Home LiteratureArticle Details
PMID: 8143928 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Expression of transforming growth factor-beta 2 and beta 3 mRNAs and proteins in the developing chicken embryo.

Differentiation; research in biological diversity ·Vol. 55 ·No. 2 ·1994-01-00 ·Pages 105-18

Jakowlew SB, Ciment G, Tuan RS, Sporn MB, Roberts AB

Abstract

Specific cDNA probes and antibodies for chicken transforming growth factor (TGF)-beta 2 and beta 3 were used to study expression of TGF-beta 2 and beta 3 mRNAs and proteins in the developing chicken embryo. Expression of the mRNAs for both TGF-beta isoforms was detected by day 1.5 of incubation (Hamburger and Hamilton stage 10) by RNA Northern blot analysis and increased with developmental age. Expression of TGF-beta 2 and beta 3 mRNAs was detected in every embryonic tissue examined, with the level of expression of both isoforms being high in heart, brain and muscle and low in kidney and liver. Coordinate unidirectional upregulation of expression of TGF-beta 2 and beta 3 mRNAs occurred in most embryonic tissues with development except the heart, where the steady-state level of expression of TGF-beta 2 mRNA decreased with age, while that of TGF-beta 3 mRNA increased. In situ hybridization analysis detected TGF-beta 2 and beta 3 mRNAs as early as the definitive primitive streak stage (stage 4). During neurulation (stage 10), TGF-beta 2 and beta 3 mRNAs were detected in cells of all three germ layers; TGF-beta 3 mRNA was detected in neurectoderm as well. Following neurulation, TGF-beta 3 mRNA was detected in the neural tube, notochord, ectoderm, endoderm, sclerotome and dermomyotome at stage 16; expression of TGF-beta 2 mRNA was not as prominent as TGF-beta 3 mRNA in these structures. By stage 29, both TGF-beta 2 and beta 3 mRNAs were localized in several tissues including heart, lung, gizzard and feathers. Immunohistochemical staining analysis detected immunoreactive TGF-beta 2 and beta 3 proteins in all three germ layers of stage 4 embryos. Staining for TGF-beta 2 and beta 3 proteins was detected in several cell types and tissues in the early developing embryo frequently in the same locations as TGF-beta 2 and beta 3 mRNAs, with staining for TGF-beta 2 being less intense than TGF-beta 3. However, in some cases, localization of TGF-beta 2 and beta 3 proteins was different from that of the mRNAs, indicating that a complex mechanism of transcription, translation and secretion exits during chicken embryogenesis. These and other results suggest that TGF-beta 2 and beta 3 may play important roles and act through both autocrine and paracrine mechanisms in the development of many tissues in the chicken.

MeSH Terms
Animals Antibodies Blotting, Northern Chick Embryo/cytology,physiology DNA Probes Embryonic and Fetal Development Gene Expression Immunohistochemistry In Situ Hybridization RNA, Messenger/analysis,biosynthesis Time Factors Transforming Growth Factor beta/analysis,biosynthesis
Chemicals
Antibodies DNA Probes RNA, Messenger Transforming Growth Factor beta
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Jakowlew S B
National Cancer Institute, Laboratory of Chemoprevention, Bethesda, Maryland 20892.
Ciment G
Tuan R S
Sporn M B
Roberts A B
Article Info
Journal
Differentiation; research in biological diversity
Abbr.
Differentiation
ISSN
0301-4681
Published
1994-01-00
Pages
105-18
Language
English
Region
England
NLM ID
0401650
Subset
IM
Grants
NICHD NIH HHS · HD 15822 · United States
NICHD NIH HHS · HD 29937 · United States
NINDS NIH HHS · NS 23883 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com