Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication
| Ano de defesa: | 2024 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | |
| Tipo de documento: | Dissertação |
| Tipo de acesso: | Acesso aberto |
| Idioma: | eng |
| Instituição de defesa: |
Biblioteca Digitais de Teses e Dissertações da USP
|
| Programa de Pós-Graduação: |
Não Informado pela instituição
|
| Departamento: |
Não Informado pela instituição
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| País: |
Não Informado pela instituição
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| Palavras-chave em Português: | |
| Link de acesso: | https://www.teses.usp.br/teses/disponiveis/10/10132/tde-01102024-173813/ |
Resumo: | In cattle, high rates of embryonic losses are significant, with approximately 10% attributed to fertilization failures and 50% to embryonic developmental issues. To better understand these processes, we employed 3D culture to simulate the in vivo endometrial environment. Our study developed an in vitro setting using endometrial gland organoids co-cultured with epithelial and stromal cells (GES), investigating how this communication affects interaction with bovine embryos. We hypothesized that this 3D model mimics conditions closer to the in vivo bovine uterus. The study was divided into two experiments. In Experiment 1, we assessed the morphological effects of glandular organoids and GES under varying progesterone concentrations from D2 to D9. We observed initial variability in the growth of endometrial glands, regardless of hormonal exposure initiated on D2. Effects of hormonal treatments (E2, P4, E2+P4) on organoid height and area on D9 were noted. In both groups (isolated glands and GES), treatments with P4 and E2+P4 resulted in larger spherical areas compared to control. In Experiment 2, we investigated the combined effect of E2+P4 in the Gland versus GES groups, introducing embryos on day 7 of development and evaluating on day 8 of culture. We focused on 382 microRNAs (miRNAs), analyzing their profiles in Gland_CT, Gland_E2+P4, Gland_E2+P4_Emb, GES_CT, GES_E2+P4, and GES_Emb_E2+P4 groups. Unique miRNAs were identified in each group, with bioinformatic analyses predicting modulation of various biological pathways. The Axon Guidance pathway was common across all Gland groups, underscoring its significance. In the GES group, we identified 12 unique miRNAs in GES_CT, 2 in GES_E2+ P4, and 12 in GES_Emb_E2+P4, modulating pathways such as oxytocin signaling and mTOR signaling, among others. The “Pathway in Cancer” was common among subgroups, associated with multiple biological functions. These findings highlight the complexity of regulatory interactions in 3D culture models for studying maternal-embryonic communication in cattle. Co-cultivating glands with epithelial and stromal cells to create an environment mimicking the bovine endometrium in vitro for studying maternal-embryonic communication proved to be a promising model aligned with study expectations. |
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Biblioteca Digital de Teses e Dissertações da USP |
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Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communicationEstabelecimento do cultivo in vitro de organoides endometrial bovinos para estudo da comunicação materna embrionária3D cultureComunicação materno-embrionáriaCultivo 3DEndometrial organoidsMaternal-embryonic communicationmiRNAsmiRNAsOrganoides endometriaisSignaling pathwaysVias de sinalizaçãoIn cattle, high rates of embryonic losses are significant, with approximately 10% attributed to fertilization failures and 50% to embryonic developmental issues. To better understand these processes, we employed 3D culture to simulate the in vivo endometrial environment. Our study developed an in vitro setting using endometrial gland organoids co-cultured with epithelial and stromal cells (GES), investigating how this communication affects interaction with bovine embryos. We hypothesized that this 3D model mimics conditions closer to the in vivo bovine uterus. The study was divided into two experiments. In Experiment 1, we assessed the morphological effects of glandular organoids and GES under varying progesterone concentrations from D2 to D9. We observed initial variability in the growth of endometrial glands, regardless of hormonal exposure initiated on D2. Effects of hormonal treatments (E2, P4, E2+P4) on organoid height and area on D9 were noted. In both groups (isolated glands and GES), treatments with P4 and E2+P4 resulted in larger spherical areas compared to control. In Experiment 2, we investigated the combined effect of E2+P4 in the Gland versus GES groups, introducing embryos on day 7 of development and evaluating on day 8 of culture. We focused on 382 microRNAs (miRNAs), analyzing their profiles in Gland_CT, Gland_E2+P4, Gland_E2+P4_Emb, GES_CT, GES_E2+P4, and GES_Emb_E2+P4 groups. Unique miRNAs were identified