Evaluating the effect of conditioned medium from endometrial stem cells on endometriosis-derived endometrial stem cells.

Conditioned Medium Endometriosis Mesenchymal stem cells

Journal

Anatomy & cell biology
ISSN: 2093-3665
Titre abrégé: Anat Cell Biol
Pays: Korea (South)
ID NLM: 101531987

Informations de publication

Date de publication:
31 Mar 2022
Historique:
received: 23 08 2021
revised: 30 09 2021
accepted: 30 09 2021
pubmed: 28 1 2022
medline: 28 1 2022
entrez: 27 1 2022
Statut: ppublish

Résumé

Endometriosis is a common, benign gynecological disease which is determined as an overspreading of endometrial tissue in exterior region of the uterine cavity. Evidence suggests that retrograde menstrual blood which contains mesenchymal stem cells with differential gene expression compared to healthy women may play a role in endometriosis creation. We aimed to identify whether the conditioned medium (CM) from menstrual blood-derived mesenchymal stem cells (MenSCs) of healthy women can affect the expression level of inflammatory and stemness genes of MenSCs from endometriosis women. Endometriosis-derived MenSCs (E-MenSCs) were treated with CM derived from healthy women's MenSCs (non-endometriosis derived MenSCs [NE-MenSCs]). Some CD markers were analyzed by flow cytometer before and after treatment compared with NE-MenSCs, and the expression level of inflammatory and stemness genes was evaluated by real-time PCR. E-MenSCs show different morphology in vitro culture in comparison with NE-MenSCs, which were changed in the presence of CM, into a morphology more similar to normal cells and showed significant decrease expression of CD10 after CM treatment. In our results, the interleukin-1, cyclooxygenase-2, and hypoxia-inducible factor 1α as inflamaturay genes and octamer-binding transcription factor 4, NANOG, and sex determining region Y-box 2 as stemness genes showed significantly different expression level in E-MenSCs after treating with CM. Our study indicates that the expression level of some inflammatory- and stemness-related genes which have differential expression in E-MenSCs compared with NEMenSCs, could be changed to normal status by using CM derived from NE-MenSCs.

Identifiants

pubmed: 35082175
pii: acb.21.169
doi: 10.5115/acb.21.169
pmc: PMC8968229
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100-108

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Auteurs

Seyedeh Saeideh Sahraei (SS)

Department of Mesenchymal Stem Cells, The Academic Centre for Education, Culture and Research, Qom, Iran.
Department of Reproductive Biology, The Academic Centre for Education, Culture and Research, Qom, Iran.

Ali Kowsari (A)

Department of Mesenchymal Stem Cells, The Academic Centre for Education, Culture and Research, Qom, Iran.

Faezeh Davoodi Asl (FD)

Department of Mesenchymal Stem Cells, The Academic Centre for Education, Culture and Research, Qom, Iran.

Mohsen Sheykhhasan (M)

Department of Mesenchymal Stem Cells, The Academic Centre for Education, Culture and Research, Qom, Iran.

Leila Naserpoor (L)

Department of Reproductive Biology, The Academic Centre for Education, Culture and Research, Qom, Iran.

Azar Sheikholeslami (A)

Department of Mesenchymal Stem Cells, The Academic Centre for Education, Culture and Research, Qom, Iran.

Classifications MeSH