COVID-19 and endothelial cell senescence (Homo sapiens)

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PPP87771713881013, 17131788105, 12, 169109EndosomeSARS-CoV 2SARS-CoV 2PISRESARS-CoV 2 RNATLR3TRIFTLR2IRAK4TLR9MAVSTREML4 Innate ImmunityMDA5 RIG-I (DDX58)GRL0617108NucleusIKBKEIRF3TRAF6MYD88TRAF3TBK1JAK1OAS1PKR88PLpro (nsp3)178174, 14IFNAR1IFNAR2TYK28STAT1STAT2IRF9INF-I alpha/ betaISREISGs8OAS2OAS3nsp13virus proteinACE2SARS-CoV 2TLR7TLR6TLR4MYD88101010NFkB10Pro-inflammatory cytokines production1010101013, 1713, 1713, 1710, 17IRF3IRF7PPIRF3IRF3INF-I alpha/ beta10, 17SARS-CoV 2 RNA10101010ACE2INF-I alpha/ betansp1STAT1STAT213nsp1nsp1013nsp14nsp15nsp161313131313131313ORF3aORF61313azithromycin21, 36, 11, 15


Description

The induction of Type I interferons and signaling is the first response leading to the innate immune reactions during SARS-COV-2 infection. The virus can enter host cells through two mechanisms. If it enters the cell via diffusion mediated by TMPRSS2, the virus ssRNA will be detected by RIG-I and MDA5 in the cytosol. If the virus enters the cell via endocytosis, the spike proteins will be processed by CTSL in the lysosome leading to the detection of ssRNA by TLR3,7 and 9 (PMID 33506952). The extracellular virus can also be detected by TLR2,4 and 6 (PMID 33506952). The higher production of TLR4 in men and the presence of TLR7 on the X chromosome may contribute to the different responses between women and men during SARS-CoV 2 infection (PMID 33506952). TLR7 MYD88-dependent signaling is inhibited at multiple steps by the SARS-CoV Papain-Like Protease (PLpro) domain of nsp3 (red oval). The signaling pathway is critical to induction of type I interferons (INF-I) via IRF3, AP-1 and NFkB transcription factors. INF-I triggers the JAK/STAT pathway leading to the induction of interferon-stimulated genes (ISGs), such as OAS and PKR, which go one to conduct the innate immune response. TREML4 has been shown to be necessary for MYD88 recruitment by TLR7 and STAT1 participation. The inhibition of SARS-CoV-2 PLpro by GRL0617 is proposed based on Ratia, et al. 2008 and 100% sequence identity between SARS-CoV and SARS-CoV-2 across all 13 residues of PLpro involved in binding GRL0617 (82.9% identity across 316 amino acids) as determined by the alignment of RefSeq YP_009725299.1 and PDB 3E9S (https://alexanderpico.github.io/SARS-CoV-2_Alignments/#Nsp3_PLpro_domain). The antimicrobial agent, azithromycin, is in clincal trials as COVID-19 therapy in combination with hydroxychloroquine (Gautret 2020) has been shown to modulate inflammation by inhibiting the activation of many of these same transcription factors.

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Bibliography

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History

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CompareRevisionActionTimeUserComment
124640view12:48, 18 November 2022Jfigueirahasbunupdated viral protein labels, shapes and identifiers
124554view12:38, 8 November 2022EweitzReduce negative space at top and left of pathway graphic
124553view12:32, 8 November 2022EweitzUse name instead of ID as pathway label, fix typos, refine virus dimensions
124552view12:25, 8 November 2022EweitzModified title
124041view15:07, 14 September 2022DeSlUpdate ID for NSP4
124040view15:05, 14 September 2022DeSlChnaged MIM-conversion to Arrows
124039view15:04, 14 September 2022DeSlConverted SARS-COV2 drawing to graphical lines
123978view10:43, 9 September 2022EweitzModified title
123678view09:52, 9 August 2022EgonwNot a mim-conversion
123532view06:33, 2 August 2022EgonwMade a pathway clickable
123236view14:51, 5 July 2022LaureAlix
123235view14:48, 5 July 2022LaureAlix
123222view14:21, 5 July 2022LaureAlixModified description
123221view14:20, 5 July 2022LaureAlix
123220view14:10, 5 July 2022LaureAlix
123217view14:06, 5 July 2022LaureAlix
123215view14:03, 5 July 2022LaureAlixchanges
123209view13:39, 5 July 2022LaureAlix
123208view13:38, 5 July 2022LaureAlixNew pathway

