Purinergic signaling in leishmaniasis infection

Summary
Organism
Homo sapiens (human)
Reactome
R-HSA-9660826
PubChem
R-HSA-9660826
Description
  • The purinoreceptors are divided into inotropic (P2XR) and metabotropic (P2YR) subtypes whose ligands are the nucleotides ATP and UDP respectively (Cekic et al. 2016). The binding of these nucleotides to their receptors on macrophages have been associated with the activation of the inflammasome leading to the subsequent activation of interleukin 1 beta (IL1β) and TNF-α (Cekic et al. 2016 & Figueiredo et al. 2016). The liberation of ATP comes from tissues facing stressful stimuli such as a tissue injury or microorganism infection, amongst others. As a regulatory mechanism, certain enzymes can reduce ATP to Adenosine and a nucleoside can stimulate signalling pathways leading to the synthesis of anti-inflammatory cytokines (Cekic et al. 2016).

    The activation of the receptor P2RX7 was shown to lead to the activation of killing mechanisms or cell death programs, ending up in the elimination of microbes such as Leishmania amazonensis, Mycobacterium tuberculosis, Chlamydia psittaci, and Toxoplasma gondii (Coutinho-Silva et al. 2012 & Idzko, 2014).
Click on a node on the pathway to see its details. Glycoproteins are marked with a glycoprotein icon in their name.
Displaying entries 1 - 10 of 18 in total
UniProt ID Protein Name Gene Symbol Pathway Viewer
O15553 Pyrin
  • MEF
  • MEFV
  • TRIM20
view
O43586 Proline-serine-threonine phosphatase-interacting protein 1
  • CD2BP1
  • PSTPIP1
view
O75356 Nucleoside diphosphate phosphatase ENTPD5
  • CD39L4
  • ENTPD5
  • PCPH
view
P01024 Complement C3
  • C3
  • CPAMD1
  • HEL-S-62p
view
P01583 Interleukin-1 alpha
  • IL1A
  • IL1F1
view
P05067 Amyloid-beta precursor protein
  • A4
  • AD1
  • APP
view
P08238 Heat shock protein HSP 90-beta
  • HSP90AB1
  • HSP90B
  • HSPC2
  • HSPC3
  • HSPCB
view
P08311 Cathepsin G
  • CTSG
view
P19838 Nuclear factor NF-kappa-B p105 subunit
  • NFKB1
view
P21589 5'-nucleotidase
  • NT5
  • NT5E
  • NTE
view

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026