A Multifunctional 3D Co-Culture System for Studies of Mammary Tissue Morphogenesis and Stem Cell Biology

被引:83
作者
Campbell, Jonathan J. [1 ]
Davidenko, Natalia [2 ]
Caffarel, Maria M. [1 ]
Cameron, Ruth E. [2 ]
Watson, Christine J. [1 ]
机构
[1] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[2] Univ Cambridge, Dept Mat Sci & Met, Cambridge CB2 3QZ, England
基金
英国生物技术与生命科学研究理事会;
关键词
BRANCHING MORPHOGENESIS; HYALURONAN; CD44; EXPRESSION; GLYCOSAMINOGLYCANS; ORGANIZATION; ADHESION; KINASE;
D O I
10.1371/journal.pone.0025661
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Studies on the stem cell niche and the efficacy of cancer therapeutics require complex multicellular structures and interactions between different cell types and extracellular matrix (ECM) in three dimensional (3D) space. We have engineered a 3D in vitro model of mammary gland that encompasses a defined, porous collagen/hyaluronic acid (HA) scaffold forming a physiologically relevant foundation for epithelial and adipocyte co-culture. Polarized ductal and acinar structures form within this scaffold recapitulating normal tissue morphology in the absence of reconstituted basement membrane (rBM) hydrogel. Furthermore, organoid developmental outcome can be controlled by the ratio of collagen to HA, with a higher HA concentration favouring acinar morphological development. Importantly, this culture system recapitulates the stem cell niche as primary mammary stem cells form complex organoids, emphasising the utility of this approach for developmental and tumorigenic studies using genetically altered animals or human biopsy material, and for screening cancer therapeutics for personalised medicine.
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页数:9
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