» Articles » PMID: 15277239

Thy-1 Expression Regulates the Ability of Rat Lung Fibroblasts to Activate Transforming Growth Factor-beta in Response to Fibrogenic Stimuli

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 2004 Jul 28
PMID 15277239
Citations 62
Authors
Affiliations
Soon will be listed here.
Abstract

Distinct subpopulations of fibroblasts contribute to lung fibrosis, although the mechanisms underlying fibrogenesis in these subpopulations are not clear. Differential expression of the glycophosphatidylinositol-linked protein Thy-1 affects proliferation and myofibroblast differentiation. Lung fibroblast populations selected on the basis of Thy-1 expression by cell sorting were examined for responses to fibrogenic stimuli. Thy-1 (-) and Thy-1 (+) fibroblast populations were treated with platelet-derived growth factor-BB, interleukin-1beta, interleukin-4, or bleomycin and assessed for activation of transforming growth factor (TGF)-beta, Smad3 phosphorylation, and alpha-smooth muscle actin and fibronectin expression. Thy-1 (-) fibroblasts responded to these stimuli with increased TGF-beta activity, Smad3 phosphorylation, and expression of alpha-smooth muscle actin and fibronectin, whereas Thy-1 (+) fibroblasts resisted stimulation. The unresponsiveness of Thy-1 (+) cells is not because of defective TGF-beta signaling because both subsets respond to exogenous active TGF-beta. Rather, Thy-1 (-) fibroblasts activate latent TGF-beta in response to fibrogenic stimuli, whereas Thy-1 (+) cells fail to do so. Defective activation is common to multiple mechanisms of TGF-beta activation, including thrombospondin 1, matrix metalloproteinase, or plasmin. Thy-1 (-) lung fibroblasts transfected with Thy-1 also become resistant to fibrogenic stimulation, indicating that Thy-1 is a critical biological response modifier that protects against fibrotic progression by controlling TGF-beta activation. These studies provide a molecular basis for understanding the differential roles of fibroblast subpopulations in fibrotic lung disease through control of latent TGF-beta activation.

Citing Articles

Fibroblast Activation Protein Alpha (FAPα) in Fibrosis: Beyond a Perspective Marker for Activated Stromal Cells?.

Basalova N, Alexandrushkina N, Grigorieva O, Kulebyakina M, Efimenko A Biomolecules. 2023; 13(12).

PMID: 38136590 PMC: 10742035. DOI: 10.3390/biom13121718.


Thy-1 (CD90)-regulated cell adhesion and migration of mesenchymal cells: insights into adhesomes, mechanical forces, and signaling pathways.

Valdivia A, Avalos A, Leyton L Front Cell Dev Biol. 2023; 11:1221306.

PMID: 38099295 PMC: 10720913. DOI: 10.3389/fcell.2023.1221306.


Characterization of Central and Nasal Orbital Adipose Stem Cells and their Neural Differentiation Footprints.

Sanie-Jahromi F, Nowroozzadeh M, Shaabanian M, Khademi B, Owji N, Mehrabani D Curr Stem Cell Res Ther. 2023; 19(8):1111-1119.

PMID: 37670706 DOI: 10.2174/1574888X19666230905114246.


Antifibrotic Soluble Thy-1 Correlates with Renal Dysfunction in Chronic Kidney Disease.

Saalbach A, Anderegg U, Wendt R, Beige J, Bachmann A, Kloting N Int J Mol Sci. 2023; 24(3).

PMID: 36768219 PMC: 9916214. DOI: 10.3390/ijms24031896.


Role and mechanism of CD90 fibroblasts in inflammatory diseases and malignant tumors.

Zeng F, Gao M, Liao S, Zhou Z, Luo G, Zhou Y Mol Med. 2023; 29(1):20.

PMID: 36747131 PMC: 9900913. DOI: 10.1186/s10020-023-00616-7.


References
1.
Phan S . The myofibroblast in pulmonary fibrosis. Chest. 2002; 122(6 Suppl):286S-289S. DOI: 10.1378/chest.122.6_suppl.286s. View

2.
Yehualaeshet T, OConnor R, Green-Johnson J, Mai S, SILVERSTEIN R, Murphy-Ullrich J . Activation of rat alveolar macrophage-derived latent transforming growth factor beta-1 by plasmin requires interaction with thrombospondin-1 and its cell surface receptor, CD36. Am J Pathol. 1999; 155(3):841-51. PMC: 1866879. DOI: 10.1016/s0002-9440(10)65183-8. View

3.
Yehualaeshet T, OConnor R, Begleiter A, Murphy-Ullrich J, SILVERSTEIN R, Khalil N . A CD36 synthetic peptide inhibits bleomycin-induced pulmonary inflammation and connective tissue synthesis in the rat. Am J Respir Cell Mol Biol. 2000; 23(2):204-12. DOI: 10.1165/ajrcmb.23.2.4089. View

4.
Fonseca C, Abraham D, Black C . Lung fibrosis. Springer Semin Immunopathol. 2000; 21(4):453-74. DOI: 10.1007/s002810000036. View

5.
Lasky J, Brody A . Interstitial fibrosis and growth factors. Environ Health Perspect. 2000; 108 Suppl 4:751-62. PMC: 1637668. DOI: 10.1289/ehp.00108s4751. View