RACK1 and NEK7 mediate GSDMD-dependent macrophage pyroptosis upon Streptococcus suis infection

Vet Res. 2024 Sep 27;55(1):120. doi: 10.1186/s13567-024-01376-w.

Abstract

Streptococcus suis serotype 2 (SS2) is an important zoonotic pathogen that induces an NLRP3-dependent cytokine storm. NLRP3 inflammasome activation triggers not only an inflammatory response but also pyroptosis. However, the exact mechanism underlying S. suis-induced macrophage pyroptosis is not clear. Our results showed that SS2 induced the expression of pyroptosis-associated factors, including lactate dehydrogenase (LDH) release, propidium iodide (PI) uptake and GSDMD-N expression, as well as NLRP3 inflammasome activation and IL-1β secretion. However, GSDMD deficiency and NLRP3 inhibition using MCC950 attenuated the SS2-induced expression of pyroptosis-associated factors, suggesting that SS2 induces NLRP3-GSDMD-dependent pyroptosis. Furthermore, RACK1 knockdown also reduced the expression of pyroptosis-associated factors. In addition, RACK1 knockdown downregulated the expression of NLRP3 and Pro-IL-1β as well as the phosphorylation of P65. Surprisingly, the interaction between RACK1 and P65 was detected by co-immunoprecipitation, indicating that RACK1 induces macrophage pyroptosis by mediating the phosphorylation of P65 to promote the transcription of NLRP3 and pro-IL-1β. Similarly, NEK7 knockdown decreased the expression of pyroptosis-associated factors and ASC oligomerization. Moreover, the results of co-immunoprecipitation revealed the interaction of NEK7-RACK1-NLRP3 during SS2 infection, demonstrating that NEK7 mediates SS2-induced pyroptosis via the regulation of NLRP3 inflammasome assembly and activation. These results demonstrate the important role of RACK1 and NEK7 in SS2-induced pyroptosis. Our study provides new insight into SS2-induced cell death.

Keywords: Streptococcus suis; GSDMD; NEK7; NLRP3 inflammasome; RACK1; pyroptosis.

MeSH terms

  • Animals
  • Gasdermins
  • Inflammasomes / genetics
  • Inflammasomes / metabolism
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Macrophages* / metabolism
  • Macrophages* / microbiology
  • Mice
  • Mice, Inbred C57BL
  • NIMA-Related Kinases* / genetics
  • NIMA-Related Kinases* / metabolism
  • Phosphate-Binding Proteins / genetics
  • Phosphate-Binding Proteins / metabolism
  • Pyroptosis*
  • Receptors for Activated C Kinase* / genetics
  • Receptors for Activated C Kinase* / metabolism
  • Streptococcal Infections* / immunology
  • Streptococcal Infections* / microbiology
  • Streptococcal Infections* / veterinary
  • Streptococcus suis* / physiology

Substances

  • NIMA-Related Kinases
  • Receptors for Activated C Kinase
  • Nek7 protein, mouse
  • Gsdmd protein, mouse
  • Phosphate-Binding Proteins
  • Intracellular Signaling Peptides and Proteins
  • Inflammasomes
  • Gasdermins