor: 11.361

10.  Changes in the reproductive function and developmental phenotypes in mice following intramuscular injection of an activin betaA-expressing plasmid.

Authors:  Mi-Nyeu Kim; Moon Nyeo Park; Hoi Kyung Jung; Chunghee Cho; Kelly E Mayo; Byung-Nam Cho
Journal:  Reprod Biol Endocrinol       Date:  2008-12-16       Impact factor: 5.211

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