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Physiol. Genomics 20: 73-86, 2004. First published October 5, 2004; doi:10.1152/physiolgenomics.00187.2004 Free Article
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Received 16 August 2004; accepted in final form 4 October 2004.
Physiological Genomics 20:73-86 (2004)
1094-8341/04 $5.00 © 2004 American Physiological Society

Target ablation-induced regulation of macrophage recruitment into the olfactory epithelium of Mip-1{alpha}–/– mice and restoration of function by exogenous MIP-1{alpha}

Kevin Kwong1, Radhika A. Vaishnav2, Yushu Liu3, Nishikant Subhedar4, Arnold J. Stromberg3, Marilyn L. Getchell2,4 and Thomas V. Getchell1,4

1 Department of Physiology, University of Kentucky, Lexington, Kentucky
2 Department of Anatomy and Neurobiology, University of Kentucky, Lexington, Kentucky
3 Department of Statistics, University of Kentucky, Lexington, Kentucky
4 Sanders-Brown Center on Aging, University of Kentucky, Lexington, Kentucky

The chemokine macrophage inflammatory protein (MIP)-1{alpha} recruits macrophages to sites of epithelial remodeling. We showed previously that mRNA and protein levels of MIP-1{alpha} in the olfactory epithelium (OE) increased significantly at 3 days after bilateral olfactory bulbectomy (OBX). The first aim of this study was to investigate the effect of the absence of MIP-1{alpha} on macrophage recruitment to the OE 3 days after OBX in Mip-1{alpha}–/– mice compared with C57BL/6 mice and to test whether chemokine function could be restored by MIP-1{alpha} protein injection into Mip-1{alpha}–/– mice. OBX was performed on C57BL/6 and Mip-1{alpha}–/– mice. The mice received six subcutaneous injections at 12-h intervals of either 10 µg/ml MIP-1{alpha} protein in carrier or carrier only. Macrophage recruitment was evaluated with antibodies to CD68 for all macrophages and F4/80 for activated macrophages. Compared with C57BL/6 mice, at 3 days post-OBX the numbers of CD68+ and F4/80+ macrophages were significantly lower in carrier-injected Mip-1{alpha}–/– mice and were comparable in MIP-1{alpha} protein-injected Mip-1{alpha}–/– mice. The second aim was to determine the identity of genes regulated at 3 days post-OBX in the OE of carrier-injected Mip-1{alpha}–/– mice compared with carrier-injected C57BL/6 mice. Total RNA from the OE was hybridized to Affymetrix microarrays. A number of chemokine-, cytokine-, and growth factor-related genes were significantly regulated in the Mip-1{alpha}–/– mice and were restored in MIP-1{alpha} protein-injected Mip-1{alpha}–/– mice. The results illustrated that MIP-1{alpha} played a key role in recruitment of macrophages to the OE and provided insight into the genomic regulation involved in OE remodeling.

macrophage activation; olfactory bulbectomy; globose basal cell; proliferation; microarray




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A. S. Borders, M. A. Hersh, M. L. Getchell, N. van Rooijen, D. A. Cohen, A. J. Stromberg, and T. V. Getchell
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M. L. Getchell, H. Li, R. A. Vaishnav, A. S. Borders, J. Witta, N. Subhedar, W. de Villiers, A. J. Stromberg, and T. V. Getchell
Temporal gene expression profiles of target-ablated olfactory epithelium in mice with disrupted expression of scavenger receptor A: impact on macrophages
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