Differentiation of Human Induced Pluripotent Stem Cells to Mammary-like Organoids

被引:56
|
作者
Qu, Ying [1 ]
Han, Bingchen [1 ]
Gao, Bowen [1 ]
Bose, Shikha [2 ]
Gong, Yiping [3 ]
Wawrowsky, Kolja [4 ]
Giuliano, Armando E. [1 ]
Sareen, Dhruv [4 ,5 ,6 ]
Cui, Xiaojiang [1 ]
机构
[1] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Dept Surg, 8700 Beverly Blvd,Davis Bldg 2065, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Dept Pathol, Los Angeles, CA 90048 USA
[3] Hubei Canc Hosp, Dept Breast Surg, Wuhan 430079, Peoples R China
[4] Cedars Sinai Med Ctr, Dept Biomed Sci, Los Angeles, CA 90048 USA
[5] Cedars Sinai Med Ctr, Board Governors Regenerat Med Inst, Los Angeles, CA 90048 USA
[6] Cedars Sinai Med Ctr, David & Janet Polak Fdn Stem Cell Core Lab, Los Angeles, CA 90048 USA
来源
STEM CELL REPORTS | 2017年 / 8卷 / 02期
关键词
GLAND DEVELOPMENT; HUMAN BREAST; BRANCHING MORPHOGENESIS; DUCTAL MORPHOGENESIS; EXTRACELLULAR-MATRIX; EPITHELIAL-CELLS; PROGENITOR CELLS; KEY STAGES; KAPPA-B; GENERATION;
D O I
10.1016/j.stemcr.2016.12.023
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human induced pluripotent stem cells (iPSCs) can give rise to multiple cell types and hold great promise in regenerative medicine and disease-modeling applications. We have developed a reliable two-step protocol to generate human mammary-like organoids from iPSCs. Non-neural ectoderm-cell-containing spheres, referred to as mEBs, were first differentiated and enriched from iPSCs using MammoCult medium. Gene expression profile analysis suggested that mammary gland function-associated signaling pathways were hallmarks of 10day differentiated mEBs. We then generated mammary-like organoids from 10-day mEBs using 3D floating mixed gel culture and a threestage differentiation procedure. These organoids expressed common breast tissue, luminal, and basal markers, including estrogen receptor, and could be induced to produce milk protein. These results demonstrate that human iPSCs can be directed in vitro toward mammary lineage differentiation. Our findings provide an iPSC-based model for studying regulation of normal mammary cell fate and function as well as breast disease development.
引用
收藏
页码:205 / 215
页数:11
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