Laboratory of Biomedical Embryology, Department of Health, Animal Science and Food Safety, Università degli Studi di Milano, 20133, Milan, Italy.
Department of Veterinary Medicine, University of Sassari, 07100, Sassari, Italy.
Stem Cell Rev Rep. 2019 Feb;15(1):82-92. doi: 10.1007/s12015-018-9862-5.
Phenotype definition is driven by epigenetic mechanisms as well as directly influenced by the cell microenvironment and by biophysical signals deriving from the extracellular matrix. The possibility to interact with the epigenetic signature of an adult mature cell, reversing its differentiated state and inducing a short transient high plasticity window, was previously demonstrated. In parallel, in vitro studies have shown that 3D culture systems, mimicking cell native tissue, exert significant effects on cell behavior and functions. Here we report the production of "PTFE micro-bioreactors" for long-term culture of epigenetically derived high plasticity cells. The system promotes 3D cell rearrangement, global DNA demethylation and elevated transcription of pluripotency markers, that is dependent on WW domain containing transcription regulator 1 (TAZ) nuclear accumulation and SMAD family member 2 (SMAD2) co-shuttling. Our findings demonstrate that the use of 3D culture strategies greatly improves the induction and maintenance of a high plasticity state.
表型定义受表观遗传机制驱动,同时直接受到细胞微环境和细胞外基质产生的生物物理信号的影响。先前已经证明,有可能与成年成熟细胞的表观遗传特征相互作用,逆转其分化状态,并诱导短暂的高可塑性窗口。与此同时,体外研究表明,模拟细胞天然组织的 3D 培养系统对细胞行为和功能有显著影响。在这里,我们报告了用于长期培养具有表观遗传衍生高可塑性细胞的“PTFE 微生物反应器”的生产。该系统促进 3D 细胞重排、全基因组 DNA 去甲基化和多能性标记物的转录升高,这依赖于含有 WW 结构域的转录调节因子 1(TAZ)核积累和 SMAD 家族成员 2(SMAD2)共穿梭。我们的研究结果表明,使用 3D 培养策略可极大地提高诱导和维持高可塑性状态的效率。