Role of transforming growth factor-β in chondrogenic pattern formation in the embryonic limb: Stimulation of mesenchymal condensation and fibronectin gene expression by exogenenous TGF-β and evidence for endogenous TGF-β-like activity

Claire M. Leonard, Howard M. Fuld, Dorothy A. Frenz, Sherry A. Downie, Joan Massague, Stuart A. Newman

Research output: Contribution to journalArticle

186 Citations (Scopus)

Abstract

The possible role of TGF-β-like molecules in skeletal pattern formation in the embryonic vertebrate limb was studied by analyzing the mechanism of enhancement of chondrogenesis in chick wing bud mesenchyme in vitro and testing for the presence and distribution of endogenous TGF-β-like activity in this tissue. Transient exposure (3-6 hr) to TGF-β1 (1-2 ng/ml) on the day after plating resulted in a 1.5- to 2-fold enhancement of accumulation of Alcian blue (pH 1.0)-stainable extracellular matrix 5 days later. The enhancement of differentiation was preceded by an acceleration and an increase in the extent of precartilage condensation formation, visualized by Hoffman Modulation Contrast microscopy a day after TGF-β treatment. In contrast, neither condensation nor subsequent chondrogenesis was stimulated by transient treatment with TGF-β1 on the day of plating. The effectiveness of a TGF-β treatment regimen in enhancing chondrogenesis was correlated with its effectiveness in stimulating condensation formation. Exposures to the factor for 3-6 hr on the day after plating, which most consistently stimulated both condensation formation and chondrogenesis, also corresponded to a peak in the enhancement of the steady-state level of fibronectin mRNA (fourfold to eightfold over control levels) measured at the end of the treatment period. The elevation in fibronectin mRNA levels brought about by this treatment persisted throughout the period of condensation. Endogenous TGF-β-like activity was detected in limb mesenchyme: extracts of freshly isolated and cultured limb tissues contained 6-25 pg TGF-β-like activity per 1 × 106 cells by the Mv1Lu cell proliferation inhibition assay, and indirect immunofluorescence using a polyclonal antibody directed against a TGF-β-related peptide indicated a patchy distribution of endogenous TGF-β-like reactivity within a day after culture. These findings are discussed in relation to the "fibronectin prepattern" hypothesis for limb pattern formation.

Original languageEnglish (US)
Pages (from-to)99-109
Number of pages11
JournalDevelopmental Biology
Volume145
Issue number1
DOIs
StatePublished - 1991

Fingerprint

Body Patterning
Transforming Growth Factors
Chondrogenesis
Fibronectins
Extremities
Gene Expression
Mesoderm
Therapeutics
Alcian Blue
Messenger RNA
Indirect Fluorescent Antibody Technique
Extracellular Matrix
Vertebrates
Microscopy
Cell Proliferation
Peptides
Antibodies

ASJC Scopus subject areas

  • Developmental Biology

Cite this

@article{bc9c8bc086dc4c098a6232b6f36e4910,
title = "Role of transforming growth factor-β in chondrogenic pattern formation in the embryonic limb: Stimulation of mesenchymal condensation and fibronectin gene expression by exogenenous TGF-β and evidence for endogenous TGF-β-like activity",
abstract = "The possible role of TGF-β-like molecules in skeletal pattern formation in the embryonic vertebrate limb was studied by analyzing the mechanism of enhancement of chondrogenesis in chick wing bud mesenchyme in vitro and testing for the presence and distribution of endogenous TGF-β-like activity in this tissue. Transient exposure (3-6 hr) to TGF-β1 (1-2 ng/ml) on the day after plating resulted in a 1.5- to 2-fold enhancement of accumulation of Alcian blue (pH 1.0)-stainable extracellular matrix 5 days later. The enhancement of differentiation was preceded by an acceleration and an increase in the extent of precartilage condensation formation, visualized by Hoffman Modulation Contrast microscopy a day after TGF-β treatment. In contrast, neither condensation nor subsequent chondrogenesis was stimulated by transient treatment with TGF-β1 on the day of plating. The effectiveness of a TGF-β treatment regimen in enhancing chondrogenesis was correlated with its effectiveness in stimulating condensation formation. Exposures to the factor for 3-6 hr on the day after plating, which most consistently stimulated both condensation formation and chondrogenesis, also corresponded to a peak in the enhancement of the steady-state level of fibronectin mRNA (fourfold to eightfold over control levels) measured at the end of the treatment period. The elevation in fibronectin mRNA levels brought about by this treatment persisted throughout the period of condensation. Endogenous TGF-β-like activity was detected in limb mesenchyme: extracts of freshly isolated and cultured limb tissues contained 6-25 pg TGF-β-like activity per 1 × 106 cells by the Mv1Lu cell proliferation inhibition assay, and indirect immunofluorescence using a polyclonal antibody directed against a TGF-β-related peptide indicated a patchy distribution of endogenous TGF-β-like reactivity within a day after culture. These findings are discussed in relation to the {"}fibronectin prepattern{"} hypothesis for limb pattern formation.",
author = "Leonard, {Claire M.} and Fuld, {Howard M.} and Frenz, {Dorothy A.} and Downie, {Sherry A.} and Joan Massague and Newman, {Stuart A.}",
year = "1991",
doi = "10.1016/0012-1606(91)90216-P",
language = "English (US)",
volume = "145",
pages = "99--109",
journal = "Developmental Biology",
issn = "0012-1606",
publisher = "Academic Press Inc.",
number = "1",

}

TY - JOUR

T1 - Role of transforming growth factor-β in chondrogenic pattern formation in the embryonic limb

T2 - Stimulation of mesenchymal condensation and fibronectin gene expression by exogenenous TGF-β and evidence for endogenous TGF-β-like activity

AU - Leonard, Claire M.

