Synthetic beta cells for fusion-mediated dynamic insulin secretion

被引:0
|
作者
Chen, Zhaowei [1 ,2 ,3 ,4 ]
Wang, Jinqiang [1 ,2 ,3 ,4 ]
Sun, Wujin [1 ,2 ,3 ,4 ]
Archibong, Edikan [1 ,2 ]
Kahkoska, Anna R.
Zhang, Xudong [1 ,2 ,3 ,4 ]
Lu, Yue [1 ,2 ,3 ,4 ]
Ligler, Frances S. [1 ,2 ]
Buse, John B. [5 ]
Gu, Zhen [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ North Carolina Chapel Hill, Joint Dept Biomed Engn, Raleigh, NC 27695 USA
[2] North Carolina State Univ, Raleigh, NC 27695 USA
[3] Univ North Carolina Chapel Hill, Div Pharmacoengn & Mol Pharmaceut, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Ctr Nanotechnol Drug Delivery, Eshelman Sch Pharm, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Sch Med, Dept Med, Chapel Hill, NC USA
基金
美国国家科学基金会;
关键词
GLUCOSE-RESPONSIVE INSULIN; ARTIFICIAL CELLS; VESICLES; COMPLICATIONS; TRANSPORT; DETERMINANTS; COMPARTMENTS; PEGYLATION; PROTEIN; MODEL;
D O I
10.1038/NCHEMBIO.2511
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Generating artificial pancreatic beta cells by using synthetic materials to mimic glucose-responsive insulin secretion in a robust manner holds promise for improving clinical outcomes in people with diabetes. Here, we describe the construction of artificial beta cells (A beta Cs) with a multicompartmental 'vesicles-in-vesicle' superstructure equipped with a glucose-metabolism system and membrane-fusion machinery. Through a sequential cascade of glucose uptake, enzymatic oxidation and proton efflux, the A beta Cs can effectively distinguish between high and normal glucose levels. Under hyperglycemic conditions, high glucose uptake and oxidation generate a low pH (<5.6), which then induces steric deshielding of peptides tethered to the insulin-loaded inner small liposomal vesicles. The peptides on the small vesicles then form coiled coils with the complementary peptides anchored on the inner surfaces of large vesicles, thus bringing the membranes of the inner and outer vesicles together and triggering their fusion and insulin 'exocytosis'.
引用
收藏
页码:86 / +
页数:12
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