Regeneration of insulin-producing beta-cells as well as islet transplantation is the most promising long-term solutions for Type 1 diabetes (T1D) treatment. A major obstacle to the success of this approach is the shortage of organ donors and the necessity for life-long immunosupression after allograft transplantation. Two recent advances, the success in reprogramming somatic cells into pluripotent ES cell-like IPS (induced pluripotent stem) cells and the success in differentiation of human ES cells into functional islet-like clusters (ILCs), have opened the possibility of generating patient-specific insulin-secreting ILCs through the reprogramming of somatic cells into iPS cells followed by guided differentiation. Indeed, in a proof-of-concept study, we have recently demonstrated that insulin-secreting cells can be generated from human skin fibroblasts using this approach. Despite this encouraging result, several obstacles have to be overcome before the value of this technique can be realized clinically. The major obstacles include: 1) safety concerns over the use of iPS cells that harbor viral vectors;2) low efficiency of current protocols in generating functional beta-cells;3) autoimmune destruction of the transplanted beta-cells. Given that the large iPS cell community is attacking the first problem and many immunology labs are trying to solve the third problem, the current proposal plans to use epigenetic, chemical, and ECM approaches to attack the second issue.
The Specific Aims are: 1) Characterization of epigenetic features of fetal and mature human beta-cells; 2) Characterization of epigenetic features of definitive endoderm, pancreatic progenitors, and endocrine progenitors; 3) Identification of chemical molecules that promote beta-cell differentiation; 4) Characterization of the effect of extracellular matrix and other environmental factors on beta-cell differentiation;
Beta cell regeneration is a promising longterm solution for diabetes treatment. In this study we propse to use a comprehensive approaches that include epigenetic, chemical, ECM and 3D culture to improve the efficiency of generating functional beta-cells from hES and hiPS cells for the development of a cell replacement therapy for T1D.
|Wu, Hao; Zhang, Yi (2015) Charting oxidized methylcytosines at base resolution. Nat Struct Mol Biol 22:656-61|
|Jiang, Wei; Liu, Yuting; Liu, Rui et al. (2015) The lncRNA DEANR1 facilitates human endoderm differentiation by activating FOXA2 expression. Cell Rep 11:137-48|
|Inoue, Azusa; Shen, Li; Matoba, Shogo et al. (2015) Haploinsufficiency, but not defective paternal 5mC oxidation, accounts for the developmental defects of maternal Tet3 knockouts. Cell Rep 10:463-70|
|Wu, Hao; Wu, Xiaoji; Shen, Li et al. (2014) Single-base resolution analysis of active DNA demethylation using methylase-assisted bisulfite sequencing. Nat Biotechnol 32:1231-40|
|Tuesta, Luis M; Zhang, Yi (2014) Mechanisms of epigenetic memory and addiction. EMBO J 33:1091-103|
|Matoba, Shogo; Liu, Yuting; Lu, Falong et al. (2014) Embryonic development following somatic cell nuclear transfer impeded by persisting histone methylation. Cell 159:884-95|
|Shen, Li; Song, Chun-Xiao; He, Chuan et al. (2014) Mechanism and function of oxidative reversal of DNA and RNA methylation. Annu Rev Biochem 83:585-614|
|Shen, Li; Inoue, Azusa; He, Jin et al. (2014) Tet3 and DNA replication mediate demethylation of both the maternal and paternal genomes in mouse zygotes. Cell Stem Cell 15:459-70|
|Lu, Falong; Liu, Yuting; Jiang, Lan et al. (2014) Role of Tet proteins in enhancer activity and telomere elongation. Genes Dev 28:2103-19|
|Wu, Hao; Zhang, Yi (2014) Reversing DNA methylation: mechanisms, genomics, and biological functions. Cell 156:45-68|
Showing the most recent 10 out of 32 publications