AU - Fuld, Howard M.

AU - Frenz, Dorothy A.

AU - Downie, Sherry A.

AU - Massague, Joan

AU - Newman, Stuart A.

PY - 1991

Y1 - 1991

N2 - The possible role of TGF-β-like molecules in skeletal pattern formation in the embryonic vertebrate limb was studied by analyzing the mechanism of enhancement of chondrogenesis in chick wing bud mesenchyme in vitro and testing for the presence and distribution of endogenous TGF-β-like activity in this tissue. Transient exposure (3-6 hr) to TGF-β1 (1-2 ng/ml) on the day after plating resulted in a 1.5- to 2-fold enhancement of accumulation of Alcian blue (pH 1.0)-stainable extracellular matrix 5 days later. The enhancement of differentiation was preceded by an acceleration and an increase in the extent of precartilage condensation formation, visualized by Hoffman Modulation Contrast microscopy a day after TGF-β treatment. In contrast, neither condensation nor subsequent chondrogenesis was stimulated by transient treatment with TGF-β1 on the day of plating. The effectiveness of a TGF-β treatment regimen in enhancing chondrogenesis was correlated with its effectiveness in stimulating condensation formation. Exposures to the factor for 3-6 hr on the day after plating, which most consistently stimulated both condensation formation and chondrogenesis, also corresponded to a peak in the enhancement of the steady-state level of fibronectin mRNA (fourfold to eightfold over control levels) measured at the end of the treatment period. The elevation in fibronectin mRNA levels brought about by this treatment persisted throughout the period of condensation. Endogenous TGF-β-like activity was detected in limb mesenchyme: extracts of freshly isolated and cultured limb tissues contained 6-25 pg TGF-β-like activity per 1 × 106 cells by the Mv1Lu cell proliferation inhibition assay, and indirect immunofluorescence using a polyclonal antibody directed against a TGF-β-related peptide indicated a patchy distribution of endogenous TGF-β-like reactivity within a day after culture. These findings are discussed in relation to the "fibronectin prepattern" hypothesis for limb pattern formation.

AB - The possible role of TGF-β-like molecules in skeletal pattern formation in the embryonic vertebrate limb was studied by analyzing the mechanism of enhancement of chondrogenesis in chick wing bud mesenchyme in vitro and testing for the presence and distribution of endogenous TGF-β-like activity in this tissue. Transient exposure (3-6 hr) to TGF-β1 (1-2 ng/ml) on the day after plating resulted in a 1.5- to 2-fold enhancement of accumulation of Alcian blue (pH 1.0)-stainable extracellular matrix 5 days later. The enhancement of differentiation was preceded by an acceleration and an increase in the extent of precartilage condensation formation, visualized by Hoffman Modulation Contrast microscopy a day after TGF-β treatment. In contrast, neither condensation nor subsequent chondrogenesis was stimulated by transient treatment with TGF-β1 on the day of plating. The effectiveness of a TGF-β treatment regimen in enhancing chondrogenesis was correlated with its effectiveness in stimulating condensation formation. Exposures to the factor for 3-6 hr on the day after plating, which most consistently stimulated both condensation formation and chondrogenesis, also corresponded to a peak in the enhancement of the steady-state level of fibronectin mRNA (fourfold to eightfold over control levels) measured at the end of the treatment period. The elevation in fibronectin mRNA levels brought about by this treatment persisted throughout the period of condensation. Endogenous TGF-β-like activity was detected in limb mesenchyme: extracts of freshly isolated and cultured limb tissues contained 6-25 pg TGF-β-like activity per 1 × 106 cells by the Mv1Lu cell proliferation inhibition assay, and indirect immunofluorescence using a polyclonal antibody directed against a TGF-β-related peptide indicated a patchy distribution of endogenous TGF-β-like reactivity within a day after culture. These findings are discussed in relation to the "fibronectin prepattern" hypothesis for limb pattern formation.

UR - http://www.scopus.com/inward/record.url?scp=0025732395&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025732395&partnerID=8YFLogxK

U2 - 10.1016/0012-1606(91)90216-P

DO - 10.1016/0012-1606(91)90216-P

M3 - Article

C2 - 2019328

AN - SCOPUS:0025732395

VL - 145

SP - 99

EP - 109

JO - Developmental Biology

JF - Developmental Biology

SN - 0012-1606

IS - 1

ER -