» Articles » PMID: 19473554

Hypoxia. Hypoxia in the Pathogenesis of Systemic Sclerosis

Overview
Publisher Biomed Central
Specialty Rheumatology
Date 2009 May 29
PMID 19473554
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

Autoimmunity, microangiopathy and tissue fibrosis are hallmarks of systemic sclerosis (SSc). Vascular alterations and reduced capillary density decrease blood flow and impair tissue oxygenation in SSc. Oxygen supply is further reduced by accumulation of extracellular matrix (ECM), which increases diffusion distances from blood vessels to cells. Therefore, severe hypoxia is a characteristic feature of SSc and might contribute directly to the progression of the disease. Hypoxia stimulates the production of ECM proteins by SSc fibroblasts in a transforming growth factor-beta-dependent manner. The induction of ECM proteins by hypoxia is mediated via hypoxia-inducible factor-1alpha-dependent and -independent pathways. Hypoxia may also aggravate vascular disease in SSc by perturbing vascular endothelial growth factor (VEGF) receptor signalling. Hypoxia is a potent inducer of VEGF and may cause chronic VEGF over-expression in SSc. Uncontrolled over-expression of VEGF has been shown to have deleterious effects on angiogenesis because it leads to the formation of chaotic vessels with decreased blood flow. Altogether, hypoxia might play a central role in pathogenesis of SSc by augmenting vascular disease and tissue fibrosis.

Citing Articles

Use of nailfold capillaroscopy for the assessment of patients undergoing digit replantation and revascularization.

Koroglu M, Karakaplan M, Zontul S, Acet O, Ozdes H, Ergen E Jt Dis Relat Surg. 2024; 36(1):65-77.

PMID: 39719903 PMC: 11734863. DOI: 10.52312/jdrs.2025.1900.


Exploring Anti-Fibrotic Effects of Adipose-Derived Stem Cells: Transcriptome Analysis upon Fibrotic, Inflammatory, and Hypoxic Conditioning.

Frommer M, Langridge B, Beedie A, Jasionowska S, Awad L, Denton C Cells. 2024; 13(8.

PMID: 38667308 PMC: 11049044. DOI: 10.3390/cells13080693.


The Role of Small Airway Disease in Pulmonary Fibrotic Diseases.

Barkas G, Daniil Z, Kotsiou O J Pers Med. 2023; 13(11).

PMID: 38003915 PMC: 10672167. DOI: 10.3390/jpm13111600.


Endothelial Dysfunction in Systemic Sclerosis.

Patnaik E, Lyons M, Tran K, Pattanaik D Int J Mol Sci. 2023; 24(18).

PMID: 37762689 PMC: 10531630. DOI: 10.3390/ijms241814385.


Mechanisms and application strategies of miRNA‑146a regulating inflammation and fibrosis at molecular and cellular levels (Review).

Liao Z, Zheng R, Shao G Int J Mol Med. 2022; 51(1).

PMID: 36484394 PMC: 9747201. DOI: 10.3892/ijmm.2022.5210.


References
1.
Maxwell P, Wiesener M, Chang G, Clifford S, Vaux E, Cockman M . The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis. Nature. 1999; 399(6733):271-5. DOI: 10.1038/20459. View

2.
Silverstein J, Steen V, Medsger Jr T, Falanga V . Cutaneous hypoxia in patients with systemic sclerosis (scleroderma). Arch Dermatol. 1988; 124(9):1379-82. View

3.
Ivan M, Kondo K, Yang H, Kim W, Valiando J, Ohh M . HIFalpha targeted for VHL-mediated destruction by proline hydroxylation: implications for O2 sensing. Science. 2001; 292(5516):464-8. DOI: 10.1126/science.1059817. View

4.
Kietzmann T, Cornesse Y, Brechtel K, Modaressi S, Jungermann K . Perivenous expression of the mRNA of the three hypoxia-inducible factor alpha-subunits, HIF1alpha, HIF2alpha and HIF3alpha, in rat liver. Biochem J. 2001; 354(Pt 3):531-7. PMC: 1221684. DOI: 10.1042/0264-6021:3540531. View

5.
Jaakkola P, Mole D, Tian Y, Wilson M, Gielbert J, Gaskell S . Targeting of HIF-alpha to the von Hippel-Lindau ubiquitylation complex by O2-regulated prolyl hydroxylation. Science. 2001; 292(5516):468-72. DOI: 10.1126/science.1059796. View