in each group, with bioinformatic analyses predicting modulation of various biological pathways. The Axon Guidance pathway was common across all Gland groups, underscoring its significance. In the GES group, we identified 12 unique miRNAs in GES_CT, 2 in GES_E2+ P4, and 12 in GES_Emb_E2+P4, modulating pathways such as oxytocin signaling and mTOR signaling, among others. The “Pathway in Cancer” was common among subgroups, associated with multiple biological functions. These findings highlight the complexity of regulatory interactions in 3D culture models for studying maternal-embryonic communication in cattle. Co-cultivating glands with epithelial and stromal cells to create an environment mimicking the bovine endometrium in vitro for studying maternal-embryonic communication proved to be a promising model aligned with study expectations.Em vacas, altas taxas de perdas embrionárias se tornam relevantes, com cerca de 10% devido a falhas na fertilização e 50% devido a falhas no desenvolvimento embrionário. Para entender melhor esses processos, utilizamos cultivo 3D para simular o ambiente endometrial in vivo. Nosso estudo desenvolve um ambiente in vitro usando esferoides de glândulas endometriais co-cultivados com células epiteliais e estromais (GES), investigando como essa comunicação afeta a interação com embriões bovinos. Hipotetizamos que esse modelo 3D mimetiza condições mais próximas do útero in vivo em bovinos. Dividimos o estudo em dois experimentos. No Experimento 1, avaliamos os efeitos morfológicos dos esferoides glandulares e GES sob diferentes concentrações de progesterona, de D2 a D9. Observamos uma variabilidade inicial no crescimento das glândulas endometriais, independentemente da exposição hormonal iniciada no D2. Os efeitos dos tratamentos hormonais (E2, P4, E2+P4) na altura e área dos esferoides no D9. Constatamos que, em ambos os grupos (glândulas isoladas e GES), os tratamentos com P4 e E2+P4 resultaram em áreas esféricas maiores em comparação ao controle. No Experimento 2, investigamos o efeito da combinação de E2+P4 no grupo Gland versus GES, introduzindo embriões no dia 7 do desenvolvimento e avaliando no dia 8 do cultivo. Focamos em 382 microRNAs (miRNAs), analisando seus perfis nos grupos Gland_CT, Gland_E2+P4, Gland_E2+P4_Emb, GES_CT, GES_E2+P4, e GES_Emb_E2+P4. Identificamos miRNAs exclusivos em cada grupo, com análises bioinformáticas prevendo a modulação de diversas vias biológicas. Destacamos que a via Axon Guidance foi comum a todos os grupos Gland, mostrando sua importância. No grupo GES, identificamos 12 miRNAs exclusivos em GES_CT, 2 em GES_E2+P4, e 12 em GES_Emb_E2+P4, modulando diferentes vias como sinalização de oxitocina, e sinalização de mTOR, entre outras. A via “Pathway in Cancer” foi comum entre os subgrupos, associada a múltiplas funções biológicas. Esses resultados destacam a complexidade das interações regulatórias nos modelos de cultura 3D para estudo da comunicação materno-embrionária em bovinos. O uso de glândulas cocultivadas com células epiteliais e estromais para gerar um ambiente que mimetize o endométrio bovino in vitro para estudar a comunicação materno-embrionária apresentou-se como um modelo que corresponde às expectativas do estudo.Biblioteca Digitais de Teses e Dissertações da USPBem, Tiago Henrique Camara deMeirelles, Flavio VieiraOshiro, Thais Sayuri Imura2024-07-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttps://www.teses.usp.br/teses/disponiveis/10/10132/tde-01102024-173813/reponame:Biblioteca Digital de Teses e Dissertações da USPinstname:Universidade de São Paulo (USP)instacron:USPLiberar o conteúdo para acesso público.info:eu-repo/semantics/openAccesseng2024-12-09T15:19:02Zoai:teses.usp.br:tde-01102024-173813Biblioteca Digital de Teses e Dissertaçõeshttp://www.teses.usp.br/PUBhttp://www.teses.usp.br/cgi-bin/mtd2br.plvirginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.bropendoar:27212024-12-09T15:19:02Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)false |
| dc.title.none.fl_str_mv |
Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication Estabelecimento do cultivo in vitro de organoides endometrial bovinos para estudo da comunicação materna embrionária |
| title |
Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication |
| spellingShingle |
Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication Oshiro, Thais Sayuri Imura 3D culture Comunicação materno-embrionária Cultivo 3D Endometrial organoids Maternal-embryonic communication miRNAs miRNAs Organoides endometriais Signaling pathways Vias de sinalização |
| title_short |
Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication |
| title_full |
Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication |
| title_fullStr |
Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication |
| title_full_unstemmed |
Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication |
| title_sort |
