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Interaction Network for TLR1

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Toll-like Receptor Signaling
NF-kappa B Signaling
TREM1 Signaling
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Toll Comparative Pathway

Synonyms: CD281, DKFZp547I0610, DKFZp564I0682, KIAA0012, MGC104956, MGC126311, MGC126312, rsc786, TIL, TLR1, TOLL LIKE RECEPTOR 1

Toll Comparative Pathway

Toll-like receptors (TLR) are mammalian homologues of Drosophila Toll receptors. Drosophila Toll receptors have a duel function that depends upon the mechanism of upstream activation. Toll receptors are activated by the endogenous peptide, Spatzle (Spz). Spatzle is present in the hemolymph as an inactive proSpatzle precursor which becomes an active enzyme after proteolysis. If proSpatzle is cleaved by the maternal serine protease, Easter, it functions in the control of dorsal-ventral axis formation.

Drosophila (insect) Toll receptors and vertebrate Toll-like receptors both function as mediators of innate immunity via the recognition of pathogen-associated molecular patterns (PAMP), a process that depends upon pattern recognition receptor (PRR) function. However, the Toll receptor and Toll-like receptor activation mechanisms are different. The Toll-like receptor family members bind directly to class-specific molecules which transduce the defense signals. Specificity is derived from different isotypes/isoforms of Toll-like receptors, different combinations of TLR monomers and cell-specific effector molecules. Toll signaling depends upon the indirect recognition of an infectious element, and coordinated proteolysis of Spatzle. Insect Toll receptors are activated by Spatzle (Spz) cleavage molecules derived from a family of upstream secreted serine proteases, Spatzle-processing enzymes (SPE). Drosophila Toll innate surveillance is mediated by the Gram-negative binding protein 1 (GNBP1) and members of the peptidoglycan recognition protein (PGRP) family, such as PGRP-SA. PGRP-SA recognizes a proteolytically processed Gram-positive peptidoglycan (muropeptide dimer).


References:

  1. Bischoff, V. et. al. (2004) Function of the drosophila pattern-recognition receptor PGRP-SD in the detection of Gram-positive bacteria. Nat. Immunol. 5, 1175-1180.

  2. Filipe, S.R. et. al. (2005) Requirements of peptidoglycan structure that allow detection by the Drosophila Toll pathway. EMBO Rep. 6, 327-333.

  3. Jang, I.H. et. al. (2006) A Spatzle-processing enzyme required for toll signaling activation in Drosophila innate immunity. Dev. Cell. 10, 45-55.

  4. Weber, A.N. et. al. (2003) Binding of the Drosophila cytokine Spatzle to Toll is direct and establishes signaling. Nat. Immunol. 4, 794-800.

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Content for this page is provided by Dennis R. Conrad, Ph.D., a Life Science industry consultant with over 25 years of experience in the formulation and optimization of cell culture media. Dr. Conrad's email address is biomediaexpert@earthlink.net