Crowley Lisa C, Waterhouse Nigel J
Apoptosis and Cytotoxicity Laboratory, Mater Research, Translational Research Institute, Woolloongabba, Brisbane, Queensland 4102, Australia;
Apoptosis and Cytotoxicity Laboratory, Mater Research, Translational Research Institute, Woolloongabba, Brisbane, Queensland 4102, Australia; Flow Cytometry and Imaging, QIMR Berghofer Medical Research Institute, Herston, Brisbane, Queensland 4006, Australia; School of Medicine, University of Queensland, St. Lucia, Brisbane, Queensland 4072, Australia.
Cold Spring Harb Protoc. 2016 Aug 1;2016(8):2016/8/pdb.prot087189. doi: 10.1101/pdb.prot087189.
Colony-forming assays measure the ability of cells in culture to grow and divide into groups. Any cell that has the potential to form a colony may also have the potential to cause cancer or relapse in vivo. Colony-forming assays also provide an indirect measurement of cell death because any cell that is dead or dying will not continue to proliferate. The proliferative capacity of adherent cells such as fibroblasts can be determined by growing cells at low density on culture dishes and counting the number of distinct groups that form over time. Cells that grow in suspension, such as hematopoietic cells, cannot be assayed this way because the cells move freely in the media. Assays to determine the colony-forming ability of hematopoietic cells must therefore be performed in solid matrices that restrict large-scale movement of the cells. One such matrix is soft agar. This protocol describes the use of soft agar to compare the colony-forming ability of untreated hematopoietic cells to the colony-forming ability of hematopoietic cells that have been treated with a cytotoxic agent.
集落形成试验用于测定培养中的细胞生长并分裂成细胞群的能力。任何具有形成集落潜力的细胞在体内也可能具有引发癌症或复发的潜力。集落形成试验还能间接测量细胞死亡情况,因为任何已经死亡或正在死亡的细胞都不会继续增殖。诸如成纤维细胞等贴壁细胞的增殖能力可通过在培养皿中低密度培养细胞并计数随时间形成的不同细胞群数量来确定。悬浮生长的细胞,如造血细胞,无法用这种方法进行检测,因为细胞在培养基中可自由移动。因此,测定造血细胞集落形成能力的试验必须在能限制细胞大规模移动的固体基质中进行。一种这样的基质就是软琼脂。本方案描述了使用软琼脂来比较未处理的造血细胞与经细胞毒性剂处理的造血细胞的集落形成能力。