Department of Biological Sciences, The George Washington University, Washington, District of Columbia, United States of America.
PLoS One. 2013 Sep 3;8(9):e73080. doi: 10.1371/journal.pone.0073080. eCollection 2013.
Toxic human amylin oligomers and aggregates are implicated in the pathogenesis of type 2 diabetes mellitus (TTDM). Although recent studies have shown that pancreatic cells can recycle amylin monomers and toxic oligomers, the exact uptake mechanism and trafficking routes of these molecular forms and their significance for amylin toxicity are yet to be determined. Using pancreatic rat insulinoma (RIN-m5F) beta (β)-cells and human islets as model systems we show that monomers and oligomers cross the plasma membrane (PM) through both endocytotic and non-endocytotic (translocation) mechanisms, the predominance of which is dependent on amylin concentrations and incubation times. At low (≤ 100 nM) concentrations, internalization of amylin monomers in pancreatic cells is completely blocked by the selective amylin-receptor (AM-R) antagonist, AC-187, indicating an AM-R dependent mechanism. In contrast at cytotoxic (µM) concentrations monomers initially (1 hour) enter pancreatic cells by two distinct mechanisms: translocation and macropinocytosis. However, during the late stage (24 hours) monomers internalize by a clathrin-dependent but AM-R and macropinocytotic independent pathway. Like monomers a small fraction of the oligomers initially enter cells by a non-endocytotic mechanism. In contrast a majority of the oligomers at both early (1 hour) and late times (24 hours) traffic with a fluid-phase marker, dextran, to the same endocytotic compartments, the uptake of which is blocked by potent macropinocytotic inhibitors. This led to a significant increase in extra-cellular PM accumulation, in turn potentiating amylin toxicity in pancreatic cells. Our studies suggest that macropinocytosis is a major but not the only clearance mechanism for both amylin's molecular forms, thereby serving a cyto-protective role in these cells.
有毒的人类胰岛淀粉样多肽寡聚物和聚集体与 2 型糖尿病(T2DM)的发病机制有关。尽管最近的研究表明,胰腺细胞可以回收胰岛淀粉样多肽单体和有毒的寡聚物,但是这些分子形式的摄取机制和运输途径及其对胰岛淀粉样多肽毒性的意义仍有待确定。我们使用胰腺大鼠胰岛素瘤(RIN-m5F)β(β)-细胞和人胰岛作为模型系统,表明单体和寡聚体能通过内吞作用和非内吞作用(易位)机制穿过质膜(PM),其优势取决于胰岛淀粉样多肽的浓度和孵育时间。在低浓度(≤100 nM)下,胰岛淀粉样多肽单体在胰腺细胞中的内化完全被选择性胰岛淀粉样多肽受体(AM-R)拮抗剂 AC-187 阻断,表明这是一种 AM-R 依赖性机制。相比之下,在细胞毒性(µM)浓度下,单体最初(1 小时)通过两种不同的机制进入胰腺细胞:易位和巨胞饮作用。然而,在晚期(24 小时),单体通过网格蛋白依赖性但 AM-R 和巨胞饮作用独立的途径内化。与单体一样,一小部分寡聚体能通过非内吞作用机制最初进入细胞。相比之下,大部分寡聚体在早期(1 小时)和晚期(24 小时)与一种流体相标记物葡聚糖一起运输到相同的内吞小泡中,其摄取被有效的巨胞饮抑制剂阻断。这导致细胞外质膜(PM)积累的显著增加,从而增强了胰岛淀粉样多肽在胰腺细胞中的毒性。我们的研究表明,巨胞饮作用是两种胰岛淀粉样多肽分子形式的主要但不是唯一的清除机制,因此在这些细胞中发挥细胞保护作用。