Department of Internal Medicine, Jeju National University School of Medicine, Jeju, Republic of Korea 690-756.
J Clin Endocrinol Metab. 2013 Jun;98(6):2553-61. doi: 10.1210/jc.2012-4288. Epub 2013 Mar 28.
Dipeptidyl peptidase 4 (CD26/DPP4) is expressed on blood T cells and also circulates in a soluble form (sCD26/DPP4).
We aimed to evaluate blood T cell and circulating CD26/DPP4 and its association with metabolic parameters in patients with type 2 diabetes mellitus (T2DM).
We measured CD26/DPP4 expression (percentage of CD26(+) cells using flow cytometry) on CD4(+) and CD8(+) T cells, serum CD26/DPP4 level and activity, and various metabolic parameters in T2DM patients not on DPP4 inhibitor therapy (n = 148). Nondiabetic subjects (n = 50) were included as a control group.
Compared with the healthy controls, CD26/DPP4 expression on CD4(+) T cells and CD8(+) T cells was higher in T2DM patients. Serum CD26/DPP4 levels and enzymatic activities were also higher in patients with T2DM than in the control group only when metformin and/or thiazolidinedione-treated T2DM patients were excluded; metformin and/or thiazolidinedione-treated T2DM patients had lower values compared with other T2DM patients. Various parameters in T2DM patients were related to CD26/DPP4 expression on the T cells (hemoglobin A1c), serum sCD26/DPP4 (hemoglobin A1c and insulin resistance assessed by updated homeostasis model assessment), and serum CD26/DPP4 activity (insulin resistance assessed by updated homeostasis model assessment, γ-glutamyl transferase, and alanine aminotransferase) by multivariate analyses. After active glucose control for 12 weeks in drug-naive T2DM patients (n = 50), CD26/DPP4 expression on blood T cells was significantly decreased.
Our results suggest that the CD26/DPP4 level on blood T cells was associated with glucose control status in patients with T2DM.
二肽基肽酶 4(CD26/DPP4)在血液 T 细胞上表达,也以可溶性形式(sCD26/DPP4)循环。
我们旨在评估 2 型糖尿病(T2DM)患者的血液 T 细胞和循环 CD26/DPP4及其与代谢参数的关系。
我们使用流式细胞术测量了未接受 DPP4 抑制剂治疗的 T2DM 患者(n=148)的 CD4+和 CD8+T 细胞上的 CD26/DPP4 表达(CD26+细胞的百分比)、血清 CD26/DPP4 水平和活性以及各种代谢参数。还纳入了非糖尿病受试者(n=50)作为对照组。
与健康对照组相比,T2DM 患者的 CD4+和 CD8+T 细胞上的 CD26/DPP4 表达更高。只有排除接受二甲双胍和/或噻唑烷二酮治疗的 T2DM 患者时,T2DM 患者的血清 CD26/DPP4 水平和酶活性才高于对照组;与其他 T2DM 患者相比,二甲双胍和/或噻唑烷二酮治疗的 T2DM 患者的数值更低。T2DM 患者的各种参数与 T 细胞上的 CD26/DPP4 表达(糖化血红蛋白 A1c)、血清 sCD26/DPP4(糖化血红蛋白 A1c 和通过更新的稳态模型评估的胰岛素抵抗)和血清 CD26/DPP4 活性(通过更新的稳态模型评估的胰岛素抵抗、γ-谷氨酰转移酶和丙氨酸氨基转移酶)相关通过多元分析。在未经药物治疗的 T2DM 患者(n=50)进行 12 周积极血糖控制后,血液 T 细胞上的 CD26/DPP4 表达显著降低。
我们的结果表明,T2DM 患者血液 T 细胞上的 CD26/DPP4 水平与血糖控制状态有关。