Fetal cells of mesenchymal origin in cultures derived from synovial tissue and skin of patients with rheumatoid arthritis
Language English Country France Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18538621
DOI
10.1016/j.jbspin.2008.02.004
PII: S1297-319X(08)00103-6
Knihovny.cz E-resources
- MeSH
- Chimerism MeSH
- DNA analysis MeSH
- Adult MeSH
- Fibroblasts chemistry MeSH
- Genetic Markers genetics MeSH
- Cells, Cultured MeSH
- Skin cytology MeSH
- Humans MeSH
- Mesoderm cytology growth & development MeSH
- Young Adult MeSH
- Fetus cytology MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Sex-Determining Region Y Protein genetics MeSH
- Arthritis, Rheumatoid complications MeSH
- Synovectomy MeSH
- Synovial Membrane chemistry cytology MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA MeSH
- Genetic Markers MeSH
- Sex-Determining Region Y Protein MeSH
- SRY protein, human MeSH Browser
The transplacental cell transfer naturally takes place during pregnancy and occurs bi-directionally between the mother and fetus. Using real-time polymerase chain reaction (PCR) assay and sex determining region Y (SRY) gene as a marker, we examined the presence of male fetal cells in cell cultures derived from synovial tissues and skin dermis in women with prior pregnancy history suffering from rheumatoid arthritis (RA) who underwent synovectomy. Male DNA was detected in synovial cell samples derived from carpal, hip, metacarpophalangeal and metatarsophalangeal joints in five out of 13 (38.5%) patients with RA in a frequency range of 0.02-62.55 (mean 12.17) male cells per 10,000,000 total cells. SRY gene positivity was found as well in skin fibroblast cultures in four out of 10 (40.0%) RA patients in a frequency range of 3.26-43.47 (mean 15.42) male cells per 10,000,000 total cells, respectively. The difference in a frequency of fetal-derived male cells between both the cohorts did not achieve the statistical difference (p=0.77). We conclude that persisting male fetal cells are able to grow from non-inflamed tissues as well as from those which have many features characteristic of a stressed tissue. We conclude that persisting male fetal cells are also able to proliferate in cell culture since their presence was detected even in consecutive passages.
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