External references

DataNodes

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NameTypeDatabase referenceComment
ACE2GeneProductQ9BYF1 (Uniprot-TrEMBL)
GRL0617MetaboliteQ27097846 (Wikidata)
IFNAR1GeneProductENSG00000142166 (Ensembl)
IFNAR2GeneProductENSG00000159110 (Ensembl)
IKBKEGeneProductENSG00000263528 (Ensembl)
INF-I alpha/ betaProteinQ6046488 (Wikidata)
IRAK4ProteinENSG00000198001 (Ensembl)
IRF3GeneProductENSG00000126456 (Ensembl)
IRF7GeneProductENSG00000185507 (Ensembl)
IRF9GeneProductENSG00000213928 (Ensembl)
ISGsProtein
Innate ImmunityPathway
JAK1GeneProductENSG00000162434 (Ensembl)
MAVSProteinENSG00000088888 (Ensembl)
MDA5 ProteinENSG00000115267 (Ensembl)
MYD88GeneProductENSG00000172936 (Ensembl)
OAS1GeneProductENSG00000089127 (Ensembl)
OAS2GeneProductENSG00000111335 (Ensembl)
OAS3GeneProductENSG00000111331 (Ensembl)
ORF3aProteinP0DTC3 (Uniprot-TrEMBL) PDB structure for SARS-CoV strain: 6JYT
ORF6ProteinP0DTC6 (Uniprot-TrEMBL) PDB structure for SARS-CoV strain: 6JYT
PKRGeneProductENSG00000055332 (Ensembl)
PLpro (nsp3)ProteinYP_009725299.1 (RefSeq)
Pro-inflammatory cytokines productionPathway
RIG-I (DDX58)ProteinENSG00000107201 (Ensembl)
SARS-CoV 2 RNARnaQ82069695 (Wikidata)
STAT1GeneProductENSG00000115415 (Ensembl)
STAT2GeneProductENSG00000170581 (Ensembl)
TBK1GeneProductENSG00000183735 (Ensembl)
TLR2ProteinO60603 (Uniprot-TrEMBL)
TLR3ProteinO15455 (Uniprot-TrEMBL)
TLR4ProteinO00206 (Uniprot-TrEMBL)
TLR6ProteinQ9Y2C9 (Uniprot-TrEMBL)
TLR7GeneProductENSG00000196664 (Ensembl)
TLR9ProteinQ9NR96 (Uniprot-TrEMBL)
TRAF3GeneProductENSG00000131323 (Ensembl)
TRAF6GeneProductENSG00000175104 (Ensembl)
TREML4 ProteinQ6UXN2 (Uniprot-TrEMBL)
TRIF Protein
TYK2GeneProductENSG00000105397 (Ensembl)
azithromycinMetaboliteQ165399 (Wikidata)
nsp10ProteinYP_009725306 (NCBI Protein) PDB structure for SARS-CoV strain: 6JYT
nsp13ProteinQII57165.1 (RefSeq) PDB structure for SARS-CoV strain: 6JYT
nsp14ProteinYP_009725309 (NCBI Protein) PDB structure for SARS-CoV strain: 6JYT
nsp15ProteinYP_009725310 (NCBI Protein) PDB structure for SARS-CoV strain: 6JYT
nsp16ProteinYP_009725311 (NCBI Protein) PDB structure for SARS-CoV strain: 6JYT
nsp1ProteinYP_009725297 (NCBI Protein) PDB structure for SARS-CoV strain: 6JYT

Annotated Interactions

No annotated interactions

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