The Presence of Pre-Existing Endometriotic Lesions Promotes the Growth of New Lesions in the Peritoneal Cavity
Endometriosis is a common gynecological disease which is characterized by endometriotic lesions outside the uterine cavity. In this study, we investigated whether the presence of pre-existing endometriotic lesions promotes the development of new lesions due to the exchange of cells and an altered pe...
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Veröffentlicht in: | International journal of molecular sciences 2023-09, Vol.24 (18), p.13858 |
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description | Endometriosis is a common gynecological disease which is characterized by endometriotic lesions outside the uterine cavity. In this study, we investigated whether the presence of pre-existing endometriotic lesions promotes the development of new lesions due to the exchange of cells and an altered peritoneal environment. For this purpose, uterine tissue samples from FVB/N wild-type donor mice were transplanted simultaneously or time-delayed with samples from transgenic FVB-Tg(CAG-luc-GFP)L2G85Chco/J donor mice into the abdominal cavity of FVB/N wild-type recipient mice. The formation of endometriotic lesions was analyzed by means of high-resolution ultrasound, bioluminescence imaging, histology and immunohistochemistry. Moreover, immune cells and inflammatory factors in the peritoneal fluid were assessed by flow cytometry and a cytokine array. These analyses revealed that the growth of newly developing endometriotic lesions is promoted by the presence of pre-existing ones. This is not due to an exchange of cells between both lesion types but rather caused by peritoneal inflammation induced by already established lesions. These findings indicate that, among other pathogenic mechanisms, the chronic nature of endometriosis may be driven by a lesion-induced inflammatory milieu in the peritoneal cavity, which creates favorable conditions for the development of new lesions. |
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In this study, we investigated whether the presence of pre-existing endometriotic lesions promotes the development of new lesions due to the exchange of cells and an altered peritoneal environment. For this purpose, uterine tissue samples from FVB/N wild-type donor mice were transplanted simultaneously or time-delayed with samples from transgenic FVB-Tg(CAG-luc-GFP)L2G85Chco/J donor mice into the abdominal cavity of FVB/N wild-type recipient mice. The formation of endometriotic lesions was analyzed by means of high-resolution ultrasound, bioluminescence imaging, histology and immunohistochemistry. Moreover, immune cells and inflammatory factors in the peritoneal fluid were assessed by flow cytometry and a cytokine array. These analyses revealed that the growth of newly developing endometriotic lesions is promoted by the presence of pre-existing ones. This is not due to an exchange of cells between both lesion types but rather caused by peritoneal inflammation induced by already established lesions. These findings indicate that, among other pathogenic mechanisms, the chronic nature of endometriosis may be driven by a lesion-induced inflammatory milieu in the peritoneal cavity, which creates favorable conditions for the development of new lesions.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms241813858</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Abdomen ; Bioluminescence ; Cysts ; Cytokines ; Endometriosis ; Experiments ; Flow cytometry ; Genetic engineering ; Granulocytes ; Growth ; Gynecological diseases ; Immunohistochemistry ; Lymphocytes ; Menstruation ; Physiology ; Transgenic animals ; Ultrasonic imaging ; Uterus</subject><ispartof>International journal of molecular sciences, 2023-09, Vol.24 (18), p.13858</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. 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/). 