Precision Health Program, Department of Radiology, College of Human Medicine, Michigan State University, East Lansing, Michigan, 48823, USA.
Department of Anatomy, Histology and Embryology, School of Basic Medical Science, Fudan University, Shanghai, 200032, China.
Sci Rep. 2020 Mar 24;10(1):5302. doi: 10.1038/s41598-020-62269-4.
Aberrant expression of miRNAs in pancreatic islets is closely related to the development of type 1 diabetes (T1D). The aim of this study was to identify key miRNAs dysregulated in pancreatic islets during T1D progression and to develop a theranostic approach to modify their expression using an MRI-based nanodrug consisting of iron oxide nanoparticles conjugated to miRNA-targeting oligonucleotides in a mouse model of T1D. Isolated pancreatic islets were derived from NOD mice of three distinct age groups (3, 8 and 18-week-old). Total RNA collected from cultured islets was purified and global miRNA profiling was performed with 3D-Gene global miRNA microarray mouse chips encompassing all mouse miRNAs available on the Sanger miRBase V16. Of the miRNAs that were found to be differentially expressed across three age groups, we identified one candidate (miR-216a) implicated in beta cell proliferation for subsequent validation by RT-PCR. Alterations in miR-216a expression within pancreatic beta cells were also examined using in situ hybridization on the frozen pancreatic sections. For in vitro studies, miR-216a mimics/inhibitors were conjugated to iron oxide nanoparticles and incubated with beta cell line, βTC-6. Cell proliferation marker Ki67 was evaluated. Expression of the phosphatase and tensin homolog (PTEN), which is one of the direct targets of miR-216a, was analyzed using western blot. For in vivo study, the miR-216a mimics/inhibitors conjugated to the nanoparticles were injected into 12-week-old female diabetic Balb/c mice via pancreatic duct. The delivery of the nanodrug was monitored by in vivo MRI. Blood glucose of the treated mice was monitored post injection. Ex vivo histological analysis of the pancreatic sections included staining for insulin, PTEN and Ki67. miRNA microarray demonstrated that the expression of miR-216a in the islets from NOD mice significantly changed during T1D progression. In vitro studies showed that treatment with a miR-216a inhibitor nanodrug suppressed proliferation of beta cells and increased the expression of PTEN, a miR-216a target. In contrast, introduction of a mimic nanodrug decreased PTEN expression and increased beta cell proliferation. Animals treated in vivo with a mimic nanodrug had higher insulin-producing functionality compared to controls. These observations were in line with downregulation of PTEN and increase in beta cell proliferation in that group. Our studies demonstrated that miR-216a could serve as a potential therapeutic target for the treatment of diabetes. miR-216a-targeting theranostic nanodrugs served as exploratory tools to define functionality of this miRNA in conjunction with in vivo MR imaging.
胰岛中 miRNAs 的异常表达与 1 型糖尿病(T1D)的发展密切相关。本研究旨在鉴定 T1D 进展过程中胰岛中失调的关键 miRNAs,并开发一种治疗方法,通过一种 MRI 为基础的纳米药物来修饰它们的表达,该纳米药物由氧化铁纳米粒子与 miRNA 靶向寡核苷酸结合而成,应用于 T1D 小鼠模型。从三组不同年龄(3、8 和 18 周龄)的 NOD 小鼠中分离出胰岛。从培养的胰岛中提取总 RNA,使用涵盖 Sanger miRBase V16 上所有小鼠 miRNA 的 3D-Gene 全局 miRNA 微阵列小鼠芯片进行全局 miRNA 谱分析。在三组中发现差异表达的 miRNAs 中,我们鉴定出一个候选 miRNA(miR-216a),该 miRNA 参与β细胞增殖,随后通过 RT-PCR 进行验证。还使用冷冻胰腺切片上的原位杂交技术检查了 miR-216a 在胰岛β细胞中的表达变化。在体外研究中,将 miR-216a 模拟物/抑制剂与氧化铁纳米粒子结合,并与βTC-6 细胞系共孵育。评估细胞增殖标志物 Ki67。使用 Western blot 分析 miR-216a 的直接靶标之一磷酸酶和张力蛋白同源物(PTEN)的表达。在体内研究中,将与纳米颗粒结合的 miR-216a 模拟物/抑制剂通过胰腺管注入 12 周龄雌性糖尿病 Balb/c 小鼠体内。通过体内 MRI 监测纳米药物的递送。注射后监测治疗小鼠的血糖。对胰腺切片进行离体组织学分析,包括胰岛素、PTEN 和 Ki67 的染色。miRNA 微阵列显示,在 T1D 进展过程中,NOD 小鼠胰岛中的 miR-216a 表达显著改变。体外研究表明,用 miR-216a 抑制剂纳米药物治疗可抑制β细胞增殖并增加 miR-216a 靶标 PTEN 的表达。相反,引入模拟物纳米药物会降低 PTEN 的表达并增加β细胞增殖。与对照组相比,体内用模拟物纳米药物治疗的动物具有更高的胰岛素产生功能。这些观察结果与该组中 PTEN 的下调和β细胞增殖的增加一致。我们的研究表明,miR-216a 可作为治疗糖尿病的潜在治疗靶点。miR-216a 靶向治疗性纳米药物作为探索性工具,结合体内 MR 成像来定义该 miRNA 的功能。