Literature DB >> 27934691

Dead Cert: Measuring Cell Death.

Lisa C Crowley1, Brooke J Marfell1, Adrian P Scott1, Jeanne A Boughaba1,2, Grace Chojnowski3, Melinda E Christensen1,3,4, Nigel J Waterhouse1,3,5.   

Abstract

Many cells in the body die at specific times to facilitate healthy development or because they have become old, damaged, or infected. Defects in cells that result in their inappropriate survival or untimely death can negatively impact development or contribute to a variety of human pathologies, including cancer, AIDS, autoimmune disorders, and chronic infection. Cell death may also occur following exposure to environmental toxins or cytotoxic chemicals. Although this is often harmful, it can be beneficial in some cases, such as in the treatment of cancer. The ability to objectively measure cell death in a laboratory setting is therefore essential to understanding and investigating the causes and treatments of many human diseases and disorders. Often, it is sufficient to know the extent of cell death in a sample; however, the mechanism of death may also have implications for disease progression, treatment, and the outcomes of experimental investigations. There are a myriad of assays available for measuring the known forms of cell death, including apoptosis, necrosis, autophagy, necroptosis, anoikis, and pyroptosis. Here, we introduce a range of assays for measuring cell death in cultured cells, and we outline basic techniques for distinguishing healthy cells from apoptotic or necrotic cells-the two most common forms of cell death. We also provide personal insight into where these assays may be useful and how they may or may not be used to distinguish apoptotic cell death from other death modalities.
© 2016 Cold Spring Harbor Laboratory Press.

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Year:  2016        PMID: 27934691     DOI: 10.1101/pdb.top070318

Source DB:  PubMed          Journal:  Cold Spring Harb Protoc        ISSN: 1559-6095


  22 in total

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2.  Glutamine Maintains Satellite Glial Cells Growth and Survival in Culture.

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Journal:  J Nat Med       Date:  2021-07-21       Impact factor: 2.343

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9.  LncRNA LINC00689 Promotes the Tumorigenesis of Glioma via Mediation of miR-526b-3p/IGF2BP1 Axis.

Authors:  Wen-Liang Zhan; Ning Gao; Guo-Long Tu; Hong Tang; Ling Gao; Ying Xia
Journal:  Neuromolecular Med       Date:  2021-01-03       Impact factor: 3.843

10.  ARA-linker-TGFαL3: a novel chimera protein to target breast cancer cells.

Authors:  Abdolamir Ghadaksaz; Abbas Ali Imani Fooladi; Hamideh Mahmoodzadeh Hosseini; Taher Nejad Satari; Mohsen Amin
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