However, there is still so much diversity between the two groups

However, there is still so much diversity between the two groups of cells. These differences might provide a future research direction to figure out how to optimize differentiation into IPCs. In our study, we only tested the difference between one kind of IPC and normal human pancreatic beta cells. Therefore, our results are not enough

to elucidate the relationship between cellular ultrastructure and function. In order to explore the relationship between cellular structure and cell function, we need to study the links between cell function and more cell membrane proteins, as well as analyze various types of endocrine cells by looking for the common cellular surface ultrastructure. Acknowledgments This work was funded by the Guangdong Provincial Science and Technology Project of China (2010B031600105, 2011B031800066),

granted from the Guangdong Provincial Medical Scientific Research Foundation A-1210477 (B2011161), and supported by the National Natural Science Foundation of China (973 program projects, 2010CB833603) and the Fundamental Research Funds for the Central Universities. References 1. Venstrom JM, McBride MA, Rother KI, Hirshberg B, Orchard TJ, Harlan DM: Survival after pancreas transplantation in patients with diabetes and preserved kidney function. JAMA 2003, 290:2817–2823.CrossRef 2. Campbell PM, Senior PA, Salam A, LaBranche K, Bigam DL, Kneteman NM, Imes S, Halpin A, Ryan EA, Shapiro AMJ: High risk of sensitization after failed islet transplantation. Am J Transplant 2007, 7:2311–2317.CrossRef 3. Korsgren O, Nilsson B, Berne C, Felldin M, Foss A, Kallen R, Lundgren T, Salmela K, Tibell find more A, Tufveson G: Current status of clinical islet transplantation. Transplantation 2005, 79:1289–1293.CrossRef 4. Ryan EA, Lakey JR, Rajotte RV, Korbutt GS, Kim T, Imes S, Rabinovitch A, Elliott JF, Bigam D, Kneteman NM, Warnock GL, Larsen I, Shapiro AJ: Clinical outcomes and insulin secretion after islet transplantation with the Edmonton protocol. Diabetes 2001, 50:710–719.CrossRef

5. Porat S, Dor Y: New sources of pancreatic beta-cells. Curr Diab Rep 2007, 7:304–308.CrossRef 6. Rolletschek A, Kania G, Wobus AM: Generation of pancreatic insulin-producing cells from embryonic stem cells—“proof of Thalidomide principle”, but buy CBL0137 questions still unanswered. Diabetologia 2006, 49:2541–2545.CrossRef 7. Fujikawa T, Oh SH, Pi L, Hatch HM, Shupe T, Petersen BE: Teratoma formation leads to failure of treatment for type I diabetes using embryonic stem cell derived insulin-producing cells. Am J Pathol 2005, 166:1781–1791.CrossRef 8. Kroon E, Martinson LA, Kadoya K, Bang AG, Kelly OG, Eliazer S, Young H, Richardson M, Smart NG, Cunningham J, Agulnick AD, D’Amour KA, Carpenter MK, Baetge EE: Pancreatic endoderm derived from human embryonic stem cells generates glucose-responsive insulin-secreting cells in vivo. Nat Biotechnol 2008, 26:443–452.CrossRef 9. Fellous TG, Guppy NJ, Brittan M, Alison MR: Cellular pathways to β-cell replacement.

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