| Literature DB >> 19075240 |
Asim K Mandal1, Phillip B Jones, Angela M Bair, Peter Christmas, Douglas Miller, Ting-ting D Yamin, Douglas Wisniewski, John Menke, Jilly F Evans, Bradley T Hyman, Brian Bacskai, Mei Chen, David M Lee, Boris Nikolic, Roy J Soberman.
Abstract
Leukotrienes (LTs) are signaling molecules derived from arachidonic acid that initiate and amplify innate and adaptive immunity. In turn, how their synthesis is organized on the nuclear envelope of myeloid cells in response to extracellular signals is not understood. We define the supramolecular architecture of LT synthesis by identifying the activation-dependent assembly of novel multiprotein complexes on the outer and inner nuclear membranes of mast cells. These complexes are centered on the integral membrane protein 5-Lipoxygenase-Activating Protein, which we identify as a scaffold protein for 5-Lipoxygenase, the initial enzyme of LT synthesis. We also identify these complexes in mouse neutrophils isolated from inflamed joints. Our studies reveal the macromolecular organization of LT synthesis.Entities:
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Year: 2008 PMID: 19075240 PMCID: PMC2629249 DOI: 10.1073/pnas.0808211106
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205