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Adipose Tissue-Derived Signatures for Obesity and Type 2 Diabetes: Adipokines, Batokines and MicroRNAs

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dc.contributor.authorLee, Min-Woo-
dc.contributor.authorLee, Mihye-
dc.contributor.authorOh, Kyoung-Jin-
dc.date.accessioned2021-08-11T09:43:52Z-
dc.date.available2021-08-11T09:43:52Z-
dc.date.issued2019-06-
dc.identifier.issn2077-0383-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/4481-
dc.description.abstractObesity is one of the main risk factors for type 2 diabetes mellitus (T2DM). It is closely related to metabolic disturbances in the adipose tissue that primarily functions as a fat reservoir. For this reason, adipose tissue is considered as the primary site for initiation and aggravation of obesity and T2DM. As a key endocrine organ, the adipose tissue communicates with other organs, such as the brain, liver, muscle, and pancreas, for the maintenance of energy homeostasis. Two different types of adipose tissues-the white adipose tissue (WAT) and brown adipose tissue (BAT)-secrete bioactive peptides and proteins, known as adipokines and batokines, respectively. Some of them have beneficial anti-inflammatory effects, while others have harmful inflammatory effects. Recently, exosomal microRNAs (miRNAs) were identified as novel adipokines, as adipose tissue-derived exosomal miRNAs can affect other organs. In the present review, we discuss the role of adipose-derived secretory factors-adipokines, batokines, and exosomal miRNA-in obesity and T2DM. It will provide new insights into the pathophysiological mechanisms involved in disturbances of adipose-derived factors and will support the development of adipose-derived factors as potential therapeutic targets for obesity and T2DM.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI AG-
dc.titleAdipose Tissue-Derived Signatures for Obesity and Type 2 Diabetes: Adipokines, Batokines and MicroRNAs-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/jcm8060854-
dc.identifier.wosid000475349300098-
dc.identifier.bibliographicCitationJournal of Clinical Medicine, v.8, no.6-
dc.citation.titleJournal of Clinical Medicine-
dc.citation.volume8-
dc.citation.number6-
dc.type.docTypeReview-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.subject.keywordPlusACYLATION-STIMULATING PROTEIN-
dc.subject.keywordPlusACID-BINDING PROTEIN-
dc.subject.keywordPlusBONE MORPHOGENETIC PROTEIN-7-
dc.subject.keywordPlusFIBROBLAST GROWTH FACTOR-21-
dc.subject.keywordPlusREGULATES INSULIN-SECRETION-
dc.subject.keywordPlusSERUM VASPIN CONCENTRATIONS-
dc.subject.keywordPlusANGIOPOIETIN-LIKE PROTEIN-
dc.subject.keywordPlusANTIGEN-PRESENTING CELLS-
dc.subject.keywordPlusPROSTAGLANDIN D SYNTHASE-
dc.subject.keywordPlusHIGH-FAT DIET-
dc.subject.keywordAuthorobesity-
dc.subject.keywordAuthortype 2 diabetes mellitus-
dc.subject.keywordAuthoradipokines-
dc.subject.keywordAuthorbatokines-
dc.subject.keywordAuthorexosomal miRNAs-
dc.subject.keywordAuthorpotential therapeutic targets-
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