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Endometriosis in the Mouse: Challenges and Progress Toward a ‘Best Fit’ Murine Model

Endometriosis is a prevalent gynecologic condition associated with pelvic pain and infertility characterized by the implantation and growth of endometrial tissue displaced into the pelvis via retrograde menstruation. The mouse is a molecularly well-annotated and cost-efficient species for modeling h...

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Autores principales: Burns, Katherine A., Pearson, Amelia M., Slack, Jessica L., Por, Elaine D., Scribner, Alicia N., Eti, Nazmin A., Burney, Richard O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8794744/
https://www.ncbi.nlm.nih.gov/pubmed/35095566
http://dx.doi.org/10.3389/fphys.2021.806574
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author Burns, Katherine A.
Pearson, Amelia M.
Slack, Jessica L.
Por, Elaine D.
Scribner, Alicia N.
Eti, Nazmin A.
Burney, Richard O.
author_facet Burns, Katherine A.
Pearson, Amelia M.
Slack, Jessica L.
Por, Elaine D.
Scribner, Alicia N.
Eti, Nazmin A.
Burney, Richard O.
author_sort Burns, Katherine A.
collection PubMed
description Endometriosis is a prevalent gynecologic condition associated with pelvic pain and infertility characterized by the implantation and growth of endometrial tissue displaced into the pelvis via retrograde menstruation. The mouse is a molecularly well-annotated and cost-efficient species for modeling human disease in the therapeutic discovery pipeline. However, as a non-menstrual species with a closed tubo-ovarian junction, the mouse poses inherent challenges as a preclinical model for endometriosis research. Over the past three decades, numerous murine models of endometriosis have been described with varying degrees of fidelity in recapitulating the essential pathophysiologic features of the human disease. We conducted a search of the peer-reviewed literature to identify publications describing preclinical research using a murine model of endometriosis. Each model was reviewed according to a panel of ideal model parameters founded on the current understanding of endometriosis pathophysiology. Evaluated parameters included method of transplantation, cycle phase and type of tissue transplanted, recipient immune/ovarian status, iterative schedule of transplantation, and option for longitudinal lesion assessment. Though challenges remain, more recent models have incorporated innovative technical approaches such as in vivo fluorescence imaging and novel hormonal preparations to overcome the unique challenges posed by murine anatomy and physiology. These models offer significant advantages in lesion development and readout toward a high-fidelity mouse model for translational research in endometriosis.
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spelling pubmed-87947442022-01-29 Endometriosis in the Mouse: Challenges and Progress Toward a ‘Best Fit’ Murine Model Burns, Katherine A. Pearson, Amelia M. Slack, Jessica L. Por, Elaine D. Scribner, Alicia N. Eti, Nazmin A. Burney, Richard O. Front Physiol Physiology Endometriosis is a prevalent gynecologic condition associated with pelvic pain and infertility characterized by the implantation and growth of endometrial tissue displaced into the pelvis via retrograde menstruation. The mouse is a molecularly well-annotated and cost-efficient species for modeling human disease in the therapeutic discovery pipeline. However, as a non-menstrual species with a closed tubo-ovarian junction, the mouse poses inherent challenges as a preclinical model for endometriosis research. Over the past three decades, numerous murine models of endometriosis have been described with varying degrees of fidelity in recapitulating the essential pathophysiologic features of the human disease. We conducted a search of the peer-reviewed literature to identify publications describing preclinical research using a murine model of endometriosis. Each model was reviewed according to a panel of ideal model parameters founded on the current understanding of endometriosis pathophysiology. Evaluated parameters included method of transplantation, cycle phase and type of tissue transplanted, recipient immune/ovarian status, iterative schedule of transplantation, and option for longitudinal lesion assessment. Though challenges remain, more recent models have incorporated innovative technical approaches such as in vivo fluorescence imaging and novel hormonal preparations to overcome the unique challenges posed by murine anatomy and physiology. These models offer significant advantages in lesion development and readout toward a high-fidelity mouse model for translational research in endometriosis. Frontiers Media S.A. 2022-01-13 /pmc/articles/PMC8794744/ /pubmed/35095566 http://dx.doi.org/10.3389/fphys.2021.806574 Text en Copyright © 2022 Burns, Pearson, Slack, Por, Scribner, Eti and Burney. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Burns, Katherine A.
Pearson, Amelia M.
Slack, Jessica L.
Por, Elaine D.
Scribner, Alicia N.
Eti, Nazmin A.
Burney, Richard O.
Endometriosis in the Mouse: Challenges and Progress Toward a ‘Best Fit’ Murine Model
title Endometriosis in the Mouse: Challenges and Progress Toward a ‘Best Fit’ Murine Model
title_full Endometriosis in the Mouse: Challenges and Progress Toward a ‘Best Fit’ Murine Model
title_fullStr Endometriosis in the Mouse: Challenges and Progress Toward a ‘Best Fit’ Murine Model
title_full_unstemmed Endometriosis in the Mouse: Challenges and Progress Toward a ‘Best Fit’ Murine Model
title_short Endometriosis in the Mouse: Challenges and Progress Toward a ‘Best Fit’ Murine Model
title_sort endometriosis in the mouse: challenges and progress toward a ‘best fit’ murine model
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8794744/
https://www.ncbi.nlm.nih.gov/pubmed/35095566
http://dx.doi.org/10.3389/fphys.2021.806574
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