シナプトソーム
- 関
- synaptosomal
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2017/04/14 18:05:05」(JST)
[Wiki en表示]
Synaptosome |
Schematic of isolated synaptosome with numerous small synaptic vesicles, two dense-core vesicles, one mitochondrion and a patch of postsynaptic membrane attached to the presynaptic active zone
|
Details |
Identifiers |
Greek |
synapto-soma |
MeSH |
Synaptosomes |
Code |
TH H2.00.06.2.00033 |
Anatomical terminology
[edit on Wikidata]
|
A synaptosome is an isolated synaptic terminal from a neuron. Synaptosomes are obtained by mild homogenization of nervous tissue under isotonic conditions and subsequent fractionation using differential and density gradient centrifugation. Liquid shear detaches the nerve terminals from the axon and the plasma membrane surrounding the nerve terminal particle reseals. Synaptosomes are osmotically sensitive, contain numerous small clear synaptic vesicles, sometimes larger dense-core vesicles and frequently one or more small mitochondria. They carry the morphological features and most of the chemical properties of the original nerve terminal. Synaptosomes isolated from mammalian brain often retain a piece of the attached postsynaptic membrane, facing the active zone.
Synaptosomes were first isolated in an attempt to identify the subcellular compartment corresponding to the fraction of so-called bound acetylcholine that remains when brain tissue is homogenized in iso-osmotic sucrose. Particles containing acetylcholine and its synthesizing enzyme choline acetyltransferase were originally isolated by Hebb and Whittaker (1958)[1] at the Agricultural Research Council, Institute of Animal Physiology, Babraham, Cambridge, UK. In a collaborative study with the electron microscopist George Gray from University College London, Victor P. Whittaker eventually showed that the acetylcholine-rich particles derived from guinea-pig cerebral cortex were synaptic vesicle-rich pinched-off nerve terminals.[2][3] Whittaker coined the term synaptosome to describe these fractionation-derived particles and shortly thereafter synaptic vesicles could be isolated from lysed synaptosomes.[4][5]
Synaptosomes are commonly used to study synaptic transmission in the test tube because they contain the molecular machinery necessary for the uptake, storage, and release of neurotransmitters. In addition they have become a common tool for drug testing. They maintain a normal membrane potential, contain presynaptic receptors, translocate metabolites and ions, and when depolarized, release multiple neurotransmitters (including acetylcholine, amino acids, catecholamines, and peptides) in a Ca2+-dependent manner. Synaptosomes isolated from the whole brain or certain brain regions are also useful models for studying structure-function relationships in synaptic vesicle release.[6] Synaptosomes can also be isolated from tissues other than brain such as spinal cord, retina, myenteric plexus or the electric ray electric organ.[7][8] Synaptosomes may be used to isolate postsynaptic densities[9] or the presynaptic active zone with attached synaptic vesicles.[10] Accordingly, various subproteomes of isolated synaptosomes, such as synaptic vesicles, synaptic membranes, or postsynaptic densities can now be studied by proteomic techniques, leading to a deeper understanding of the molecular machinery of brain neurotransmission and neuroplasticity.[11][12][13][14]
References
- ^ Hebb CO, Whittaker VP (1958) Intracellular distributions of acetylcholine and choline acetylase. J Physiol 142:187-96.
- ^ Gray EG, Whittaker VP (1960). The isolation of synaptic vesicles from the central nervous system. J Physiol (London) 153: 35P-37P.
- ^ Gray EG, Whittaker VP (1962) The isolation of nerve endings from brain: an electron-microscopic study of cell fragments derived by homogenization and centrifugation. J Anat 96: 79-88.
- ^ Whittaker VP, Michaelson IA, Kirkland RJ (1964) The separation of synaptic vesicles from nerve-ending particles ('synaptosomes'). Biochem J 90:293-303.
- ^ Whittaker VP (1965) The application of subcellular fractionation techniques to the study of brain function. Progr Biophys Mol Biol 15, 38-96.
- ^ Ivannikov, M.; et al. (2013). "Synaptic vesicle exocytosis in hippocampal synaptosomes correlates directly with total mitochondrial volume". J. Mol. Neurosci. 49 (1): 223–230. doi:10.1007/s12031-012-9848-8. PMID 22772899.
