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. 2013 May 20;62(6):1904–1912. doi: 10.2337/db12-0769

FIG. 4.

FIG. 4.

Human islet PTGER3 and PGE2 synthetic enzyme expression is positively associated with donor obesity and T2D status, correlating with increased PGE2 production from confirmed T2D human islets. A: Cultured islets from human cadaveric donors were grouped as nonobese (BMI <30 kg/m2, n = 13) or obese (BMI ≥30 kg/m2, n = 12) (left panel) or confirmed T2D (n = 3) vs. nondiabetic (ND) (n = 3) (right panel). Confirmed T2D donors were matched as closely as possible with nondiabetic donors for sex, race, age, and BMI (all female; both groups with Caucasian and African American donors; mean ± SD age 46.3 ± 2.1 years (nondiabetic) vs. 54.3 ± 5.7 years (T2D; P = 0.32) and BMI 28.1 ± 7.3 kg/m2 (nondiabetic) vs. 25.4 ± 2.1 kg/m2 (T2D; P = 0.57). Islet cDNA was subjected to qRT PCR analysis for PTGER3, PTGS2, PTGES, and PTGES2 expression. Expression data were compared by unpaired t test (#P = 0.11; *P < 0.05). B: PGE2 production was measured from islets obtained from nondiabetic or confirmed T2D human donors. Islets were cultured for 24 h (hr), and the PGE2 secreted into the medium was normalized to the total number of islets. Data were compared by unpaired t test (n = 3). *P < 0.05.