Luminescence as a Tool to Assess Pelvic Endometriosis Development in Murine Models

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Luminescence techniques, using genetically modified tissue or fluorescent dyes, aid in identifying, visualizing, and quantifying endometriotic transplants in murine models.

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The paper reviews and conceptualizes luminescence-based approaches to measure endometriotic lesion development in murine models, focusing on the challenge that small, tissue-embedded implants can make lesion identification and quantification difficult when assessing therapeutic effects. It describes transplanting luminescently labeled murine or human endometrium into animals, using either genetically modified endometrial tissue or fluorescent dye labeling, and highlights how luminescence enables visualization/quantification as well as endometrial cell tracking with spatial and temporal information in vivo. A key caveat is that the choice between labeling strategies depends on study goals and design, including whether experiments are short- or long-term and whether models are homologous or heterologous. This paper is centrally about endometriosis — it focuses on luminescence tools to assess pelvic endometriosis development in murine models.

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Abstract

Classic murine endometriosis models may be insufficient to evaluate the effect of therapeutic agents on endometriosis development, because the process of identification and measurement of induced lesions is often impeded, as implants are small and embedded in murine tissue. In this context, as summarized in the current review, luminescence techniques have proved useful for identifying and visualizing or quantifying endometriotic transplants. They are also a valuable tool for endometrial cell tracking in live animals, yielding further information by adding spatial and temporal dimensions to biological processes in vivo. Such approaches involve transplanting luminescently labeled murine or human endometrium into animals. Two main strategies are applied to label endometrium before injection: use of genetically modified tissue or tissue labeled with a fluorescent dye. Each model has its advantages and disadvantages, the choice of model depends on the study objectives/design (long- or short-term studies, homologous or heterologous model).
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Abstract

Classic murine endometriosis models may be insufficient to evaluate the effect of therapeutic agents on endometriosis development, because the process of identification and measurement of induced lesions is often impeded, as implants are small and embedded in murine tissue. In this context, as summarized in the current review, luminescence techniques have proved useful for identifying and visualizing or quantifying endometriotic transplants. They are also a valuable tool for endometrial cell tracking in live animals, yielding further information by adding spatial and temporal dimensions to biological processes in vivo. Such approaches involve transplanting luminescently labeled murine or human endometrium into animals. Two main strategies are applied to label endometrium before injection: use of genetically modified tissue or tissue labeled with a fluorescent dye. Each model has its advantages and disadvantages, the choice of model depends on the study objectives/design (long- or short-term studies, homologous or heterologous model). Similar content being viewed by others

References

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Condition tags

endometriosis

MeSH descriptors

Endometriosis Fluorescent Dyes Genes, Reporter Luminescent Measurements Luminescent Proteins Staining and Labeling Animals Disease Models, Animal Endometriosis Endometriosis Endometriosis Endometrium Endometrium Endometrium Female Humans Luminescent Proteins Luminescent Proteins Mice Mice, Transgenic

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