Bio-Distribution of Pancreas-Derived Exosomes

Bibliographic Details
Main Author: Sara Raquel Sousa Alves
Publication Date: 2024
Format: Master thesis
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/10216/163924
Summary: Exosomes, a subtype of extracellular vesicles (EVs), are nanoparticles released by all cell types that play a crucial role in intercellular communication. Despite their importance in both pathological and non-pathological processes, the dynamics of exosomes within living systems remain poorly understood. Pancreatic ductal adenocarcinoma (PDAC), a highly lethal disease with a 5-year survival rate of only 13%, has been shown to involve EVs in its establishment, maintenance, and progression. In this thesis, a genetically engineered mouse model (ExoBow) was used to map the spatiotemporal biodistribution of pancreas-derived exosomes in both non pathological and PDAC-affected mice. It was successfully confirmed the size, identity, and purity of exosomes secreted by PDAC cell lines transfected with the ExoBow transgene. However, ex vivo analysis of mouse PDAC cell lines revealed variability in exosome secretion rates, likely reflecting tumor heterogeneity. As PDAC progressed, a gradual increase in the intensity and quantity of pancreas-derived exosome communication was observed, with fluctuations in exosome distribution in non-pathological contexts in 8-, 17-, and 30-week-old mice. In healthy mice, pancreas-derived exosomes exhibited organotropism, preferentially targeting immune organs such as the thymus at 8 weeks and the spleen at 30 weeks. Using another GEMM designed to block exosome secretion, it was found that the absence of exosomes did not affect the structural integrity of the thymus at 17 weeks. The development of this novel GEMM allows for the endogenous mapping of exosome secretion, providing new insights into how exosome production is influenced by age, homeostatic or disease stage. This information is significant for the advancement in the field of EV research and offers a valuable tool for further exploration of exosome-mediated communication.
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spelling Bio-Distribution of Pancreas-Derived ExosomesCiências médicas e da saúdeMedical and Health sciencesExosomes, a subtype of extracellular vesicles (EVs), are nanoparticles released by all cell types that play a crucial role in intercellular communication. Despite their importance in both pathological and non-pathological processes, the dynamics of exosomes within living systems remain poorly understood. Pancreatic ductal adenocarcinoma (PDAC), a highly lethal disease with a 5-year survival rate of only 13%, has been shown to involve EVs in its establishment, maintenance, and progression. In this thesis, a genetically engineered mouse model (ExoBow) was used to map the spatiotemporal biodistribution of pancreas-derived exosomes in both non pathological and PDAC-affected mice. It was successfully confirmed the size, identity, and purity of exosomes secreted by PDAC cell lines transfected with the ExoBow transgene. However, ex vivo analysis of mouse PDAC cell lines revealed variability in exosome secretion rates, likely reflecting tumor heterogeneity. As PDAC progressed, a gradual increase in the intensity and quantity of pancreas-derived exosome communication was observed, with fluctuations in exosome distribution in non-pathological contexts in 8-, 17-, and 30-week-old mice. In healthy mice, pancreas-derived exosomes exhibited organotropism, preferentially targeting immune organs such as the thymus at 8 weeks and the spleen at 30 weeks. Using another GEMM designed to block exosome secretion, it was found that the absence of exosomes did not affect the structural integrity of the thymus at 17 weeks. The development of this novel GEMM allows for the endogenous mapping of exosome secretion, providing new insights into how exosome production is influenced by age, homeostatic or disease stage. This information is significant for the advancement in the field of EV research and offers a valuable tool for further exploration of exosome-mediated communication.2024-12-092024-12-09T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttps://hdl.handle.net/10216/163924TID:203753321engSara Raquel Sousa Alvesinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-27T19:15:27Zoai:repositorio-aberto.up.pt:10216/163924Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T23:12:38.887910Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Bio-Distribution of Pancreas-Derived Exosomes
title Bio-Distribution of Pancreas-Derived Exosomes
spellingShingle Bio-Distribution of Pancreas-Derived Exosomes
Sara Raquel Sousa Alves
Ciências médicas e da saúde
Medical and Health sciences
title_short Bio-Distribution of Pancreas-Derived Exosomes
title_full Bio-Distribution of Pancreas-Derived Exosomes
title_fullStr Bio-Distribution of Pancreas-Derived Exosomes
title_full_unstemmed Bio-Distribution of Pancreas-Derived Exosomes
title_sort Bio-Distribution of Pancreas-Derived Exosomes
author Sara Raquel Sousa Alves
author_facet Sara Raquel Sousa Alves
author_role author
dc.contributor.author.fl_str_mv Sara Raquel Sousa Alves
dc.subject.por.fl_str_mv Ciências médicas e da saúde
Medical and Health sciences
topic Ciências médicas e da saúde
Medical and Health sciences
description Exosomes, a subtype of extracellular vesicles (EVs), are nanoparticles released by all cell types that play a crucial role in intercellular communication. Despite their importance in both pathological and non-pathological processes, the dynamics of exosomes within living systems remain poorly understood. Pancreatic ductal adenocarcinoma (PDAC), a highly lethal disease with a 5-year survival rate of only 13%, has been shown to involve EVs in its establishment, maintenance, and progression. In this thesis, a genetically engineered mouse model (ExoBow) was used to map the spatiotemporal biodistribution of pancreas-derived exosomes in both non pathological and PDAC-affected mice. It was successfully confirmed the size, identity, and purity of exosomes secreted by PDAC cell lines transfected with the ExoBow transgene. However, ex vivo analysis of mouse PDAC cell lines revealed variability in exosome secretion rates, likely reflecting tumor heterogeneity. As PDAC progressed, a gradual increase in the intensity and quantity of pancreas-derived exosome communication was observed, with fluctuations in exosome distribution in non-pathological contexts in 8-, 17-, and 30-week-old mice. In healthy mice, pancreas-derived exosomes exhibited organotropism, preferentially targeting immune organs such as the thymus at 8 weeks and the spleen at 30 weeks. Using another GEMM designed to block exosome secretion, it was found that the absence of exosomes did not affect the structural integrity of the thymus at 17 weeks. The development of this novel GEMM allows for the endogenous mapping of exosome secretion, providing new insights into how exosome production is influenced by age, homeostatic or disease stage. This information is significant for the advancement in the field of EV research and offers a valuable tool for further exploration of exosome-mediated communication.
publishDate 2024
dc.date.none.fl_str_mv 2024-12-09
2024-12-09T00:00:00Z
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