Comparative study of human eutopic and ectopic endometrial mesenchymal stem cells and the development of an in vivo endometriotic invasion model

Kao AP, An‐Pei Kao, An-Pei Kao, Wang KH, Kai-Hung Wang, Kai‐Hung Wang, Chia-Cheng Chang, Chia‐Cheng Chang, Chang CC, Jau-Nan Lee, Lee JN, Cheng‐Yu Long, Long CY, Cheng-Yu Long, Hung‐Sheng Chen, Chen HS, Hung-Sheng Chen, Cheng‐Fang Tsai, Tsai CF, Cheng-Fang Tsai, Tsung‐Hua Hsieh, Hsieh TH, Tsung-Hua Hsieh, Eing-Mei Tsai, Eing‐Mei Tsai, Tsai EM
Fertility and sterility · 2010 · vol. 95(4) , pp. 1308–1315.e1 · doi:10.1016/j.fertnstert.2010.09.064 · PMID:21047634 · W1974272339
Lab / animal OA: bronze CC0 ⤵ 113 in-corpus citations
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This study compared human eutopic and ectopic endometrial mesenchymal stem cells and developed an in vivo model for endometriotic invasion.

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Abstract

OBJECTIVE: To elucidate the role of endometrial stem-progenitor cells in the etiology of endometriosis and to develop an animal model to study the invasion ability of endometrial cells. DESIGN: Gene expression and cell function studies were designed. SETTING: Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan. PATIENT(S): Human endometrial mesenchymal stem cells (MSCs) were isolated from 22 different endometrium biopsies after surgery for treatment of endometriosis. INTERVENTION(S): Endometrial MSCs developed from eutopic and ectopic endometrial tissues. MAIN OUTCOME MEASURE(S): Characterization of MSC phenotypes (i.e., differentiation induction and gene expression by flow cytometric analysis); comparative study of cell functions (i.e., cell growth, migration, and invasion assays). The invasion of implants in an animal model was examined by histologic staining. RESULT(S): We compared the characteristics of eutopic and ectopic endometrial MSCs from the same endometrial donor. Although both showed similar mesenchymal cell phenotypes, ectopic endometrial MSCs showed distinctly greater ability of cell migration and invasion. Furthermore, in an in vivo cell invasion model using cells grown in scaffold and transplantation in immune-deficient mice, the ectopic endometrial MSCs were found to form many new blood vessels and to invade surrounding tissue. CONCLUSION(S): These results indicate unique invasion and angiogenesis characteristics of ectopic endometrial MSCs that may underlie the pathogenesis of ectopic endometriosis. The animal invasion model will be useful for future characterization of endometrial MSCs.

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Condition tags

endometriosis

MeSH descriptors

Choristoma Choristoma Disease Models, Animal Disease Models, Animal Endometriosis Endometrium Endometrium Mesenchymal Stem Cells Mesenchymal Stem Cell Transplantation Mesenchymal Stem Cell Transplantation Mesenchymal Stem Cell Transplantation Animals Animals Cell Movement Cell Movement Cell Movement Cell Proliferation Cell Proliferation Cells, Cultured Cells, Cultured

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