Regenerating β cells of the pancreas - potential developments in diabetes treatment

被引:12
作者
Dong, Shengli [1 ]
Wu, Hongju [2 ]
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Dept Biochem & Mol Biol, New Orleans, LA USA
[2] Tulane Univ, Hlth Sci Ctr, Dept Med, New Orleans, LA 70118 USA
关键词
beta Cell regeneration; diabetes; stem cells; reprogramming; INSULIN-PRODUCING CELLS; IN-VITRO; STEM-CELLS; ALPHA-CELL; ISLET TRANSPLANTATION; PROGENITOR CELLS; TRANSCRIPTION FACTORS; FATE SPECIFICATION; ENDOCRINE PANCREAS; PRECURSOR CELLS;
D O I
10.1080/14712598.2018.1402885
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: The etiology of diabetes is mainly attributed to insulin deficiency due to the lack of beta cells (type 1), or to insulin resistance that eventually results in beta cell dysfunction (type 2). Therefore, an ultimate cure for diabetes requires the ability to replace the lost insulin-secreting beta cells. Strategies for regenerating beta cells are under extensive investigation. Areas covered: Herein, the authors first summarize the mechanisms underlying embryonic beta cell development and spontaneous adult beta cell regeneration, which forms the basis for developing beta cell regeneration strategies. Then the rationale and progress of each beta cell regeneration strategy is reviewed. Current beta cell regeneration strategies can be classified into two main categories: in vitro beta cell regeneration using pluripotent stem cells and in vivo reprogramming of non-beta cells into beta cells. Each has its own advantages and disadvantages. Expert opinion: Regenerating beta cells has shown its potential as a cure for the treatment of insulin-deficient diabetes. Much progress has been made, and beta cell regeneration therapy is getting closer to a clinical reality. Nevertheless, more hurdles need to be overcome before any of the strategies suggested can be fully translated from bench to bedside.
引用
收藏
页码:175 / 185
页数:11
相关论文
共 121 条
  • [1] Pancreatic β-cell regeneration: Facultative or dedicated progenitors?
    Afelik, Solomon
    Rovira, Meritxell
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2017, 445 (0C) : 85 - 94
  • [2] Ahlgren U, 1996, DEVELOPMENT, V122, P1409
  • [3] β-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the β-cell phenotype and maturity onset diabetes
    Ahlgren, U
    Jonsson, J
    Jonsson, L
    Simu, K
    Edlund, H
    [J]. GENES & DEVELOPMENT, 1998, 12 (12) : 1763 - 1768
  • [4] Single-Donor Islet Transplantation and Long-term Insulin Independence in Select Patients With Type 1 Diabetes Mellitus
    Al-Adra, David P.
    Gill, Richdeep S.
    Imes, Sharleen
    O'Gorman, Doug
    Kin, Tatsuya
    Axford, Sara J.
    Shi, Xinzhe
    Senior, Peter A.
    Shapiro, A. M. James
    [J]. TRANSPLANTATION, 2014, 98 (09) : 1007 - 1012
  • [5] Adult Duct-Lining Cells Can Reprogram into β-like Cells Able to Counter Repeated Cycles of Toxin-Induced Diabetes
    Al-Hasani, Keith
    Pfeifer, Anja
    Courtney, Monica
    Ben-Othman, Nouha
    Gjernes, Elisabet
    Vieira, Andhira
    Druelle, Noemie
    Avolio, Fabio
    Ravassard, Philippe
    Leuckx, Gunter
    Lacas-Gervais, Sandra
    Ambrosetti, Damien
    Benizri, Emmanuel
    Hecksher-Sorensen, Jacob
    Gounon, Pierre
    Ferrer, Jorge
    Gradwohl, Gerard
    Heimberg, Harry
    Mansouri, Ahmed
    Collombat, Patrick
    [J]. DEVELOPMENTAL CELL, 2013, 26 (01) : 86 - 100
  • [6] [Anonymous], 2017, National Diabetes Statistics Report - Estimates of Diabetes and Its Burden in the United States
  • [7] Reprogrammed Stomach Tissue as a Renewable Source of Functional β Cells for Blood Glucose Regulation
    Ariyachet, Chaiyaboot
    Tovaglieri, Alessio
    Xiang, Guanjue
    Lu, Jiaqi
    Shah, Manasvi S.
    Richmond, Camilla A.
    Verbeke, Catia
    Melton, Douglas A.
    Stanger, Ben Z.
    Mooney, David
    Shivdasani, Ramesh A.
    Mahony, Shaun
    Xia, Qing
    Breault, David T.
    Zhou, Qiao
    [J]. CELL STEM CELL, 2016, 18 (03) : 410 - 421
  • [8] RETRACTED: Transient cytokine treatment induces acinar cell reprogramming and regenerates functional beta cell mass in diabetic mice (Retracted Article)
    Baeyens, Luc
    Lemper, Marie
    Leuckx, Gunter
    De Groef, Sofie
    Bonfanti, Paola
    Stange, Geert
    Shemer, Ruth
    Nord, Christoffer
    Scheel, David W.
    Pan, Fong C.
    Ahlgren, Ulf
    Gu, Guoqiang
    Stoffers, Doris A.
    Dor, Yuval
    Ferrer, Jorge
    Gradwohl, Gerard
    Wright, Christopher V. E.
    Van de Casteele, Mark
    German, Michael S.
    Bouwens, Luc
    Heimberg, Harry
    [J]. NATURE BIOTECHNOLOGY, 2014, 32 (01) : 76 - +
  • [9] The functional and molecular characterisation of human embryonic stem cell-derived insulin-positive cells compared with adult pancreatic beta cells
    Basford, C. L.
    Prentice, K. J.
    Hardy, A. B.
    Sarangi, F.
    Micallef, S. J.
    Li, X.
    Guo, Q.
    Elefanty, A. G.
    Stanley, E. G.
    Keller, G.
    Allister, E. M.
    Nostro, M. C.
    Wheeler, M. B.
    [J]. DIABETOLOGIA, 2012, 55 (02) : 358 - 371
  • [10] Sustained proliferation of PDX-1+ cells derived from human islets
    Beattie, GM
    Itkin-Ansari, P
    Cirulli, V
    Leibowitz, G
    Lopez, AD
    Bossie, S
    Mally, MI
    Levine, F
    Hayek, A
    [J]. DIABETES, 1999, 48 (05) : 1013 - 1019