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      Molecular mechanisms of natural killer cell activation in response to cellular stress.

      1 , ,
      Cell death and differentiation

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          Abstract

          Protection against cellular stress from various sources, such as nutritional, physical, pathogenic, or oncogenic, results in the induction of both intrinsic and extrinsic cellular protection mechanisms that collectively limit the damage these insults inflict on the host. The major extrinsic protection mechanism against cellular stress is the immune system. Indeed, it has been well described that cells that are stressed due to association with viral infection or early malignant transformation can be directly sensed by the immune system, particularly natural killer (NK) cells. Although the ability of NK cells to directly recognize and respond to stressed cells is well appreciated, the mechanisms and the breadth of cell-intrinsic responses that are intimately linked with their activation are only beginning to be uncovered. This review will provide a brief introduction to NK cells and the relevant receptors and ligands involved in direct responses to cellular stress. This will be followed by an in-depth discussion surrounding the various intrinsic responses to stress that can naturally engage NK cells, and how therapeutic agents may induce specific activation of NK cells and other innate immune cells by activating cellular responses to stress.

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          Author and article information

          Journal
          Cell Death Differ.
          Cell death and differentiation
          1476-5403
          1350-9047
          Jan 2014
          : 21
          : 1
          Affiliations
          [1 ] 1] Cellular Immunity Laboratory, Cancer Immunology Program, Trescowthick Research Laboratories, Peter MacCallum Cancer Centre, East Melbourne, Australia [2] Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, Australia [3] Department of Immunology, Monash University, AMREP, Prahran, Australia.
          Article
          cdd201326
          10.1038/cdd.2013.26
          23579243
          b7a44445-d50f-414a-ab03-8ab5ed008634
          History

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