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10.1007/s12192-017-0790-0

http://scihub22266oqcxt.onion/10.1007/s12192-017-0790-0
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28409327!5425374!28409327
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suck abstract from ncbi


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pmid28409327      Cell+Stress+Chaperones 2017 ; 22 (3): 319-343
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  • Heat shock proteins and kidney disease: perspectives of HSP therapy #MMPMID28409327
  • Chebotareva N; Bobkova I; Shilov E
  • Cell Stress Chaperones 2017[May]; 22 (3): 319-343 PMID28409327show ga
  • Heat shock proteins (HSPs) mediate a diverse range of cellular functions, prominently including folding and regulatory processes of cellular repair. A major property of these remarkable proteins, dependent on intracellular or extracellular location, is their capacity for immunoregulation that optimizes immune activity while avoiding hyperactivated inflammation. In this review, recent investigations are described, which examine roles of HSPs in protection of kidney tissue from various traumatic influences and demonstrate their potential for clinical management of nephritic disease. The HSP70 class is particularly attractive in this respect due to its multiple protective effects. The review also summarizes current understanding of HSP bioactivity in the pathophysiology of various kidney diseases, including acute kidney injury, diabetic nephropathy, chronic glomerulonephritis, and lupus nephritis-along with other promising strategies for their remediation, such as DNA vaccination.
  • |Chaperonin 60/genetics/metabolism[MESH]
  • |HSP27 Heat-Shock Proteins/genetics/metabolism[MESH]
  • |HSP70 Heat-Shock Proteins/genetics/metabolism[MESH]
  • |HSP90 Heat-Shock Proteins/genetics/metabolism[MESH]
  • |Heat-Shock Proteins/genetics/*metabolism[MESH]
  • |Humans[MESH]
  • |Immunotherapy[MESH]
  • |Kidney Diseases/metabolism/*pathology[MESH]
  • |Kidney/metabolism[MESH]
  • |T-Lymphocytes/cytology/immunology/metabolism[MESH]


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