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Transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma

PURPOSE: To clarify the mechanisms of intrauterine platelet‐rich plasma (PRP) infusion that support embryo implantation in in vitro fertilization treatment. METHODS: Blood and endometrial samples were collected from four infertile women. Human endometrial stromal cells (HESCs) were cultured and pass...

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Autores principales: Kuroda, Keiji, Matsumoto, Akemi, Horikawa, Takashi, Takamizawa, Satoru, Ochiai, Asako, Kawamura, Kazuhiro, Nakagawa, Koji, Sugiyama, Rikikazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868347/
https://www.ncbi.nlm.nih.gov/pubmed/36704119
http://dx.doi.org/10.1002/rmb2.12498
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author Kuroda, Keiji
Matsumoto, Akemi
Horikawa, Takashi
Takamizawa, Satoru
Ochiai, Asako
Kawamura, Kazuhiro
Nakagawa, Koji
Sugiyama, Rikikazu
author_facet Kuroda, Keiji
Matsumoto, Akemi
Horikawa, Takashi
Takamizawa, Satoru
Ochiai, Asako
Kawamura, Kazuhiro
Nakagawa, Koji
Sugiyama, Rikikazu
author_sort Kuroda, Keiji
collection PubMed
description PURPOSE: To clarify the mechanisms of intrauterine platelet‐rich plasma (PRP) infusion that support embryo implantation in in vitro fertilization treatment. METHODS: Blood and endometrial samples were collected from four infertile women. Human endometrial stromal cells (HESCs) were cultured and passaged equally into four cell culture dishes in each patient. Two were treated with PRP twice, and the other two were treated with vehicle. Subsequently, two cultures with and without PRP were decidualized with 8‐bromoadenosine 3′,5′‐cyclic AMP and progesterone for 5 days. RESULTS: The gene expression in undifferentiated or decidualized HESCs with and without PRP was compared. In the microarray analysis, 381 and 63 differentially expressed genes were detected in undifferentiated and decidualized HESCs, respectively. In the undifferentiated HESCs, PRP was found to promote the gene expression associated with cell growth, tissue regeneration, proinflammatory response, and antibiotic effects. In decidualized HESCs, PRP was found to attenuate the gene expression involved in cell proliferation and inflammation by inhibiting the expression of phosphoinositide 3‐kinase signaling. CONCLUSIONS: Platelet‐rich plasma regulates the reprogramming of cell proliferation and inflammation depending on menstrual cycle phases in an appropriate manner, suggesting that PRP has the potential to increase endometrial thickness in the proliferative phase and improve immune tolerance in the secretory phase.
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spelling pubmed-98683472023-01-25 Transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma Kuroda, Keiji Matsumoto, Akemi Horikawa, Takashi Takamizawa, Satoru Ochiai, Asako Kawamura, Kazuhiro Nakagawa, Koji Sugiyama, Rikikazu Reprod Med Biol Original Articles PURPOSE: To clarify the mechanisms of intrauterine platelet‐rich plasma (PRP) infusion that support embryo implantation in in vitro fertilization treatment. METHODS: Blood and endometrial samples were collected from four infertile women. Human endometrial stromal cells (HESCs) were cultured and passaged equally into four cell culture dishes in each patient. Two were treated with PRP twice, and the other two were treated with vehicle. Subsequently, two cultures with and without PRP were decidualized with 8‐bromoadenosine 3′,5′‐cyclic AMP and progesterone for 5 days. RESULTS: The gene expression in undifferentiated or decidualized HESCs with and without PRP was compared. In the microarray analysis, 381 and 63 differentially expressed genes were detected in undifferentiated and decidualized HESCs, respectively. In the undifferentiated HESCs, PRP was found to promote the gene expression associated with cell growth, tissue regeneration, proinflammatory response, and antibiotic effects. In decidualized HESCs, PRP was found to attenuate the gene expression involved in cell proliferation and inflammation by inhibiting the expression of phosphoinositide 3‐kinase signaling. CONCLUSIONS: Platelet‐rich plasma regulates the reprogramming of cell proliferation and inflammation depending on menstrual cycle phases in an appropriate manner, suggesting that PRP has the potential to increase endometrial thickness in the proliferative phase and improve immune tolerance in the secretory phase. John Wiley and Sons Inc. 2023-01-22 /pmc/articles/PMC9868347/ /pubmed/36704119 http://dx.doi.org/10.1002/rmb2.12498 Text en © 2023 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Kuroda, Keiji
Matsumoto, Akemi
Horikawa, Takashi
Takamizawa, Satoru
Ochiai, Asako
Kawamura, Kazuhiro
Nakagawa, Koji
Sugiyama, Rikikazu
Transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma
title Transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma
title_full Transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma
title_fullStr Transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma
title_full_unstemmed Transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma
title_short Transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma
title_sort transcriptomic profiling analysis of human endometrial stromal cells treated with autologous platelet‐rich plasma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868347/
https://www.ncbi.nlm.nih.gov/pubmed/36704119
http://dx.doi.org/10.1002/rmb2.12498
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