Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting

Detalhes bibliográficos
Autor(a) principal: Pereira, Ana Raquel Santos
Data de Publicação: 2022
Tipo de documento: Dissertação
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/131417
Resumo: African trypanosomiasis is a vector-borne disease caused by extracellular protozoan parasites, including Trypanosoma brucei. The establishment of infection in mammalian hosts is characterized by invasion of the bloodstream and solid tissues. Among these, the adipose tissue (AT) is heavily colonized by T. brucei in mice. During infection there is also a large reduction of AT mass which suggests the mobilization of lipids stored in the adipocyte. However, it is not known how adipocyte to parasite interactions may contribute to adipocyte lipid metabolism. Here we show that co-culturing 3T3-L1 adipocytes and T. brucei in vitro increased adipocyte lipolysis. We found that this increase can be elicited by a soluble parasite factor, but it is larger when live parasites are in direct contact with adipocytes. Furthermore, chemical inhibition of adipose triglyceride lipase (ATGL) during co-culture lead to a reduction of fatty acid and glycerol release, indicating that the release of lipolytic products in the presence of T. brucei is an ATGL-dependent mechanism. Overall, the findings in this study indicate that T. brucei is able to directly modulate adipocyte catabolism, highlighting the need to further investigate the molecular partners involved in this host-parasite interaction.
id RCAP_f48f32e80ba29938b65bd8f61d6c6f88
oai_identifier_str oai:run.unl.pt:10362/131417
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Adipocyte metabolic response to Trypanosoma brucei in a co-culture settingTrypanosoma bruceiadipose tissuelipolysis3T3-L1 adipocyteDomínio/Área Científica::Ciências Médicas::Outras Ciências MédicasAfrican trypanosomiasis is a vector-borne disease caused by extracellular protozoan parasites, including Trypanosoma brucei. The establishment of infection in mammalian hosts is characterized by invasion of the bloodstream and solid tissues. Among these, the adipose tissue (AT) is heavily colonized by T. brucei in mice. During infection there is also a large reduction of AT mass which suggests the mobilization of lipids stored in the adipocyte. However, it is not known how adipocyte to parasite interactions may contribute to adipocyte lipid metabolism. Here we show that co-culturing 3T3-L1 adipocytes and T. brucei in vitro increased adipocyte lipolysis. We found that this increase can be elicited by a soluble parasite factor, but it is larger when live parasites are in direct contact with adipocytes. Furthermore, chemical inhibition of adipose triglyceride lipase (ATGL) during co-culture lead to a reduction of fatty acid and glycerol release, indicating that the release of lipolytic products in the presence of T. brucei is an ATGL-dependent mechanism. Overall, the findings in this study indicate that T. brucei is able to directly modulate adipocyte catabolism, highlighting the need to further investigate the molecular partners involved in this host-parasite interaction.A tripanossomíase africana é uma doença transmitida por vetores, causada por parasitas protozoários extracelulares, incluindo o Trypanosoma brucei. A infeção do hospedeiro mamífero caracteriza-se pela invasão do sistema circulatório e de outros tecidos. Entre estes encontra-se o tecido adiposo, que é extensamente colonizado por T. brucei em ratinho. Durante a infeção ocorre uma grande redução da massa do tecido adiposo, sugerindo existir mobilização de lípidos armazenados no adipócito. Contudo, não é conhecido como a interação entre o parasita e o adipócito poderá contribuir para o metabolismo de lípidos no adipócito. Neste estudo demonstramos que num sistema in vitro de co-cultura com adipócitos 3T3-L1 e T. brucei existe um aumento da lipólise no adipócito. Este aumento pode ser despoletado por um fator solúvel com origem no parasita, no entanto o seu efeito é máximo quando o parasita está viável e em contato direto com o adipócito. Adicionalmente, a inibição química da ATGL durante a co-cultura resulta numa redução da libertação de ácidos gordos e glicerol, indicando que a lipólise induzida por T. brucei é dependente da atividade da ATGL. Globalmente, os resultados deste estudo indicam que o T. brucei pode modular diretamente o catabolismo do adipócito, realçando a necessidade de investigar os mediadores moleculares envolvidos na interação entre hospedeiro e parasita.Figueiredo, LuísaRUNPereira, Ana Raquel Santos2022-01-212024-11-01T00:00:00Z2022-01-21T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10362/131417enginfo:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T05:10:00Zoai:run.unl.pt:10362/131417Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:47:03.692890Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting
title Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting
spellingShingle Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting
Pereira, Ana Raquel Santos
Trypanosoma brucei
adipose tissue
lipolysis
3T3-L1 adipocyte
Domínio/Área Científica::Ciências Médicas::Outras Ciências Médicas
title_short Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting
title_full Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting
title_fullStr Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting
title_full_unstemmed Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting
title_sort Adipocyte metabolic response to Trypanosoma brucei in a co-culture setting
author Pereira, Ana Raquel Santos
author_facet Pereira, Ana Raquel Santos
author_role author
dc.contributor.none.fl_str_mv Figueiredo, Luísa
RUN
dc.contributor.author.fl_str_mv Pereira, Ana Raquel Santos
dc.subject.por.fl_str_mv Trypanosoma brucei
adipose tissue
lipolysis
3T3-L1 adipocyte
Domínio/Área Científica::Ciências Médicas::Outras Ciências Médicas
topic Trypanosoma brucei
adipose tissue
lipolysis
3T3-L1 adipocyte
Domínio/Área Científica::Ciências Médicas::Outras Ciências Médicas
description African trypanosomiasis is a vector-borne disease caused by extracellular protozoan parasites, including Trypanosoma brucei. The establishment of infection in mammalian hosts is characterized by invasion of the bloodstream and solid tissues. Among these, the adipose tissue (AT) is heavily colonized by T. brucei in mice. During infection there is also a large reduction of AT mass which suggests the mobilization of lipids stored in the adipocyte. However, it is not known how adipocyte to parasite interactions may contribute to adipocyte lipid metabolism. Here we show that co-culturing 3T3-L1 adipocytes and T. brucei in vitro increased adipocyte lipolysis. We found that this increase can be elicited by a soluble parasite factor, but it is larger when live parasites are in direct contact with adipocytes. Furthermore, chemical inhibition of adipose triglyceride lipase (ATGL) during co-culture lead to a reduction of fatty acid and glycerol release, indicating that the release of lipolytic products in the presence of T. brucei is an ATGL-dependent mechanism. Overall, the findings in this study indicate that T. brucei is able to directly modulate adipocyte catabolism, highlighting the need to further investigate the molecular partners involved in this host-parasite interaction.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-21
2022-01-21T00:00:00Z
2024-11-01T00:00:00Z
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 http://hdl.handle.net/10362/131417
url http://hdl.handle.net/10362/131417
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/embargoedAccess
eu_rights_str_mv embargoedAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799138073928269824