CNS synaptogenesis promoted by glia-derived cholesterol
- PMID: 11701931
- DOI: 10.1126/science.294.5545.1354
CNS synaptogenesis promoted by glia-derived cholesterol
Abstract
The molecular mechanisms controlling synaptogenesis in the central nervous system (CNS) are poorly understood. Previous reports showed that a glia-derived factor strongly promotes synapse development in cultures of purified CNS neurons. Here, we identify this factor as cholesterol complexed to apolipoprotein E-containing lipoproteins. CNS neurons produce enough cholesterol to survive and grow, but the formation of numerous mature synapses demands additional amounts that must be provided by glia. Thus, the availability of cholesterol appears to limit synapse development. This may explain the delayed onset of CNS synaptogenesis after glia differentiation and neurobehavioral manifestations of defects in cholesterol or lipoprotein homeostasis.
Comment in
-
Neurobiology. Cholesterol--making or breaking the synapse.Science. 2001 Nov 9;294(5545):1296-7. doi: 10.1126/science.1066724. Science. 2001. PMID: 11701918 No abstract available.
-
Cholesterol's role in synapse formation.Science. 2002 Mar 22;295(5563):2213. doi: 10.1126/science.295.5563.2213a. Science. 2002. PMID: 11911163 No abstract available.
Similar articles
-
Multiple mechanisms mediate cholesterol-induced synaptogenesis in a CNS neuron.Mol Cell Neurosci. 2005 Jun;29(2):190-201. doi: 10.1016/j.mcn.2005.02.006. Mol Cell Neurosci. 2005. PMID: 15911344
-
Role of glia-derived cholesterol in synaptogenesis: new revelations in the synapse-glia affair.J Physiol Paris. 2002 Apr-Jun;96(3-4):257-63. doi: 10.1016/s0928-4257(02)00014-1. J Physiol Paris. 2002. PMID: 12445904 Review.
-
Schwann cells and astrocytes induce synapse formation by spinal motor neurons in culture.Mol Cell Neurosci. 2004 Feb;25(2):241-51. doi: 10.1016/j.mcn.2003.10.011. Mol Cell Neurosci. 2004. PMID: 15019941
-
Glial lipoproteins stimulate axon growth of central nervous system neurons in compartmented cultures.J Biol Chem. 2004 Apr 2;279(14):14009-15. doi: 10.1074/jbc.M313828200. Epub 2004 Jan 6. J Biol Chem. 2004. PMID: 14709547
-
Role of cholesterol in synapse formation and function.Biochim Biophys Acta. 2003 Mar 10;1610(2):271-80. doi: 10.1016/s0005-2736(03)00024-5. Biochim Biophys Acta. 2003. PMID: 12648780 Review.
Cited by
-
A multilevel screening strategy defines a molecular fingerprint of proregenerative olfactory ensheathing cells and identifies SCARB2, a protein that improves regenerative sprouting of injured sensory spinal axons.J Neurosci. 2013 Jul 3;33(27):11116-35. doi: 10.1523/JNEUROSCI.1002-13.2013. J Neurosci. 2013. PMID: 23825416 Free PMC article.
-
Axon growth and synaptic function: A balancing act for axonal regeneration and neuronal circuit formation in CNS trauma and disease.Dev Neurobiol. 2020 Jul;80(7-8):277-301. doi: 10.1002/dneu.22780. Epub 2020 Sep 28. Dev Neurobiol. 2020. PMID: 32902152 Free PMC article. Review.
-
Higher Plasma LDL-Cholesterol is Associated with Preserved Executive and Fine Motor Functions in Parkinson's Disease.Aging Dis. 2016 May 27;7(3):237-45. doi: 10.14336/AD.2015.1030. eCollection 2016 May. Aging Dis. 2016. PMID: 27330838 Free PMC article.
-
The Astrogenic Balance in the Aging Brain.Curr Neuropharmacol. 2021;19(11):1952-1965. doi: 10.2174/1570159X19666210420095118. Curr Neuropharmacol. 2021. PMID: 33881971 Free PMC article. Review.
-
Heart fatty acid-binding protein is associated with phosphorylated tau and longitudinal cognitive changes.Front Aging Neurosci. 2022 Oct 10;14:1008780. doi: 10.3389/fnagi.2022.1008780. eCollection 2022. Front Aging Neurosci. 2022. PMID: 36299612 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical