Hammond Timothy G, Allen Patricia L, Gunter Margaret A, Chiang Jennifer, Giaever Guri, Nislow Corey, Birdsall Holly H
1Durham VA Medical Center, Medicine Service Line, 508 Fulton Street, Durham, NC 27705 USA.
2Nephrology Division, Department of Medicine, Duke University School of Medicine, Durham, NC 27710 USA.
Microgravity Sci Technol. 2018;30(3):195-208. doi: 10.1007/s12217-017-9588-z. Epub 2017 Dec 29.
Baker's yeast () has broad genetic homology to human cells. Although typically grown as 1-2mm diameter colonies under certain conditions yeast can form very large (10 + mm in diameter) or 'giant' colonies on agar. Giant yeast colonies have been used to study diverse biomedical processes such as cell survival, aging, and the response to cancer pharmacogenomics. Such colonies evolve dynamically into complex stratified structures that respond differentially to environmental cues. Ammonia production, gravity driven ammonia convection, and shear defense responses are key differentiation signals for cell death and reactive oxygen system pathways in these colonies. The response to these signals can be modulated by experimental interventions such as agar composition, gene deletion and application of pharmaceuticals. In this study we used physical factors including colony rotation and microgravity to modify ammonia convection and shear stress as environmental cues and observed differences in the responses of both ammonia dependent and stress response dependent pathways We found that the effects of random positioning are distinct from rotation. Furthermore, both true and simulated microgravity exacerbated both cellular redox responses and apoptosis. These changes were largely shear-response dependent but each model had a unique response signature as measured by shear stress genes and the promoter set which regulates them These physical techniques permitted a graded manipulation of both convection and ammonia signaling and are primed to substantially contribute to our understanding of the mechanisms of drug action, cell aging, and colony differentiation.
贝克酵母()与人类细胞具有广泛的基因同源性。尽管在某些条件下酵母通常以直径1 - 2毫米的菌落形式生长,但在琼脂上酵母可以形成非常大的(直径10毫米以上)或“巨型”菌落。巨型酵母菌落已被用于研究各种生物医学过程,如细胞存活、衰老以及对癌症药物基因组学的反应。这些菌落会动态演变成复杂的分层结构,对环境线索有不同的反应。氨的产生、重力驱动的氨对流以及剪切防御反应是这些菌落中细胞死亡和活性氧系统途径的关键分化信号。对这些信号的反应可以通过实验干预来调节,如琼脂成分、基因缺失和药物应用。在本研究中,我们利用包括菌落旋转和微重力在内的物理因素来改变氨对流和剪切应力作为环境线索,并观察了氨依赖途径和应激反应依赖途径反应的差异。我们发现随机定位的影响与旋转不同。此外,真实和模拟微重力都加剧了细胞氧化还原反应和细胞凋亡。这些变化在很大程度上依赖于剪切反应,但每个模型都有独特的反应特征,通过剪切应力基因及其调控的启动子组来衡量。这些物理技术允许对对流和氨信号进行分级操作,并有望极大地促进我们对药物作用机制、细胞衰老和菌落分化的理解。