Cited by 119Pregnancy and preeclampsia studiesReproductive System and PregnancyNeonatal and fetal brain pathology

Placental Extracellular Matrix: Gene Expression, Deposition by Placental Fibroblasts and the Effect of Oxygen

Chen, C.P, Aplin, J.D·2003·Placenta

Abstract

Database mining revealed 102 extracellular matrix (ECM) genes amongst about 10000 mRNA species expressed in human placenta, and these were classified into collagens (23), non-collagenous glycoproteins (59) and proteoglycans (23). A panel of antibodies to selected collagens and glycoproteins was used to examine ECM distribution in the placental villous stroma. Collagens I and IV, fibronectin and fibrillin I were abundant in first trimester and term tissue. Some areas lacked collagen I, while collagen IV was clearly evident in interstitial locations. At term, laminin was present in the stroma as well as in trophoblastic and vascular basement membranes. Thrombospondin I, tenascin C and elastin showed more restricted distributions. Fibrosis has been reported in association with ischaemia, so ECM production by cultured term and first trimester placental fibroblasts was evaluated at three different oxygen concentrations. Fibronectin and collagen IV were more strongly expressed than collagen I, fibrillin I or thrombospondin I, while the production of laminin and elastin was very low. Reducing the oxygen tension led to a selective increase in fibronectin and collagen IV production. Thus both quantitative and qualitative alterations in ECM composition may be expected to accompany prolonged hypoxia.

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Crossref · 10.1053/plac.2002.0904

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  • A number of other transcription factors and co-activators respond to changes in the redox potential of a cell rather than to oxygen directly, including AP-1, CREB, Mash2, NFκB, p53, PCC-1α, SP-1 and STAT3.

    “A number of other transcription factors and co-activators have been identified that respond to changes in the redox potential of a cell rather than to oxygen directly.These include AP-1, CREB, Mash2, NFκB, p53, PCC-1α, SP-1 and STAT3 (16, 106, 155, 277).”

    From Placental Origins of Chronic Disease (2016) · cites this paper as [106]

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References 50 · Cited by 119

Authors
Chen, C. P., & Aplin, J. D.
Affiliations
University of Manchester (GB)
Venue
Placenta
Publisher
Elsevier BV
Published
2003-04
Volume
24
Issue
4
Pages
316-325
ISSN
0143-4004 (ISSN-L)
OpenAlex
W2161870241
Cited by
119
References
50
Citations by year
2026: 4 · 2025: 6 · 2024: 9 · 2023: 7 · 2022: 5 · 2021: 9 · 2020: 7 · 2019: 4 · 2018: 3 · 2017: 3 · 2016: 6 · 2015: 4 · 2014: 2 · 2013: 1 · 2012: 4
FWCI
7.66
Type
journal article
Language
en
Open access
closed
Locations
  • Placenta (publishedVersion)
  • PubMed (publishedVersion)
  • Research Explorer (The University of Manchester) (submittedVersion)
Topics
  • Health Sciences › Medicine › Obstetrics and Gynecology › Pregnancy and preeclampsia studies
  • Life Sciences › Immunology and Microbiology › Immunology › Reproductive System and Pregnancy
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Neonatal and fetal brain pathology
Keywords
placental fibroblasts, gene expression, collagen, fibronectin, type IV collagen, laminin, tenascin-C, elastin, hypoxia, oxygen partial pressure, fibrosis, ischemia, first trimester, term placenta
MeSH terms
Adult, Cells, Cultured, Chorionic Villi, Dose-Response Relationship, Drug, Enzyme-Linked Immunosorbent Assay, Extracellular Matrix, Female, Fibroblasts, Humans, Labor, Obstetric, Oxygen, Pregnancy, Pregnancy Trimester, First, RNA, Messenger, Cell Hypoxia, Gene Expression, Extracellular Matrix Proteins, Fluorescent Antibody Technique, Indirect

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