Immunological consequences of kidney cell death

• Published in: Cell death & disease Vol. 9; no. 2; pp. 114 - 15
• Main Authors: Sarhan, Maysa, von Mässenhausen, Anne, Hugo, Christian, Oberbauer, Rainer, Linkermann, Andreas
• Format: Journal Article
• Language: English
• Published: England Springer Nature B.V 25.01.2018; Nature Publishing Group UK
• Subjects: Apoptosis; Autoimmune diseases; Autoimmunity; Cell death; Cytokines; Ferroptosis; Gangrene; Glomerulonephritis; Graft rejection; Immunogenicity; Immunological memory; Inflammasomes; Inflammation; Interleukin 18; Kidney transplantation; Kidneys; Lymphocytes B; Lysosomes; Memory cells; Mitochondria; Necroptosis; Necrosis; Organelles; Pathophysiology; Peroxisomes; Phagocytosis; Pyroptosis; Review; Rupture; Signal transduction; Therapeutic applications; Transplantation; Transplants & implants
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-017-0057-9

Death of renal cells is central to the pathophysiology of acute tubular necrosis, autoimmunity, necrotizing glomerulonephritis, cystic kidney disease, urosepsis, delayed graft function and transplant rejection. By means of regulated necrosis, immunogenic damage-associated molecular patterns (DAMPs) and highly reactive organelles such as lysosomes, peroxisomes and mitochondria are released from the dying cells, thereby causing an overwhelming immunologic response. The rupture of the plasma membrane exhibits the "point of no return" for the immunogenicity of regulated cell death, explaining why apoptosis, a highly organized cell death subroutine with long-lasting plasma membrane integrity, elicits hardly any immune response. Ferroptosis, an iron-dependent necrotic type cell death, results in the release of DAMPs and large amounts of lipid peroxides. In contrast, anti-inflammatory cytokines are actively released from cells that die by necroptosis, limiting the DAMP-induced immune response to a surrounding microenvironment, whereas at the same time, inflammasome-associated caspases drive maturation of intracellularly expressed interleukin-1β (IL-1β). In a distinct setting, additionally interleukin-18 (IL-18) is expressed during pyroptosis, initiated by gasdermin-mediated plasma membrane rupture. As all of these pathways are druggable, we provide an overview of regulated necrosis in kidney diseases with a focus on immunogenicity and potential therapeutic interventions.