This Article Full Text Full Text (PDF) Supplemental material Other Versions of this Article: MCB.01824-06v1 27/1/44    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Mack, J. T. Articles by Tew, K. D. Search for Related Content PubMed PubMed Citation Articles by Mack, J. T. Articles by Tew, K. D.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, January 2007, p. 44-53, Vol. 27, No. 1
0270-7306/07/$08.00+0     doi:10.1128/MCB.01824-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

"Skittish" Abca2 Knockout Mice Display Tremor, Hyperactivity, and Abnormal Myelin Ultrastructure in the Central Nervous System ^,

Department of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, 173 Ashley Avenue, P.O. Box 250505, Charleston, South Carolina 29425,¹ Department of Neurology, University of California Davis School of Medicine, and Shriners Hospitals for Children—Northern California, 2425 Stockton Boulevard, Sacramento, California 95817,² Department of Pharmaceutical Sciences, Medical University of South Carolina, 280 Calhoun Street, Charleston, South Carolina 29425³

Received 26 September 2006/ Accepted 12 October 2006

The ATP-binding cassette transporter 2 (ABCA2) is an endolysosomal protein most highly expressed in the central and peripheral nervous system tissues and macrophages. Previous studies indicated its role in cholesterol/steroid (estramustine, estradiol, and progesterone) trafficking/sequestration, oxidative stress response, and Alzheimer's disease. Developmental studies have shown its expression during macrophage and oligodendrocyte differentiation, processes requiring membrane growth. To determine the in vivo function(s) of this transporter, we generated a knockout mouse from a gene-targeted disruption of the murine ABCA2 gene. Knockout males and females are viable and fertile. However, a non-Mendelian inheritance pattern was shown among male progeny of heterozygous crosses. Compared to wild-type and heterozygous littermates, knockout mice displayed a tremor without ataxia, hyperactivity, and reduced body weight; the latter two phenotypes were more marked in females than in males. This sexual disparity suggests a role for ABCA2 in hormone-dependent neurological and/or developmental pathways. Myelin sheath thickness in the spinal cords of knockout mice was greatly increased compared to that in wild-type mice, while a significant reduction in myelin membrane periodicity (compaction) was observed in both spinal cords and cerebra of knockout mice. Loss of ABCA2 function in vivo resulted in abnormal myelin compaction in spinal cord and cerebrum, an ultrastructural defect that we propose to be the cause of the phenotypic tremor.

Published ahead of print on 23 October 2006.

Supplemental material for this article may be found at http://mcb.asm.org/.

This article has been cited by other articles:

• Sakai, H., Tanaka, Y., Tanaka, M., Ban, N., Yamada, K., Matsumura, Y., Watanabe, D., Sasaki, M., Kita, T., Inagaki, N. (2007). ABCA2 Deficiency Results in Abnormal Sphingolipid Metabolism in Mouse Brain. J. Biol. Chem. 282: 19692-19699 [Abstract] [Full Text]