Comprehensive RNAi-based screening of human and mouse TLR pathways identifies species-specific preferences in signaling protein use

Jing Sun, Ning Li, Kyu Seon Oh, Bhaskar Dutta, Sharat J. Vayttaden, Bin Lin, Thomas S. Ebert, Dominic De Nardo, Joie Davis, Rustam Bagirzadeh, Nicolas W. Lounsbury, Chandrashekhar Pasare, Eicke Latz, Veit Hornung, Iain D C Fraser

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Toll-like receptors (TLRs) are a major class of pattern recognition receptors, whichmediate the responses of innate immune cells to microbial stimuli. To systematically determine the roles of proteins in canonical TLR signaling pathways, we conducted an RNA interference (RNAi)-based screen in human and mouse macrophages. We observed a pattern of conserved signaling module dependencies across species, but found notable species-specific requirements at the level of individual proteins. Among these, weidentified unexpected differences in the involvement of members of the interleukin-1 receptor-associated kinase (IRAK) family between the human andmouse TLR pathways. Whereas TLR signaling inmousemacrophages depended primarily on IRAK4 and IRAK2, with little or no role for IRAK1, TLR signaling and proinflammatory cytokine production in human macrophages depended on IRAK1, with knockdown of IRAK4 or IRAK2 having less of an effect. Consistent with species-specific roles for these kinases, IRAK4 orthologs failed to rescue signaling in IRAK4-deficient macrophages from the other species, and only mouse macrophages required the kinase activity of IRAK4 to mediate TLR responses. The identification of a critical role for IRAK1 in TLR signaling in humans could potentially explain the association of IRAK1 with several autoimmune diseases. Furthermore, this study demonstrated how systematic screening can be used to identify important characteristics of innate immune responses across species, which could optimize therapeutic targeting to manipulate human TLR-dependent outputs.

Original languageEnglish (US)
Article numberra3
JournalScience Signaling
Volume9
Issue number409
DOIs
StatePublished - Jan 5 2016

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Toll-Like Receptors
RNA Interference
Screening
RNA
Macrophages
Proteins
Innate Immunity
Phosphotransferases
Interleukin-1 Receptor-Associated Kinases
Pattern Recognition Receptors
Autoimmune Diseases
Cytokines

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

Comprehensive RNAi-based screening of human and mouse TLR pathways identifies species-specific preferences in signaling protein use. / Sun, Jing; Li, Ning; Oh, Kyu Seon; Dutta, Bhaskar; Vayttaden, Sharat J.; Lin, Bin; Ebert, Thomas S.; De Nardo, Dominic; Davis, Joie; Bagirzadeh, Rustam; Lounsbury, Nicolas W.; Pasare, Chandrashekhar; Latz, Eicke; Hornung, Veit; Fraser, Iain D C.

In: Science Signaling, Vol. 9, No. 409, ra3, 05.01.2016.

Research output: Contribution to journalArticle

Sun, J, Li, N, Oh, KS, Dutta, B, Vayttaden, SJ, Lin, B, Ebert, TS, De Nardo, D, Davis, J, Bagirzadeh, R, Lounsbury, NW, Pasare, C, Latz, E, Hornung, V & Fraser, IDC 2016, 'Comprehensive RNAi-based screening of human and mouse TLR pathways identifies species-specific preferences in signaling protein use', Science Signaling, vol. 9, no. 409, ra3. https://doi.org/10.1126/scisignal.aab2191
Sun, Jing ; Li, Ning ; Oh, Kyu Seon ; Dutta, Bhaskar ; Vayttaden, Sharat J. ; Lin, Bin ; Ebert, Thomas S. ; De Nardo, Dominic ; Davis, Joie ; Bagirzadeh, Rustam ; Lounsbury, Nicolas W. ; Pasare, Chandrashekhar ; Latz, Eicke ; Hornung, Veit ; Fraser, Iain D C. / Comprehensive RNAi-based screening of human and mouse TLR pathways identifies species-specific preferences in signaling protein use. In: Science Signaling. 2016 ; Vol. 9, No. 409.
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