Literature DB >> 18538621

Fetal cells of mesenchymal origin in cultures derived from synovial tissue and skin of patients with rheumatoid arthritis.

Ilona Hromadnikova1, Denisa Zlacka, Thi Thu Hien Nguyen, Lucie Sedlackova, Lenka Zejskova, Antonin Sosna.   

Abstract

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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Year:  2008        PMID: 18538621     DOI: 10.1016/j.jbspin.2008.02.004

Source DB:  PubMed          Journal:  Joint Bone Spine        ISSN: 1297-319X            Impact factor:   4.929


  7 in total

1.  Microchimerism in the rheumatoid nodules of patients with rheumatoid arthritis.

Authors:  William F N Chan; Christopher J Atkins; David Naysmith; Nicholas van der Westhuizen; Janet Woo; J Lee Nelson
Journal:  Arthritis Rheum       Date:  2012-02

2.  Lack of Evidence That Male Fetal Microchimerism is Present in Endometriosis.

Authors:  Amelie Fassbender; Maria Debiec-Rychter; Rieta Van Bree; Joris Robert Vermeesch; Christel Meuleman; Carla Tomassetti; Karen Peeraer; Thomas D'Hooghe; Dan I Lebovic
Journal:  Reprod Sci       Date:  2015-03-05       Impact factor: 3.060

3.  The role of fetal microchimerism in autoimmune disease.

Authors:  Ralph P Miech
Journal:  Int J Clin Exp Med       Date:  2010-06-12

4.  Sarcococca saligna extract attenuates formaldehyde-induced arthritis in Wistar rats via modulation of pro-inflammatory and inflammatory biomarkers.

Authors:  Maryam Farrukh; Uzma Saleem; Muhammad Qasim; Maria Manan; Muhammad Ajmal Shah
Journal:  Inflammopharmacology       Date:  2022-02-26       Impact factor: 4.473

5.  The occurrence of fetal microchimeric cells in endometrial tissues is a very common phenomenon in benign uterine disorders, and the lower prevalence of fetal microchimerism is associated with better uterine cancer prognoses.

Authors:  Ilona Hromadnikova; Katerina Kotlabova; Petra Pirkova; Pavla Libalova; Zdenka Vernerova; Bohuslav Svoboda; Eduard Kucera
Journal:  DNA Cell Biol       Date:  2013-11-27       Impact factor: 3.311

Review 6.  Fetal microchimeric cells in autoimmune thyroid diseases: harmful, beneficial or innocent for the thyroid gland?

Authors:  Trees Lepez; Mado Vandewoestyne; Dieter Deforce
Journal:  Chimerism       Date:  2013-05-20

7.  Long-term persistence and effects of fetal microchimerisms on disease onset and status in a cohort of women with rheumatoid arthritis and systemic lupus erythematosus.

Authors:  Marianne Kekow; Maria Barleben; Susanne Drynda; Sibylle Jakubiczka; Jörn Kekow; Thomas Brune
Journal:  BMC Musculoskelet Disord       Date:  2013-11-18       Impact factor: 2.362

  7 in total

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