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논문 기본 정보

자료유형
학술저널
저자정보
Kim Hee-Yeon (Ewha Womans University College of Medicine) Yoon Hee-Soo (Ewha Womans University College of Medicine) Lee Younghay (Ewha Womans University College of Medicine) Kim Yu-Hee (Ewha Womans University College of Medicine) 조경아 (이화여자대학교) Woo So-Youn (Ewha Womans University College of Medicine) 김한수 (이화여자대학교) 유경하 (이화여자대학교) Park Joo-Won (Ewha Womans University College of Medicine)
저널정보
한국조직공학과 재생의학회 조직공학과 재생의학 조직공학과 재생의학 제20권 제2호
발행연도
2023.4
수록면
271 - 284 (14page)
DOI
10.1007/s13770-022-00501-0

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Background: To achieve optimal bone marrow engraftment during bone marrow transplantation, migration of donor bone marrow cells (BMCs) toward the recipient’s bone marrow is critical. Despite the enhanced engraftment of BMCs by co-administration of mesenchymal stem cells (MSCs), the efficiency can be variable depending on MSC donor. The purpose of this study is to examine the functional heterogeneity of tonsil-derived MSCs (TMSCs) and to identify a marker to evaluate efficacy for the enhancement of BMC migration. Methods: To examine the donor-to-donor variation of TMSCs in potentiating BMC migration, we isolated TMSCs from 25 independent donors. Transcriptome of TMSCs and proteome of conditioned medium derived from TMSC were analyzed. Results: Enhanced BMC migration by conditioned medium derived from TMSCs was variable depending on TMSC donor. The TMSCs derived from 25 donors showed distinct expression profiles compared with other cells, including fibroblasts, adipose-derived MSCs and bone marrow–derived MSCs. TMSCs were distributed in two categories: high- and low-efficacy groups for potentiating BMC migration. Transcriptome analysis of TMSCs and proteome profiles of conditioned medium derived from TMSCs revealed higher expression and secretion of matrix metalloproteinase (MMP) 1 in the high-efficacy group. MMP1 knockdown in TMSCs abrogated the supportive efficacy of conditioned medium derived from TMSC cultures in BMC migration. Conclusion: These data suggest that secreted MMP1 can be used as a marker to evaluate the efficacy of TMSCs in enhancing BMC migration. Furthermore, the strategy of analyzing transcriptomes and proteomes of the MSCs may be useful to set the standard for donor variation.

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