Establishment of in vitro culture of bovine endometrial organoids for the study of maternal-embryonic communication |
| author |
Oshiro, Thais Sayuri Imura |
| author_facet |
Oshiro, Thais Sayuri Imura |
| author_role |
author |
| dc.contributor.none.fl_str_mv |
Bem, Tiago Henrique Camara de Meirelles, Flavio Vieira |
| dc.contributor.author.fl_str_mv |
Oshiro, Thais Sayuri Imura |
| dc.subject.por.fl_str_mv |
3D culture Comunicação materno-embrionária Cultivo 3D Endometrial organoids Maternal-embryonic communication miRNAs miRNAs Organoides endometriais Signaling pathways Vias de sinalização |
| topic |
3D culture Comunicação materno-embrionária Cultivo 3D Endometrial organoids Maternal-embryonic communication miRNAs miRNAs Organoides endometriais Signaling pathways Vias de sinalização |
| description |
In cattle, high rates of embryonic losses are significant, with approximately 10% attributed to fertilization failures and 50% to embryonic developmental issues. To better understand these processes, we employed 3D culture to simulate the in vivo endometrial environment. Our study developed an in vitro setting using endometrial gland organoids co-cultured with epithelial and stromal cells (GES), investigating how this communication affects interaction with bovine embryos. We hypothesized that this 3D model mimics conditions closer to the in vivo bovine uterus. The study was divided into two experiments. In Experiment 1, we assessed the morphological effects of glandular organoids and GES under varying progesterone concentrations from D2 to D9. We observed initial variability in the growth of endometrial glands, regardless of hormonal exposure initiated on D2. Effects of hormonal treatments (E2, P4, E2+P4) on organoid height and area on D9 were noted. In both groups (isolated glands and GES), treatments with P4 and E2+P4 resulted in larger spherical areas compared to control. In Experiment 2, we investigated the combined effect of E2+P4 in the Gland versus GES groups, introducing embryos on day 7 of development and evaluating on day 8 of culture. We focused on 382 microRNAs (miRNAs), analyzing their profiles in Gland_CT, Gland_E2+P4, Gland_E2+P4_Emb, GES_CT, GES_E2+P4, and GES_Emb_E2+P4 groups. Unique miRNAs were identified in each group, with bioinformatic analyses predicting modulation of various biological pathways. The Axon Guidance pathway was common across all Gland groups, underscoring its significance. In the GES group, we identified 12 unique miRNAs in GES_CT, 2 in GES_E2+ P4, and 12 in GES_Emb_E2+P4, modulating pathways such as oxytocin signaling and mTOR signaling, among others. The “Pathway in Cancer” was common among subgroups, associated with multiple biological functions. These findings highlight the complexity of regulatory interactions in 3D culture models for studying maternal-embryonic communication in cattle. Co-cultivating glands with epithelial and stromal cells to create an environment mimicking the bovine endometrium in vitro for studying maternal-embryonic communication proved to be a promising model aligned with study expectations. |
| publishDate |
2024 |
| dc.date.none.fl_str_mv |
2024-07-30 |
| dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
| dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
| format |
masterThesis |
| status_str |
publishedVersion |
| dc.identifier.uri.fl_str_mv |
https://www.teses.usp.br/teses/disponiveis/10/10132/tde-01102024-173813/ |
| url |
https://www.teses.usp.br/teses/disponiveis/10/10132/tde-01102024-173813/ |
| dc.language.iso.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
|
| dc.rights.driver.fl_str_mv |
Liberar o conteúdo para acesso público. info:eu-repo/semantics/openAccess |
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Liberar o conteúdo para acesso público. |
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openAccess |
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application/pdf |
| dc.coverage.none.fl_str_mv |
|
| dc.publisher.none.fl_str_mv |
Biblioteca Digitais de Teses e Dissertações da USP |
| publisher.none.fl_str_mv |
Biblioteca Digitais de Teses e Dissertações da USP |
| dc.source.none.fl_str_mv |
reponame:Biblioteca Digital de Teses e Dissertações da USP instname:Universidade de São Paulo (USP) instacron:USP |
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Universidade de São Paulo (USP) |
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USP |
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USP |
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Biblioteca Digital de Teses e Dissertações da USP |
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Biblioteca Digital de Teses e Dissertações da USP |
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Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP) |
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virginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.br |
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1865490633710370816 |