Stage-specific signaling through TGFβ family members and WNT regulates patterning and pancreatic specification of human pluripotent stem cells

被引:289
作者
Nostro, M. Cristina [1 ]
Sarangi, Farida [1 ]
Ogawa, Shinichiro [1 ]
Holtzinger, Audrey [1 ]
Corneo, Barbara [2 ]
Li, Xueling [3 ]
Micallef, Suzanne J. [3 ]
Park, In-Hyun [4 ]
Basford, Christina [5 ]
Wheeler, Michael B. [5 ]
Daley, George Q. [6 ,7 ]
Elefanty, Andrew G. [3 ]
Stanley, Edouard G. [3 ]
Keller, Gordon [1 ]
机构
[1] Univ Hlth Network, McEwen Ctr Regenerat Med, Toronto, ON M5G 1L7, Canada
[2] New York Neural Stem Cell Inst, Rensselaer, NY 12144 USA
[3] Monash Univ, Monash Immunol & Stem Cell Labs, Clayton, Vic 3800, Australia
[4] Yale Univ, Sch Med, Dept Genet, Yale Stem Cell Ctr, New Haven, CT 06520 USA
[5] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
[6] Childrens Hosp, Cell Transplantat Program, Div Pediat Hematol Oncol, Manton Ctr Orphan Dis Res,Howard Hughes Med Inst, Boston, MA 02115 USA
[7] Dana Farber Canc Inst, Boston, MA 02115 USA
来源
DEVELOPMENT | 2011年 / 138卷 / 05期
基金
澳大利亚国家健康与医学研究理事会;
关键词
Endoderm differentiation; Human embryonic stem cells; Human induced pluripotent stem cells; beta-Cell; Pancreas; ISLET-LIKE CLUSTERS; DIRECTED DIFFERENTIATION; PRIMITIVE STREAK; INSULIN; GENERATION; ENDODERM; GENES; REPRESSION; EXPRESSION; MESODERM;
D O I
10.1242/dev.055236
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The generation of insulin-producing beta-cells from human pluripotent stem cells is dependent on efficient endoderm induction and appropriate patterning and specification of this germ layer to a pancreatic fate. In this study, we elucidated the temporal requirements for TGF beta family members and canonical WNT signaling at these developmental stages and show that the duration of nodal/activin A signaling plays a pivotal role in establishing an appropriate definitive endoderm population for specification to the pancreatic lineage. WNT signaling was found to induce a posterior endoderm fate and at optimal concentrations enhanced the development of pancreatic lineage cells. Inhibition of the BMP signaling pathway at specific stages was essential for the generation of insulin-expressing cells and the extent of BMP inhibition required varied widely among the cell lines tested. Optimal stage-specific manipulation of these pathways resulted in a striking 250-fold increase in the levels of insulin expression and yielded populations containing up to 25% C-peptide+cells.
引用
收藏
页码:861 / 871
页数:11
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