4.6 Article

Protein Kinase D1 Is Essential for MyD88-Dependent TLR Signaling Pathway

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JOURNAL OF IMMUNOLOGY
卷 182, 期 10, 页码 6316-6327

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0804239

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  1. Children's Foundation Research Center at Le Bonheur Children's Medical Center
  2. National Institutes of Health [AI053137]
  3. Children's Foundation of Memphis
  4. Le Bonheur Children's Medical Center

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Protein kinase D1 (PKD1) has been shown to be involved in certain MAPK activation and cytokine expression by several TLR ligands. However, the precise physiological role of PKD1 in individual signaling from TLRs has not been fully addressed. In this study, we provide evidence that PKD1 is being activated by TLR ligands, except the TLR3 ligand. PKD1 activation by TLR ligands is dependent on MyD88, IL-1R-associated kinase 4 and 1, but independent of TNF-alpha receptor-associated factor 6. PKD1-knock-down macrophages and bone marrow-derived dendritic cells revealed that PKD1 is indispensable for the MyD88-dependent ubiquitination of TNF-alpha receptor-associated factor 6; activation of TGF-beta-activated kinase 1, MAPKs, and transcription factors; and expression of proinflammatory genes induced by TLR ligands, but is not involved in expression of type I IFNs induced by TLR ligands and TRIF-dependent genes induced by TLR3 and TLR4 ligands. These results demonstrate that PKD1 is essential for MyD88-dependent proinflammatory immune responses. The Journal of Immunology, 2009, 182: 6316-6327.

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