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      Dynamics of protein secretion during adipocyte differentiation

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          Abstract

          The major functions of adipocytes include both lipid storage and the production of secretory factors. However, the type of proteins released from mouse 3T3‐L1 cells during adipocyte differentiation remains poorly understood. We examined the dynamics of secreted proteins during adipocyte differentiation using mass spectrometry ( MS) combined with an iTRAQ ® labeling method that enables the simultaneous analysis of relative protein expression levels. A total of 215 proteins were identified and quantified from approximately 10 000 MS/ MS spectra. Of these, approximately 38% were categorized as secreted proteins based on gene ontology classification. Adipokine secretion levels were increased with the progression of differentiation. By contrast, levels of fibril collagen components, such as subunits of type I and III collagens, were decreased during differentiation. Basement membrane components attained their peak levels at day 4 when small lipid droplets accumulated in differentiated 3T3‐L1 cells. Simultaneously, peak levels of collagen microfibril components that comprise type V and VI collagen subunits were also observed. Our data demonstrated that extracellular matrix components were predominantly released during the early and middle stages of adipocyte differentiation, with a subsequent increase in the secretion of adipokines. This suggests that 3T3‐L1 cells secrete adipokines after their ECM is constructed during adipocyte differentiation.

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          Most cited references45

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          Metabolic dysregulation and adipose tissue fibrosis: role of collagen VI.

          Adipocytes are embedded in a unique extracellular matrix whose main function is to provide mechanical support, in addition to participating in a variety of signaling events. During adipose tissue expansion, the extracellular matrix requires remodeling to accommodate adipocyte growth. Here, we demonstrate a general upregulation of several extracellular matrix components in adipose tissue in the diabetic state, therefore implicating "adipose tissue fibrosis" as a hallmark of metabolically challenged adipocytes. Collagen VI is a highly enriched extracellular matrix component of adipose tissue. The absence of collagen VI results in the uninhibited expansion of individual adipocytes and is paradoxically associated with substantial improvements in whole-body energy homeostasis, both with high-fat diet exposure and in the ob/ob background. Collectively, our data suggest that weakening the extracellular scaffold of adipocytes enables their stress-free expansion during states of positive energy balance, which is consequently associated with an improved inflammatory profile. Therefore, the disproportionate accumulation of extracellular matrix components in adipose tissue may not be merely an epiphenomenon of metabolically challenging conditions but may also directly contribute to a failure to expand adipose tissue mass during states of excess caloric intake.
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            A novel serum protein similar to C1q, produced exclusively in adipocytes.

            We describe a novel 30-kDa secretory protein, Acrp30 (adipocyte complement-related protein of 30 kDa), that is made exclusively in adipocytes and whose mRNA is induced over 100-fold during adipocyte differentiation. Acrp30 is structurally similar to complement factor C1q and to a hibernation-specific protein isolated from the plasma of Siberian chipmunks; it forms large homo-oligomers that undergo a series of post-translational modifications. Like adipsin, secretion of Acrp30 is enhanced by insulin, and Acrp30 is an abundant serum protein. Acrp30 may be a factor that participates in the delicately balanced system of energy homeostasis involving food intake and carbohydrate and lipid catabolism. Our experiments also further corroborate the existence of an insulin-regulated secretory pathway in adipocytes.
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              cDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (AdiPose Most abundant Gene transcript 1).

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                Author and article information

                Journal
                FEBS Open Bio
                FEBS Open Bio
                10.1002/(ISSN)2211-5463
                FEB4
                FEBS Open Bio
                John Wiley and Sons Inc. (Hoboken )
                2211-5463
                15 June 2016
                August 2016
                : 6
                : 8 ( doiID: 10.1111/feb4.2016.6.issue-8 )
                : 816-826
                Affiliations
                [ 1 ] Animal Products Research DivisionNARO, Institute of Livestock and Grassland Science Tsukuba IbarakiJapan
                [ 2 ] Research Faculty of AgricultureHokkaido University Sapporo HokkaidoJapan
                Author notes
                [*] [* ] Correspondence

                K. Ojima, Animal Products Research Division, NARO, Institute of Livestock and Grassland Science, 2 Ikenodai, Tsukuba, Ibaraki 305‐0901, Japan

                Fax/Tel: +81 298 838 8686

                E‐mail: koojima@ 123456affrc.go.jp

                Article
                FEB412091
                10.1002/2211-5463.12091
                4971837
                27516960
                e96c748b-e436-4c29-b900-7bc2076dedde
                © 2016 The Authors. Published by FEBS Press and John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 04 February 2016
                : 25 March 2016
                : 18 May 2016
                Page count
                Pages: 11
                Funding
                Funded by: JSPS
                Funded by: KAKENHI
                Award ID: 24248045
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                feb412091
                August 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.4 mode:remove_FC converted:03.08.2016

                adipocyte,adipokine,extracellular matrix,proteomics,secreted proteins

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