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©2014 Baishideng Publishing Group Inc.
World J Diabetes. Aug 15, 2014; 5(4): 511-526
Published online Aug 15, 2014. doi: 10.4239/wjd.v5.i4.511
Published online Aug 15, 2014. doi: 10.4239/wjd.v5.i4.511
Figure 1 A schematic representation of SH2B1 isoforms.
DD: Dimerization domain; PH: PH domain; SH2: SH2 domain; Y: Tyrosine; Numbers: Amino acid numbers.
Figure 2 A model of Src homology 2B1 regulation of leptin signaling.
The Src homology 2B1 (SH2B1) homodimers bind to JAK2, IRS1, and/or IRS2. SH2B1-JAK2 interaction increases JAK2 kinase activity, thus globally enhancing leptin signaling. JAK2 phosphorylates STAT3 which subsequently homodimerizes, translocates into the nucleus, and activates its target genes. SH2B1-IRS1/2 interaction allows JAK2 to phosphorylate IRS proteins which subsequently activate the PI 3-kinase pathway. Both the STAT3 and the PI 3-kinase pathways are required for leptin to control energy balance and body weight. JAK2: Janus kinase 2; IRS1: Insulin receptor substrate-1; STAT3: Signal transducer and activator of transcription 3.
Figure 3 A schematic representation of SH2B2 isoforms.
DD: Dimerization domain; PH: PH domain; SH2: SH2 domain; Y: Tyrosine.
- Citation: Rui L. SH2B1 regulation of energy balance, body weight, and glucose metabolism. World J Diabetes 2014; 5(4): 511-526
- URL: https://www.wjgnet.com/1948-9358/full/v5/i4/511.htm
- DOI: https://dx.doi.org/10.4239/wjd.v5.i4.511