Kurian Sunil M, Ferreri Kevin, Wang Chia-Hao, Todorov Ivan, Al-Abdullah Ismail H, Rawson Jeffrey, Mullen Yoko, Salomon Daniel R, Kandeel Fouad
Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California, United States of America.
Department of Translational Research and Cellular Therapeutics, Diabetes, and Metabolism Research Institute, City of Hope National Medical Center, Duarte, California, United States of America.
PLoS One. 2017 Oct 2;12(10):e0185331. doi: 10.1371/journal.pone.0185331. eCollection 2017.
There is growing evidence that transplantation of cadaveric human islets is an effective therapy for type 1 diabetes. However, gauging the suitability of islet samples for clinical use remains a challenge. We hypothesized that islet quality is reflected in the expression of specific genes. Therefore, gene expression in 59 human islet preparations was analyzed and correlated with diabetes reversal after transplantation in diabetic mice. Analysis yielded 262 differentially expressed probesets, which together predict islet quality with 83% accuracy. Pathway analysis revealed that failing islet preparations activated inflammatory pathways, while functional islets showed increased regeneration pathway gene expression. Gene expression associated with apoptosis and oxygen consumption showed little overlap with each other or with the 262 probeset classifier, indicating that the three tests are measuring different aspects of islet cell biology. A subset of 36 probesets surpassed the predictive accuracy of the entire set for reversal of diabetes, and was further reduced by logistic regression to sets of 14 and 5 without losing accuracy. These genes were further validated with an independent cohort of 16 samples. We believe this limited number of gene classifiers in combination with other tests may provide complementary verification of islet quality prior to their clinical use.
越来越多的证据表明,移植尸体人胰岛是治疗1型糖尿病的有效方法。然而,评估胰岛样本用于临床的适用性仍然是一项挑战。我们假设胰岛质量反映在特定基因的表达中。因此,分析了59份人胰岛制剂中的基因表达,并将其与糖尿病小鼠移植后的糖尿病逆转情况相关联。分析产生了262个差异表达的探针集,它们共同预测胰岛质量的准确率为83%。通路分析显示,失败的胰岛制剂激活了炎症通路,而功能正常的胰岛显示再生通路基因表达增加。与细胞凋亡和氧消耗相关的基因表达彼此之间以及与262个探针集分类器几乎没有重叠,表明这三项测试测量的是胰岛细胞生物学的不同方面。36个探针集的一个子集在糖尿病逆转方面超过了整个集合的预测准确率,并通过逻辑回归进一步减少到14个和5个集合而不损失准确率。这些基因在一个由16个样本组成的独立队列中得到了进一步验证。我们相信,这有限数量的基因分类器与其他测试相结合,可能在胰岛临床使用前提供胰岛质量的补充验证。