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Closer to the Reality—Proteome Changes Evoked by Endometrial Scratching in Fertile Females

Endometrial scratching (ES) has been widely used in assisted reproductive technology to possibly improve pregnancy rates, but its exact mechanism is still not understood or investigated, and its benefits are controversially discussed. Hypothetically, ES may trigger a local immune response, leading t...

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Autores principales: Scheliga, Iwona, Baston-Buest, Dunja M., Poschmann, Gereon, Stuehler, Kai, Kruessel, Jan-Steffen, Bielfeld, Alexandra P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488085/
https://www.ncbi.nlm.nih.gov/pubmed/37686380
http://dx.doi.org/10.3390/ijms241713577
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author Scheliga, Iwona
Baston-Buest, Dunja M.
Poschmann, Gereon
Stuehler, Kai
Kruessel, Jan-Steffen
Bielfeld, Alexandra P.
author_facet Scheliga, Iwona
Baston-Buest, Dunja M.
Poschmann, Gereon
Stuehler, Kai
Kruessel, Jan-Steffen
Bielfeld, Alexandra P.
author_sort Scheliga, Iwona
collection PubMed
description Endometrial scratching (ES) has been widely used in assisted reproductive technology to possibly improve pregnancy rates, but its exact mechanism is still not understood or investigated, and its benefits are controversially discussed. Hypothetically, ES may trigger a local immune response, leading to an improved endometrial receptivity. So far, it has been shown that ES affects the gene expression of cytokines, growth factors, and adhesive proteins, potentially modulating inflammatory pathways and adhesion molecule expression. Our pilot study applying proteomic analysis reveals that ES probably has an impact on the proteins involved in immune response pathways and cytoskeleton formation, which could potentially increase endometrial receptivity. Specifically, proteins that are involved in the immune response and cytoskeleton regulation showed a trend toward higher abundance after the first ES. On the other hand, proteins with a decreasing abundance after the first ES play roles in the regulation of the actin cytoskeleton and cellular processes such as intracellular transport, apoptosis, and autophagy. These trends in protein changes suggest that ES may affect endometrial tissue stiffness and extracellular matrix remodeling, potentially enhancing the embryos’ implantation. To our knowledge, this pilot study provides, for the first time, data investigating potential changes in the endometrium due to the scratching procedure that might explain its possible benefit for patients in infertility treatment. Furthermore, the proteome of a group of patients suffering from repeated implantation failure was compared to that of the fertile group in order to transfer the basic science to clinical routine and application.
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spelling pubmed-104880852023-09-09 Closer to the Reality—Proteome Changes Evoked by Endometrial Scratching in Fertile Females Scheliga, Iwona Baston-Buest, Dunja M. Poschmann, Gereon Stuehler, Kai Kruessel, Jan-Steffen Bielfeld, Alexandra P. Int J Mol Sci Article Endometrial scratching (ES) has been widely used in assisted reproductive technology to possibly improve pregnancy rates, but its exact mechanism is still not understood or investigated, and its benefits are controversially discussed. Hypothetically, ES may trigger a local immune response, leading to an improved endometrial receptivity. So far, it has been shown that ES affects the gene expression of cytokines, growth factors, and adhesive proteins, potentially modulating inflammatory pathways and adhesion molecule expression. Our pilot study applying proteomic analysis reveals that ES probably has an impact on the proteins involved in immune response pathways and cytoskeleton formation, which could potentially increase endometrial receptivity. Specifically, proteins that are involved in the immune response and cytoskeleton regulation showed a trend toward higher abundance after the first ES. On the other hand, proteins with a decreasing abundance after the first ES play roles in the regulation of the actin cytoskeleton and cellular processes such as intracellular transport, apoptosis, and autophagy. These trends in protein changes suggest that ES may affect endometrial tissue stiffness and extracellular matrix remodeling, potentially enhancing the embryos’ implantation. To our knowledge, this pilot study provides, for the first time, data investigating potential changes in the endometrium due to the scratching procedure that might explain its possible benefit for patients in infertility treatment. Furthermore, the proteome of a group of patients suffering from repeated implantation failure was compared to that of the fertile group in order to transfer the basic science to clinical routine and application. MDPI 2023-09-01 /pmc/articles/PMC10488085/ /pubmed/37686380 http://dx.doi.org/10.3390/ijms241713577 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Scheliga, Iwona
Baston-Buest, Dunja M.
Poschmann, Gereon
Stuehler, Kai
Kruessel, Jan-Steffen
Bielfeld, Alexandra P.
Closer to the Reality—Proteome Changes Evoked by Endometrial Scratching in Fertile Females
title Closer to the Reality—Proteome Changes Evoked by Endometrial Scratching in Fertile Females
title_full Closer to the Reality—Proteome Changes Evoked by Endometrial Scratching in Fertile Females
title_fullStr Closer to the Reality—Proteome Changes Evoked by Endometrial Scratching in Fertile Females
title_full_unstemmed Closer to the Reality—Proteome Changes Evoked by Endometrial Scratching in Fertile Females
title_short Closer to the Reality—Proteome Changes Evoked by Endometrial Scratching in Fertile Females
title_sort closer to the reality—proteome changes evoked by endometrial scratching in fertile females
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488085/
https://www.ncbi.nlm.nih.gov/pubmed/37686380
http://dx.doi.org/10.3390/ijms241713577
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