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Novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients

BACKGROUND: Menstrual blood-derived cells show regenerative potential as a mesenchymal stem cell and may therefore be a novel stem cell source of treatment for refractory infertility with injured endometrium. However, there have been few pre-clinical studies using cells from infertile patients, whic...

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Autores principales: Hosoya, Satoshi, Yokomizo, Ryo, Kishigami, Harue, Fujiki, Yukiko, Kaneko, Erika, Amita, Mitsuyoshi, Saito, Takakazu, Kishi, Hiroshi, Sago, Haruhiko, Okamoto, Aikou, Umezawa, Akihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577920/
https://www.ncbi.nlm.nih.gov/pubmed/37840125
http://dx.doi.org/10.1186/s13287-023-03524-z
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author Hosoya, Satoshi
Yokomizo, Ryo
Kishigami, Harue
Fujiki, Yukiko
Kaneko, Erika
Amita, Mitsuyoshi
Saito, Takakazu
Kishi, Hiroshi
Sago, Haruhiko
Okamoto, Aikou
Umezawa, Akihiro
author_facet Hosoya, Satoshi
Yokomizo, Ryo
Kishigami, Harue
Fujiki, Yukiko
Kaneko, Erika
Amita, Mitsuyoshi
Saito, Takakazu
Kishi, Hiroshi
Sago, Haruhiko
Okamoto, Aikou
Umezawa, Akihiro
author_sort Hosoya, Satoshi
collection PubMed
description BACKGROUND: Menstrual blood-derived cells show regenerative potential as a mesenchymal stem cell and may therefore be a novel stem cell source of treatment for refractory infertility with injured endometrium. However, there have been few pre-clinical studies using cells from infertile patients, which need to be addressed before establishing an autologous transplantation. Herein, we aimed to investigate the therapeutic capacity of menstrual blood-derived cells from infertile patients on endometrial infertility. METHODS: We collected menstrual blood-derived cells from volunteers and infertile patients and confirmed their mesenchymal stem cell phenotype by flow cytometry and induction of tri-lineage differentiation. We compared the proliferative and paracrine capacities of these cells. Furthermore, we also investigated the regenerative potential and safety concerns of the intrauterine transplantation of infertile patient-derived cells using a mouse model with mechanically injured endometrium. RESULTS: Menstrual blood-derived cells from both infertile patients and volunteers showed phenotypic characteristics of mesenchymal stem cells. In vitro proliferative and paracrine capacities for wound healing and angiogenesis were equal for both samples. Furthermore, the transplantation of infertile patient-derived cells into uterine horns of the mouse model ameliorated endometrial thickness, prevented fibrosis, and improved fertility outcomes without any apparent complications. CONCLUSIONS: In our pre-clinical study, intrauterine transplantation of menstrual blood-derived cells may be a novel and attractive stem cell source for the curative and prophylactic therapy for injured endometrium. Further studies will be warranted for future clinical application. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03524-z.
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spelling pubmed-105779202023-10-17 Novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients Hosoya, Satoshi Yokomizo, Ryo Kishigami, Harue Fujiki, Yukiko Kaneko, Erika Amita, Mitsuyoshi Saito, Takakazu Kishi, Hiroshi Sago, Haruhiko Okamoto, Aikou Umezawa, Akihiro Stem Cell Res Ther Research BACKGROUND: Menstrual blood-derived cells show regenerative potential as a mesenchymal stem cell and may therefore be a novel stem cell source of treatment for refractory infertility with injured endometrium. However, there have been few pre-clinical studies using cells from infertile patients, which need to be addressed before establishing an autologous transplantation. Herein, we aimed to investigate the therapeutic capacity of menstrual blood-derived cells from infertile patients on endometrial infertility. METHODS: We collected menstrual blood-derived cells from volunteers and infertile patients and confirmed their mesenchymal stem cell phenotype by flow cytometry and induction of tri-lineage differentiation. We compared the proliferative and paracrine capacities of these cells. Furthermore, we also investigated the regenerative potential and safety concerns of the intrauterine transplantation of infertile patient-derived cells using a mouse model with mechanically injured endometrium. RESULTS: Menstrual blood-derived cells from both infertile patients and volunteers showed phenotypic characteristics of mesenchymal stem cells. In vitro proliferative and paracrine capacities for wound healing and angiogenesis were equal for both samples. Furthermore, the transplantation of infertile patient-derived cells into uterine horns of the mouse model ameliorated endometrial thickness, prevented fibrosis, and improved fertility outcomes without any apparent complications. CONCLUSIONS: In our pre-clinical study, intrauterine transplantation of menstrual blood-derived cells may be a novel and attractive stem cell source for the curative and prophylactic therapy for injured endometrium. Further studies will be warranted for future clinical application. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03524-z. BioMed Central 2023-10-15 /pmc/articles/PMC10577920/ /pubmed/37840125 http://dx.doi.org/10.1186/s13287-023-03524-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hosoya, Satoshi
Yokomizo, Ryo
Kishigami, Harue
Fujiki, Yukiko
Kaneko, Erika
Amita, Mitsuyoshi
Saito, Takakazu
Kishi, Hiroshi
Sago, Haruhiko
Okamoto, Aikou
Umezawa, Akihiro
Novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients
title Novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients
title_full Novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients
title_fullStr Novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients
title_full_unstemmed Novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients
title_short Novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients
title_sort novel therapeutic strategies for injured endometrium: intrauterine transplantation of menstrual blood‑derived cells from infertile patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577920/
https://www.ncbi.nlm.nih.gov/pubmed/37840125
http://dx.doi.org/10.1186/s13287-023-03524-z
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