TY - JOUR
T1 - Messages from the Small Intestine Carried by Extracellular Vesicles in Prediabetes
T2 - A Proteomic Portrait
AU - Ferreira, Inês
AU - Machado de Oliveira, Rita
AU - Carvalho, Ana Sofia
AU - Teshima, Akiko
AU - Beck, Hans Christian
AU - Matthiesen, Rune
AU - Costa-Silva, Bruno
AU - Macedo, Maria Paula
N1 - Funding Information:
This work was supported by the Fundação para a Ciência e Tecnologia (grant no. PTDC/MEC-MET/29314/2017), iNOVA4Health UIDB/Multi/04462/2020, and Programa Gilead GÉNESE─Edição de 2019 awarded to M.P.M., R.M.O., and B.C.-S. I.F. is a recipient of Fundação para a Ciência e Tecnologia fellowship (PD/BD/114044/2015). A.T. is a recipient of the European Foundation for the Study of Diabetes and Japanese Diabetes Society Reciprocal Travel Research Fellowship Programme.
Publisher Copyright:
© 2022 The Authors. Published by American Chemical Society.
PY - 2022/4/1
Y1 - 2022/4/1
N2 - Extracellular vesicles (EVs) mediate communication in physiological and pathological conditions. In the pathogenesis of type 2 diabetes, inter-organ communication plays an important role in its progress and metabolic surgery leads to its remission. Moreover, gut dysbiosis is emerging as a diabetogenic factor. However, it remains unclear how the gut senses metabolic alterations and whether this is transmitted to other tissues via EVs. Using a diet-induced prediabetic mouse model, we observed that protein packaging in gut-derived EVs (GDE), specifically the small intestine, is altered in prediabetes. Proteins related to lipid metabolism and to oxidative stress management were more abundant in prediabetic GDE compared to healthy controls. On the other hand, proteins related to glycolytic activity, as well as those responsible for the degradation of polyubiquitinated composites, were depleted in prediabetic GDE. Together, our findings show that protein packaging in GDE is markedly modified during prediabetes pathogenesis, thus suggesting that prediabetic alterations in the small intestine are translated into modified GDE proteomes, which are dispersed into the circulation where they can interact with and influence the metabolic status of other tissues. This study highlights the importance of the small intestine as a tissue that propagates prediabetic metabolic dysfunction throughout the body and the importance of GDE as the messengers. Data are available via ProteomeXchange with identifier PXD028338.
AB - Extracellular vesicles (EVs) mediate communication in physiological and pathological conditions. In the pathogenesis of type 2 diabetes, inter-organ communication plays an important role in its progress and metabolic surgery leads to its remission. Moreover, gut dysbiosis is emerging as a diabetogenic factor. However, it remains unclear how the gut senses metabolic alterations and whether this is transmitted to other tissues via EVs. Using a diet-induced prediabetic mouse model, we observed that protein packaging in gut-derived EVs (GDE), specifically the small intestine, is altered in prediabetes. Proteins related to lipid metabolism and to oxidative stress management were more abundant in prediabetic GDE compared to healthy controls. On the other hand, proteins related to glycolytic activity, as well as those responsible for the degradation of polyubiquitinated composites, were depleted in prediabetic GDE. Together, our findings show that protein packaging in GDE is markedly modified during prediabetes pathogenesis, thus suggesting that prediabetic alterations in the small intestine are translated into modified GDE proteomes, which are dispersed into the circulation where they can interact with and influence the metabolic status of other tissues. This study highlights the importance of the small intestine as a tissue that propagates prediabetic metabolic dysfunction throughout the body and the importance of GDE as the messengers. Data are available via ProteomeXchange with identifier PXD028338.
KW - diet
KW - extracellular vesicles
KW - lipids
KW - small intestines
KW - type 2 diabetes
UR - http://www.scopus.com/inward/record.url?scp=85126569526&partnerID=8YFLogxK
U2 - 10.1021/acs.jproteome.1c00353
DO - 10.1021/acs.jproteome.1c00353
M3 - Article
C2 - 35263542
AN - SCOPUS:85126569526
SN - 1535-3893
JO - Journal Of Proteome Research
JF - Journal Of Proteome Research
ER -