Diabetes treatment by conversion of gut epithelial cells to insulin-producing cells

被引:0
|
作者
Accili, Domenico [1 ,2 ]
Talchai, Shivatra C. [3 ]
Bouchi, Ryotaro [4 ]
Lee, April Yun-Kyoung [5 ]
Du, Wen [6 ]
Kitamoto, Takumi [7 ]
McKimpson, Wendy M. [1 ,2 ]
Belvedere, Sandro [8 ,9 ]
Lin, Hua, V [10 ]
机构
[1] Columbia Univ, Vagelos Coll Phys & Surg, Dept Med, New York, NY 10027 USA
[2] Columbia Univ, Vagelos Coll Phys & Surg, Naomi Berrie Diabet Ctr, New York, NY 10027 USA
[3] Medeze Grp Pte Ltd, Singapore, Singapore
[4] Natl Ctr Global Hlth & Med, Diabet Res Ctr, Diabet & Metab Informat Ctr, Res Inst, Tokyo, Japan
[5] Regeneron Pharmaceut, Tarrytown, NY USA
[6] Guangzhou Med Univ, Sch Biomed Engn, Guangzhou, Peoples R China
[7] Chiba Univ Hosp, Dept Diabet Metab & Endocrinol, Chiba, Japan
[8] ARMGO Pharm Inc, Ardsley, NY USA
[9] Avicenna Biosci Inc, Durham, NC USA
[10] Render Therapeut, Lincoln, MA USA
基金
美国国家卫生研究院;
关键词
autoimmunity; diabetes; intestine; BETA-CELLS; GLUCOSE; ENDOCRINE;
D O I
10.1111/jdi.14175
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin-deficient (type 1) diabetes is treated by providing insulin to maintain euglycemia. The current standard of care is a quasi-closed loop integrating automated insulin delivery with a continuous glucose monitoring sensor. Cell replacement technologies are advancing as an alternative treatment and have been tested as surrogates to cadaveric islets in transplants. In addition, immunomodulatory treatments to delay the onset of type 1 diabetes in high-risk (stage 2) individuals have gained regulatory approval. We have pioneered a cell conversion approach to restore insulin production through pharmacological conversion of intestinal epithelial cells into insulin-producing cells. We have advanced this approach along a translational trajectory through the discovery of small molecule forkhead box protein O1 inhibitors. When administered to different rodent models of insulin-deficient diabetes, these inhibitors have resulted in robust glucose-lowering responses and generation of insulin-producing cells in the gut epithelium. We review past work and delineate a path to human clinical trials. Converting gut cells into insulin-producing cells has emerged as an attractive therapeutic option to treat diabetes. Here, we summarize this field and review its clinical potential. image
引用
收藏
页码:797 / 804
页数:8
相关论文
共 50 条
  • [31] In Vivo Regeneration of Insulin-Producing β-Cells
    Jun, Hee-Sook
    ISLETS OF LANGERHANS, 2010, 654 : 627 - 640
  • [32] Transplantation of Macroencapsulated Insulin-Producing Cells
    Hwa, Albert J.
    Weir, Gordon C.
    CURRENT DIABETES REPORTS, 2018, 18 (08)
  • [33] Author Correction: Insulin-producing organoids engineered from islet and amniotic epithelial cells to treat diabetes
    Fanny Lebreton
    Vanessa Lavallard
    Kevin Bellofatto
    Romain Bonnet
    Charles H. Wassmer
    Lisa Perez
    Vakhtang Kalandadze
    Antonia Follenzi
    Michel Boulvain
    Julie Kerr-Conte
    David J. Goodman
    Domenico Bosco
    Thierry Berney
    Ekaterine Berishvili
    Nature Communications, 11
  • [34] New sources for insulin-producing cells
    Al-Turaifi, Hussain R.
    SAUDI MEDICAL JOURNAL, 2013, 34 (03) : 232 - 239
  • [35] Cell therapy of diabetes with insulin-producing cells derived from adult stem cells
    Seissler, J
    Schmiegelt, D
    Ruetter, R
    Wohlrab, U
    DIABETOLOGIA, 2005, 48 : A148 - A148
  • [37] Accumulation of cadmium in insulin-producing β cells
    El Muayed, Malek
    Raja, Meera R.
    Zhang, Xiaomin
    MacRenaris, Keith W.
    Bhatt, Surabhi
    Chen, Xiaojuan
    Urbanek, Margrit
    O'Halloran, Thomas V.
    Lowe, William L., Jr.
    ISLETS, 2012, 4 (06) : 405 - 416
  • [38] Location matters for insulin-producing cells
    Spagnoli, Francesca M.
    NATURE, 2018, 564 (7734) : 50 - 51
  • [39] The role of mimitin in insulin-producing cells
    Hanzelka, K.
    Gurgul-Convey, E.
    Jura, J.
    Lenzen, S.
    DIABETOLOGIA, 2009, 52 : S154 - S154
  • [40] Stem Cell-Derived Insulin-Producing β Cells to Treat Diabetes
    Harb G.
    Poh Y.-C.
    Pagliuca F.
    Current Transplantation Reports, 2017, 4 (3) : 202 - 210