Defective cholesterol clearance limits remyelination in the aged central nervous system

Author:

Cantuti-Castelvetri Ludovico1234ORCID,Fitzner Dirk15ORCID,Bosch-Queralt Mar1234,Weil Marie-Theres16,Su Minhui1234ORCID,Sen Paromita1ORCID,Ruhwedel Torben7,Mitkovski Miso8ORCID,Trendelenburg George5ORCID,Lütjohann Dieter9ORCID,Möbius Wiebke67ORCID,Simons Mikael1234ORCID

Affiliation:

1. Max Planck Institute of Experimental Medicine, 37075 Göttingen, Germany.

2. Munich Cluster for Systems Neurology (SyNergy), 81377 Munich, Germany.

3. Institute of Neuronal Cell Biology, Technical University Munich, 80805 Munich, Germany.

4. German Center for Neurodegenerative Disease (DZNE), 81377 Munich, Germany.

5. Department of Neurology, University of Göttingen Medical Center, 37075 Göttingen, Germany.

6. Center for Nanoscale Microscopy and Molecular Physiology of the Brain (CNMPB), 37075 Göttingen, Germany.

7. Department of Neurogenetics, Max Planck Institute of Experimental Medicine, 37075 Göttingen, Germany.

8. Light Microscopy Facility, Max Planck Institute of Experimental Medicine, 37075 Göttingen, Germany.

9. Institute for Clinical Chemistry and Clinical Pharmacology, University of Bonn, 53127 Bonn, Germany.

Abstract

Keeping cholesterol at bay A decline in tissue repair is a universal hallmark of aging. The failure to regenerate myelin sheaths in multiple sclerosis lesions contributes to chronic progressive disease and disability. Understanding the cause and preventing this failure is a key goal in regenerative medicine. Cantuti-Castelvetri et al. report that the self-limiting inflammatory response, which is necessary for remyelination to occur, is maladaptive in the central nervous system (CNS) of old mice (see the Perspective by Chen and Popko). Cholesterol-rich myelin debris overwhelmed the efflux capacity of phagocytes, resulting in a transition of free cholesterol into crystals, thereby inducing lysosomal rupture and inflammasome stimulation. Thus, drugs being developed to promote cholesterol clearance in human atherosclerosis lesions may also be good candidates for regenerative medicine in the CNS. Science , this issue p. 684 ; see also p. 635

Funder

EU

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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