Glucose-dependent insulin release from genetically engineered K cells

被引:214
作者
Cheung, AT
Dayanandan, B
Lewis, JT
Korbutt, GS
Rajotte, RV
Bryer-Ash, M
Boylan, MO
Wolfe, MM
Kieffer, TJ [1 ]
机构
[1] Univ Alberta, Dept Med, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Dept Physiol, Edmonton, AB T6G 2S2, Canada
[3] Univ Alberta, Dept Surg, Edmonton, AB T6G 2S2, Canada
[4] enGene Inc, Edmonton, AB T6G 2T5, Canada
[5] Univ Tennessee, Dept Med, Memphis, TN 38103 USA
[6] Boston Med Ctr, Gastroenterol Sect, Boston, MA 02118 USA
关键词
D O I
10.1126/science.290.5498.1959
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
Genetic engineering of non-beta cells to release insulin upon feeding could be a therapeutic modality for patients with diabetes. A tumor-derived K-cell line was induced to produce human insulin by providing the cells with the human insulin gene linked tb the 5'-regulatory region of the gene encoding glucose-dependent insulinotropic polypeptide (GIP). Mice expressing this transgene produced human insulin specifically in gut K cells. This insulin protected the mice from developing diabetes and maintained glucose tolerance after destruction of the native insulin-producing beta cells.
引用
收藏
页码:1959 / 1962
页数:4
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