Sonic hedgehog N-terminal level correlates with adiponectin level and insulin resistance in adolescents
Author:
Takaya Junji12, Tanabe Yuko2, Kaneko Kazunari2
Affiliation:
1. Department of Pediatrics , Kawachi General Hospital Higashi-Osaka , Osaka , Japan 2. Department of Pediatrics , Kansai Medical University Hirakata , Osaka , Japan
Abstract
Abstract
Objectives
Extracellular vesicles (EVs) are small vesicles released by nearly all types of cells. They deliver different types of substances, including proteins and nucleic acids, to nearby or distant cells and play a role in the mediation of cell-to-cell communication. The aim of this study was to explore the association between EVs and insulin resistance in adolescents with obesity or type 2 diabetes mellitus (DM2).
Methods
The subjects were eight adolescents with DM2 (DM2 group; four males and four females; age: 18.1 ± 2.3 years), 18 adolescents with simple obesity (obesity group; 12 males and six females; age: 12.2 ± 3.4 years), and 20 controls (control group; 10 males and 10 females; age: 13.0 ± 1.4 years). As markers of EVs, serum CD9/CD63 and sonic hedgehog N-terminal (Shh-N) levels were measured using enzyme-linked immunosorbent assay.
Results
The CD9/CD63 level in the control group was similar to that in the DM2 group, whereas the obesity group had a significantly higher CD9/CD63 level. In the entire study group, correlations were observed between serum Shh-N level and Homeostasis Model Assessment of insulin resistance (HOMA-IR) score (r=0.371, p=0.0143), Homeostasis Model Assessment-β cell function score (r=0.382, p=0.0115), serum insulin level (r=0.350, p=0.0171), and serum adiponectin level (r=0.367, p=0.0122). Multiple regression analysis revealed that serum Shh-N level was the most significant risk factor for HOMA-IR score and serum insulin level.
Conclusions
Shh is correlated with insulin resistance via its association with adiponectin in adolescents.
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Reference32 articles.
1. Kosaka, N, Iguchi, H, Yoshioka, Y, Takeshita, F, Matsuki, Y, Ochiya, T. Secretory mechanisms and intercellular transfer of microRNAs in living cells. J Biol Chem 2010;285:17442–52. https://doi.org/10.1074/jbc.m110.107821. 2. Valadi, H, Ekström, K, Bossios, A, Sjöstrand, M, Lee, JJ, Lötvall, JO. Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells. Nat Cell Biol 2007;9:654–9. https://doi.org/10.1038/ncb1596. 3. Simons, M, Raposo, G. Exosomes-vesicular carriers for intercellular communication. Curr Opin Cell Biol 2009;21:575–81. https://doi.org/10.1016/j.ceb.2009.03.007. 4. György, B, Szabó, TG, Pásztói, M, Pál, Z, Misják, P, Aradi, B, et al.. Membrane vesicles, current state-of-the-art: emerging role of extracellular vesicles. Cell Mol Life Sci 2011;68:2667–88. https://doi.org/10.1007/s00018-011-0689-3. 5. Müller, G, Schneider, M, Biemer-Daub, G, Wied, S. Upregulation of lipid synthesis in small rat adipocytes by microvesicle-associated CD73 from large adipocytes. Obesity 2011;19:1531–44. https://doi.org/10.1038/oby.2011.29.
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