Volume 64, Issue 1 pp. 408-416
Full Access

Nerve Regeneration and Cholesterol Reutilization Occur in the Absence of Apolipoproteins E and A-I in Mice

Jeffry F. Goodrum

Corresponding Author

Jeffry F. Goodrum

Brain and Development Research Center,

Department of Pathology,

Address correspondence and reprint requests to Dr. J. F. Goodrum at Department of Pathology, CB# 7525, 409 Brinkhous-Bullitt Building, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, U.S.A.Search for more papers by this author
Thomas W. Bouldin

Thomas W. Bouldin

Department of Pathology,

Search for more papers by this author
Sunny H. Zhang

Sunny H. Zhang

Department of Pathology,

Search for more papers by this author
Nobuyo Maeda

Nobuyo Maeda

Department of Pathology,

Program in Molecular Biology and Biotechnology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, U.S.A.

Search for more papers by this author
Brian Popko

Brian Popko

Brain and Development Research Center,

Department of Biochemistry and Biophysics, and

Program in Molecular Biology and Biotechnology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, U.S.A.

Search for more papers by this author
First published: January 1995
Citations: 35

Abstract

Abstract: Apolipoproteins have been implicated in the salvage and reutilization of myelin cholesterol during Wallerian degeneration and the subsequent nerve regeneration. Current evidence suggests that myelin cholesterol complexes with apolipoproteins E and A-I to form lipoproteins that are taken up via low-density lipoprotein receptors on myelinating Schwann cells. We recently reported, however, that apolipoprotein E is not required for nerve regeneration or reutilization of myelin cholesterol. We have now investigated nerve regeneration and the reutilization of cholesterol in mutant mice deficient in both apolipoproteins E and A-I. Morphologic examination of nerves 4 and 12 weeks after crush injury revealed that regeneration proceeded at a normal rate in the absence of these apolipoproteins. Autoradiography of regenerating nerves indicated that prelabeled myelin lipid was reutilized in the regenerating myelin. 3-Hydroxy-3-methylglutaryl-CoA reductase, the rate-limiting enzyme in cholesterol synthesis, was down-regulated in the regenerating nerves, indicative of cholesterol uptake via lipoproteins. Prelabeled myelin cholesterol was present in lipoprotein fractions isolated from crushed nerves of mutant mice. These data suggest that there is considerable redundancy in the process of cholesterol reutilization within nerve, and that apolipoproteins other than apolipoproteins E and A-I may be involved in the recycling of myelin cholesterol.

Abbreviations used: apo, apolipoprotein; 4-APP, 4-aminopyrazolopyrimidine; HMG-CoA, 3-hydroxy-3-methylglutaryl-CoA; LDL, low-density lipoprotein.

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.