Genomic and Nongenomic Signaling Induced by 1α,25(OH)₂-Vitamin D₃ Promotes the Recovery of Amyloid-β Phagocytosis by Alzheimer's Disease Macrophages

Article type: Research Article

Authors: Mizwicki, Mathew T.^{a; *} | Menegaz, Danusa^a | Zhang, Jun^b | Barrientos-Durán, Antonio^a | Tse, Stephen^c | Cashman, John R.^d | Griffin, Patrick R.^b | Fiala, Milan^{c; *}

Affiliations: [a] Department of Biochemistry, University of California, Riverside, CA, USA | [b] Department of Molecular Therapeutics, The Scripps Research Institute, Scripps Florida, Jupiter, FL, USA | [c] Department of Medicine, David Geffen School of Medicine at UCLA and VA Greater Los Angeles Healthcare System, Los Angeles, CA, USA | [d] Human BioMolecular Research Institute, San Diego, CA, USA

Correspondence: [*] Correspondence to: Mathew T. Mizwicki (E-mail: [email protected]) or Milan Fiala, UCLA CHS, 650 Charles E. Young Drive South, Room 23-338, Los Angeles, CA 90095-3517, USA. E-mail: [email protected].

Abstract: Brain clearance of amyloid-β (Aβ42) by innate immune cells is necessary for maintenance of normal brain function. Phagocytosis of soluble Aβ42 by Alzheimer's disease (AD) macrophages is defective, recovered in all “Type I and Type II” AD patients by 1α,25(OH)2-vitamin D3 (1,25D3) and blocked by the nuclear vitamin D receptor (VDR) antagonist (23S)-25-dehydro-1α(OH)-vitamin D3-26,23-lactone (MK). Bisdemethoxycurcumin (BDC) is a VDR ligand and additive with 1,25D3 in promoting Aβ42 phagocytosis by Type I, but not by Type II macrophages. Here, we define the following intracellular mechanisms regulated by 1,25D3 that are associated with recovery of phagocytosis and consistent with the selectivity of BDC: 1) 1,25D3 potentiates a 4,4-diisothiocyanostilbene-2,2-disulfonic acid-sensitive chloride channel (i.e., ClC-3) currents in both Type I and II AD macrophages, but curcumin only potentiates the currents in Type I cells; 2) 1,25D3 is particularly effective in upregulating ClC-3 mRNA expression in Type II peripheral blood mononuclear cells (PBMCs) while both 1,25D3 and the BDC analog, C180, upregulate VDR mRNA, repressed by Aβ42 in Type II PBMCs; and 3) 1,25D3-induced Aβ42 phagocytosis is attenuated by the calcium-dependent ClC-3 blocker, inositol 3,4,5,6-tetraphosphate (IP4), in both AD Types and by the MEK1/2 inhibitor U0126 only in Type II macrophages. VDR hydrogen/deuterium exchange coupled mass spectrometry and computational results show differences between the abilities of 1,25D3 and curcuminoids to stabilize VDR helices associated with the regulation of gene transcription. The structure-function results provide evidence that 1,25D3 activation of VDR-dependent genomic and nongenomic signaling, work in concert to recover dysregulated innate immune function in AD.

Keywords: Alzheimer's disease, amyloid-β, chloride channel, ClC-3, curcumin, hydrogen-deuterium exchange, nongenomic, nuclear vitamin D receptor, phagocytosis, 1α25(OH)₂-vitamin D₃

DOI: 10.3233/JAD-2012-110560

Journal: Journal of Alzheimer's Disease, vol. 29, no. 1, pp. 51-62, 2012