Exosomes and diabetes

被引:92
作者
Castano, Carlos [1 ,2 ]
Novials, Anna [1 ,2 ]
Parrizas, Marcelina [1 ,2 ]
机构
[1] Inst Invest Biomed August Pi & Sunyer IDIBAPS, Diabet & Obes Res Lab, Barcelona, Spain
[2] Spanish Biomed Res Ctr Diabet & Associated Metab, Barcelona, Spain
关键词
crosstalk; diabetes; exosome; microRNA; obesity; therapy; MESENCHYMAL STEM-CELLS; INSULINOMA-RELEASED EXOSOMES; MACROPHAGE POLARIZATION; EXTRACELLULAR VESICLES; CIRCULATING MICRORNAS; GENE-EXPRESSION; ADIPOSE-TISSUE; IN-VIVO; CANCER; RESISTANCE;
D O I
10.1002/dmrr.3107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes is a group of metabolic diseases characterized by elevated blood glucose levels that drive the development of life-threatening complications. Diabetes results from a situation of insufficient insulin action, either by deficient production of the hormone by the pancreas, or by the development of insulin resistance in peripheral tissues such as liver, muscle, or the adipose depots. Communication between organs is thus central to the maintenance of glucose homoeostasis. Recently, several studies are evidencing that small vesicles called exosomes released by, amongst other, the adipose tissue can regulate gene expression in other tissues, hence modulating interorgan crosstalk. Therefore, exosomes participate in the development of diabetes and its associated complications. Their study holds the potential of providing us with novel biomarkers for the early diagnosis and stratification of patients at risk of developing diabetes, hence allowing the timely implementation of more personalized therapies. On the other hand, the molecular dissection of the pathways initiated by exosomes under situations of metabolic stress could help to gain a deeper knowledge of the pathophysiology of diabetes and its associated metabolic diseases.
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页数:10
相关论文
共 101 条
[31]   Early-Life Exposures and Risk of Diabetes Mellitus and Obesity [J].
Gingras, Veronique ;
Hivert, Marie-France ;
Oken, Emily .
CURRENT DIABETES REPORTS, 2018, 18 (10)
[32]   Lymphocyte-Derived Exosomal MicroRNAs Promote Pancreatic β Cell Death and May Contribute to Type 1 Diabetes Development [J].
Guay, Claudiane ;
Kruit, Janine K. ;
Rome, Sophie ;
Menoud, Veronique ;
Mulder, Niels L. ;
Jurdzinski, Angelika ;
Mancarella, Francesca ;
Sebastiani, Guido ;
Donda, Alena ;
Gonzalez, Bryan J. ;
Jandus, Camilla ;
Bouzakri, Karim ;
Pinget, Michel ;
Boitard, Christian ;
Romero, Pedro ;
Dotta, Francesco ;
Regazzi, Romano .
CELL METABOLISM, 2019, 29 (02) :348-+
[33]   Exosomes as new players in metabolic organ cross-talk [J].
Guay, Claudiane ;
Regazzi, Romano .
DIABETES OBESITY & METABOLISM, 2017, 19 :137-146
[34]   Horizontal transfer of exosomal microRNAs transduce apoptotic signals between pancreatic beta-cells [J].
Guay, Claudiane ;
Menoud, Veronique ;
Rome, Sophie ;
Regazzi, Romano .
CELL COMMUNICATION AND SIGNALING, 2015, 13
[35]   Atheroprotective communication between endothelial cells and smooth muscle cells through miRNAs [J].
Hergenreider, Eduard ;
Heydt, Susanne ;
Treguer, Karine ;
Boettger, Thomas ;
Horrevoets, Anton J. G. ;
Zeiher, Andreas M. ;
Scheffer, Margot P. ;
Frangakis, Achilleas S. ;
Yin, Xiaoke ;
Mayr, Manuel ;
Braun, Thomas ;
Urbich, Carmen ;
Boon, Reinier A. ;
Dimmeler, Stefanie .
NATURE CELL BIOLOGY, 2012, 14 (03) :249-+
[36]   Tumour exosome integrins determine organotropic metastasis [J].
Hoshino, Ayuko ;
Costa-Silva, Bruno ;
Shen, Tang-Long ;
Rodrigues, Goncalo ;
Hashimoto, Ayako ;
Mark, Milica Tesic ;
Molina, Henrik ;
Kohsaka, Shinji ;
Di Giannatale, Angela ;
Ceder, Sophia ;
Singh, Swarnima ;
Williams, Caitlin ;
Soplop, Nadine ;
Uryu, Kunihiro ;
Pharmer, Lindsay ;
King, Tari ;
Bojmar, Linda ;
Davies, Alexander E. ;
Ararso, Yonathan ;
Zhang, Tuo ;
Zhang, Haiying ;
Hernandez, Jonathan ;
Weiss, Joshua M. ;
Dumont-Cole, Vanessa D. ;
Kramer, Kimberly ;
Wexler, Leonard H. ;
Narendran, Aru ;
Schwartz, Gary K. ;
Healey, John H. ;
Sandstrom, Per ;
Labori, Knut Jorgen ;
Kure, Elin H. ;
Grandgenett, Paul M. ;
Hollingsworth, Michael A. ;
de Sousa, Maria ;
Kaur, Sukhwinder ;
Jain, Maneesh ;
Mallya, Kavita ;
Batra, Surinder K. ;
Jarnagin, William R. ;
Brady, Mary S. ;
Fodstad, Oystein ;
Muller, Volkmar ;
Pantel, Klaus ;
Minn, Andy J. ;
Bissell, Mina J. ;
Garcia, Benjamin A. ;
Kang, Yibin ;
Rajasekhar, Vinagolu K. ;
Ghajar, Cyrus M. .
NATURE, 2015, 527 (7578) :329-+
[37]   Plasma Exosomes Contribute to Microvascular Damage in Diabetic Retinopathy by Activating the Classical Complement Pathway [J].
Huang, Chao ;
Fisher, Kiera P. ;
Hammer, Sandra S. ;
Navitskaya, Svetlana ;
Blanchard, Gary J. ;
Busik, Julia V. .
DIABETES, 2018, 67 (08) :1639-1649
[38]   Macrophage-dependent clearance of systemically administered B16BL6-derived exosomes from the blood circulation in mice [J].
Imai, Takafumi ;
Takahashi, Yuki ;
Nishikawa, Makiya ;
Kato, Kana ;
Morishita, Masaki ;
Yamashita, Takuma ;
Matsumoto, Akihiro ;
Charoenviriyakul, Chonlada ;
Takakura, Yoshinobu .
JOURNAL OF EXTRACELLULAR VESICLES, 2015, 4 :1-8
[39]  
International Diabetes Federation, 2017, Diabetes atlas
[40]   Exosome-like vesicles released from lipid-induced insulin-resistant muscles modulate gene expression and proliferation of beta recipient cells in mice [J].
Jalabert, Audrey ;
Vial, Guillaume ;
Guay, Claudiane ;
Wiklander, Oscar P. B. ;
Nordin, Joel Z. ;
Aswad, Hala ;
Forterre, Alexis ;
Meugnier, Emmanuelle ;
Pesenti, Sandra ;
Regazzi, Romano ;
Danty-Berger, Emmanuelle ;
Ducreux, Sylvie ;
Vidal, Hubert ;
El-Andaloussi, Samir ;
Rieusset, Jennifer ;
Rome, Sophie .
DIABETOLOGIA, 2016, 59 (05) :1049-1058