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In this study, we investigated whether the presence of pre-existing endometriotic lesions promotes the development of new lesions due to the exchange of cells and an altered peritoneal environment. For this purpose, uterine tissue samples from FVB/N wild-type donor mice were transplanted simultaneously or time-delayed with samples from transgenic FVB-Tg(CAG-luc-GFP)L2G85Chco/J donor mice into the abdominal cavity of FVB/N wild-type recipient mice. The formation of endometriotic lesions was analyzed by means of high-resolution ultrasound, bioluminescence imaging, histology and immunohistochemistry. Moreover, immune cells and inflammatory factors in the peritoneal fluid were assessed by flow cytometry and a cytokine array. These analyses revealed that the growth of newly developing endometriotic lesions is promoted by the presence of pre-existing ones. This is not due to an exchange of cells between both lesion types but rather caused by peritoneal inflammation induced by already established lesions. These findings indicate that, among other pathogenic mechanisms, the chronic nature of endometriosis may be driven by a lesion-induced inflammatory milieu in the peritoneal cavity, which creates favorable conditions for the development of new lesions.</description><subject>Abdomen</subject><subject>Bioluminescence</subject><subject>Cysts</subject><subject>Cytokines</subject><subject>Endometriosis</subject><subject>Experiments</subject><subject>Flow cytometry</subject><subject>Genetic engineering</subject><subject>Granulocytes</subject><subject>Growth</subject><subject>Gynecological diseases</subject><subject>Immunohistochemistry</subject><subject>Lymphocytes</subject><subject>Menstruation</subject><subject>Physiology</subject><subject>Transgenic animals</subject><subject>Ultrasonic imaging</subject><subject>Uterus</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkk1PGzEQhldVK5ECR-4r9dLLUn_t2j6hKEpppQg40LPldcaJo1072E4o_75OQdBU2AePPM_7jmY0VXWB0SWlEn1zmzERhgWmohUfqglmhDQIdfzjP_FJ9TmlDUKEklZOKn-_hvouQgJvoA72EDfz3y5l51f13C_DCDm6kJ2pF5Bc8KkgYQwZUp2L9jqGx7w-KG_g8RVx_m_yDqLLwYMe6pneu_x0Vn2yekhw_vKeVr--z-9nP5rF7fXP2XTRGNah3OAOCck0kcT0fc-ACWxxK6AnjBjKxVJqzThmgKRAxHBKCTDbctr2FriV9LS6evbd7voRlgZ8jnpQ2-hGHZ9U0E4dZ7xbq1XYK4xaionsisPXF4cYHnaQshpdMjAM2kPYJUUER2XQ5RT0y3_oJuyiL_0VqpOUEyrQG7XSAyjnbSiFzcFUTTnHheAtLtTlO1S5SxidKaO0rvwfCZpngYkhpQj2tUmM1GEt1NFa0D-UK6p1</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Mihai, Ilinca T</creator><creator>Rudzitis-Auth, Jeannette</creator><creator>Menger, Michael D</creator><creator>Laschke, Matthias W</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2047-2297</orcidid><orcidid>https://orcid.org/0000-0002-7847-8456</orcidid><orcidid>https://orcid.org/0000-0002-9670-7961</orcidid></search><sort><creationdate>20230901</creationdate><title>The Presence of Pre-Existing Endometriotic Lesions Promotes the Growth of New Lesions in the Peritoneal Cavity</title><author>Mihai, Ilinca T ; 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In this study, we investigated whether the presence of pre-existing endometriotic lesions promotes the development of new lesions due to the exchange of cells and an altered peritoneal environment. For this purpose, uterine tissue samples from FVB/N wild-type donor mice were transplanted simultaneously or time-delayed with samples from transgenic FVB-Tg(CAG-luc-GFP)L2G85Chco/J donor mice into the abdominal cavity of FVB/N wild-type recipient mice. The formation of endometriotic lesions was analyzed by means of high-resolution ultrasound, bioluminescence imaging, histology and immunohistochemistry. Moreover, immune cells and inflammatory factors in the peritoneal fluid were assessed by flow cytometry and a cytokine array. These analyses revealed that the growth of newly developing endometriotic lesions is promoted by the presence of pre-existing ones. This is not due to an exchange of cells between both lesion types but rather caused by peritoneal inflammation induced by already established lesions. These findings indicate that, among other pathogenic mechanisms, the chronic nature of endometriosis may be driven by a lesion-induced inflammatory milieu in the peritoneal cavity, which creates favorable conditions for the development of new lesions.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/ijms241813858</doi><orcidid>https://orcid.org/0000-0002-2047-2297</orcidid><orcidid>https://orcid.org/0000-0002-7847-8456</orcidid><orcidid>https://orcid.org/0000-0002-9670-7961</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Bioluminescence Cysts Cytokines Endometriosis Experiments Flow cytometry Genetic engineering Granulocytes Growth Gynecological diseases Immunohistochemistry Lymphocytes Menstruation Physiology Transgenic animals Ultrasonic imaging Uterus |
title | The Presence of Pre-Existing Endometriotic Lesions Promotes the Growth of New Lesions in the Peritoneal Cavity |
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