GLUT4-overexpressing engineered muscle constructs as a therapeutic platform to normalize glycemia in diabetic mice

被引:22
作者
Beckerman, Margarita [1 ,2 ]
Harel, Chava [2 ,3 ]
Michael, Inbal [1 ]
Klip, Amira [4 ]
Bilan, Philip J. [4 ]
Gallagher, Emily J. [5 ]
LeRoith, Derek [5 ]
Lewis, Eli C. [6 ]
Karnieli, Eddy [2 ,3 ]
Levenberg, Shulamit [1 ,2 ]
机构
[1] Technion Israel Inst Technol, Fac Biomed Engn, Haifa, Israel
[2] Technion Israel Inst Technol, Rina & Avner Schneur Ctr Diabet Res, Haifa, Israel
[3] Technion Israel Inst Technol, Rappaport Fac Med, Haifa, Israel
[4] Hosp Sick Children, Program Cell Biol, Toronto, ON, Canada
[5] Ichan Sch Med Mt Sinai, Samuel Bronfman Dept Med, Div Endocrinol Diabet & Bone Dis, New York, NY 10029 USA
[6] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Clin Biochem & Pharmacol, Beer Sheva, Israel
关键词
SKELETAL-MUSCLE; INSULIN-RESISTANCE; GLUT4; TRANSLOCATION; GLUCOSE; OVEREXPRESSION; EXPRESSION; OBESITY; INACTIVATION; SENSITIVITY; EXERCISE;
D O I
10.1126/sciadv.abg3947
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Skeletal muscle insulin resistance is a main defect in type 2 diabetes (T2D), which is associated with impaired function and content of glucose transporter type 4 (GLUT4). GLUT4 overexpression in skeletal muscle tissue can improve glucose homeostasis. Therefore, we created an engineered muscle construct (EMC) composed of GLUT4-overexpressing (OEG4) cells. The ability of the engineered implants to reduce fasting glucose levels was tested in diet-induced obesity mice. Decrease and stabilization of basal glucose levels were apparent up to 4 months after implantation. Analysis of the retrieved constructs showed elevated expression of myokines and proteins related to metabolic processes. In addition, we validated the efficiency of OEG4-EMCs in insulin-resistant mice. Following high glucose load administration, mice showed improved glucose tolerance. Our data indicate that OEG4-EMC implant is an efficient mode for restoring insulin sensitivity and improving glucose homeostasis in diabetic mice. Such procedure is a potential innovative modality for T2D therapy.
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页数:13
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