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The nuclear membrane organization of leukotriene synthesis
Authors:Asim K. Mandal   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
Affiliation:aRenal Unit, Massachusetts General Hospital, Building 149-The Navy Yard, 13th Street, Charlestown, MA 02129; ;bDepartment of Neurology and Alzheimer''s Disease Research Laboratory, Massachusetts General Hospital, Building 114-The Navy Yard, 16th Street, Charlestown MA, 02129; ;cMerck Research Laboratories, Rahway, NJ 07065; and ;dDivision of Rheumatology, Immunology, and Allergy, Brigham and Women''s Hospital, Boston, MA 02115
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.
Keywords:inflammation   multiprotein complex   5-lipoxygenase   5-lipoxygenase-activating protein
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