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10.1007/s12016-020-08824-3

http://scihub22266oqcxt.onion/10.1007/s12016-020-08824-3
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suck abstract from ncbi


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pmid33405100      Clin+Rev+Allergy+Immunol 2021 ; 60 (2): 271-292
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  • New Insights on the Role of TRP Channels in Calcium Signalling and Immunomodulation: Review of Pathways and Implications for Clinical Practice #MMPMID33405100
  • Froghi S; Grant CR; Tandon R; Quaglia A; Davidson B; Fuller B
  • Clin Rev Allergy Immunol 2021[Apr]; 60 (2): 271-292 PMID33405100show ga
  • Calcium is the most abundant mineral in the human body and is central to many physiological processes, including immune system activation and maintenance. Studies continue to reveal the intricacies of calcium signalling within the immune system. Perhaps the most well-understood mechanism of calcium influx into cells is store-operated calcium entry (SOCE), which occurs via calcium release-activated channels (CRACs). SOCE is central to the activation of immune system cells; however, more recent studies have demonstrated the crucial role of other calcium channels, including transient receptor potential (TRP) channels. In this review, we describe the expression and function of TRP channels within the immune system and outline associations with murine models of disease and human conditions. Therefore, highlighting the importance of TRP channels in disease and reviewing potential. The TRP channel family is significant, and its members have a continually growing number of cellular processes. Within the immune system, TRP channels are involved in a diverse range of functions including T and B cell receptor signalling and activation, antigen presentation by dendritic cells, neutrophil and macrophage bactericidal activity, and mast cell degranulation. Not surprisingly, these channels have been linked to many pathological conditions such as inflammatory bowel disease, chronic fatigue syndrome and myalgic encephalomyelitis, atherosclerosis, hypertension and atopy.
  • |Animals[MESH]
  • |Autoimmunity[MESH]
  • |B-Lymphocytes/*immunology[MESH]
  • |Cell Degranulation[MESH]
  • |Humans[MESH]
  • |Lymphocyte Activation[MESH]
  • |Mast Cells/*immunology[MESH]
  • |Mice[MESH]
  • |Neutrophils/*immunology[MESH]
  • |Signal Transduction[MESH]
  • |T-Lymphocytes/*immunology[MESH]


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