- ^ Whittaker VP (1993) Thirty years of synaptosome research. J Neurocytol 22: 735-742.
- ^ Breukel AI, Besselsen E, Ghijsen WE (1997) Synaptosomes. A model system to study release of multiple classes of neurotransmitters. Methods Mol Biol 72:33-47.
- ^ Carlin RK, Grab DJ, Cohen RS, Siekevitz P (1980) Isolation and characterization of postsynaptic densities from various brain regions: enrichment of different types of postsynaptic densities. J Cell Biol 86:831-845.
- ^ Morciano M, Burré J, Corvey C, Karas M, Zimmermann H, Volknandt W (2005) Immunoisolation of two synaptic vesicle pools from synaptosomes: a proteomics analysis. J Neurochem 95:1732-1745.
- ^ Bai F, Witzmann FA (2007) Synaptosome Proteomics. Subcell Biochem 43:77–98.
- ^ Morciano M, Burré J, Corvey C, Karas M, Zimmermann H, Volknandt W (2005) Immunoisolation of two synaptic vesicle pools from synaptosomes: a proteomics analysis. J Neurochem 95:1732-1745.
- ^ Burré J, Beckhaus T, Schägger H, Corvey C, Hofmann S, Karas M, Zimmermann H, Volknandt W (2006) Analysis of the synaptic vesicle proteome using three gel-based protein separation techniques. Proteomics 6:6250-6262.
- ^ Takamori S, Holt M, Stenius K, Lemke EA, Grønborg M, Riedel D, Urlaub H, Schenck S, Brügger B, Ringler P, Müller SA, Rammner B, Gräter F, Hub JS, De Groot BL, Mieskes G, Moriyama Y, Klingauf J, Grubmüller H, Heuser J, Wieland F, Jahn R (2006) Molecular anatomy of a trafficking organelle. Cell 127:831-846.
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- The new psychoactive substances 5-(2-aminopropyl)indole (5-IT) and 6-(2-aminopropyl)indole (6-IT) interact with monoamine transporters in brain tissue.
- Marusich JA1, Antonazzo KR2, Blough BE2, Brandt SD3, Kavanagh PV4, Partilla JS5, Baumann MH5.
- Neuropharmacology.Neuropharmacology.2016 Feb;101:68-75. doi: 10.1016/j.neuropharm.2015.09.004. Epub 2015 Sep 8.
- In recent years, use of psychoactive synthetic stimulants has grown rapidly. 5-(2-Aminopropyl)indole (5-IT) is a synthetic drug associated with a number of fatalities, that appears to be one of the newest 3,4-methylenedioxymethamphetamine (MDMA) replacements. Here, the monoamine-releasing properties
- PMID 26362361
- Dietary obesity reversibly induces synaptic stripping by microglia and impairs hippocampal plasticity.
- Hao S1, Dey A1, Yu X1, Stranahan AM2.
- Brain, behavior, and immunity.Brain Behav Immun.2016 Jan;51:230-9. doi: 10.1016/j.bbi.2015.08.023. Epub 2015 Aug 31.
- Obesity increases risk of age-related cognitive decline and is accompanied by peripheral inflammation. Studies in rodent models of obesity have demonstrated that impaired hippocampal function correlates with microglial activation, but the possibility that neuron/microglia interactions might be pertu
- PMID 26336035
- Abuse-Related Neurochemical Effects of Para-Substituted Methcathinone Analogs in Rats: Microdialysis Studies of Nucleus Accumbens Dopamine and Serotonin.
- Suyama JA1, Sakloth F1, Kolanos R1, Glennon RA1, Lazenka MF1, Negus SS1, Banks ML2.
- The Journal of pharmacology and experimental therapeutics.J Pharmacol Exp Ther.2016 Jan;356(1):182-90. doi: 10.1124/jpet.115.229559. Epub 2015 Oct 15.
- Methcathinone (MCAT) is a monoamine releaser and parent compound to a new class of designer drugs that includes the synthetic cathinones mephedrone and flephedrone. Using MCAT and a series of para-substituted (or 4-substituted) MCAT analogs, it has been previously shown that expression of abuse-rela
- PMID 26645638
Japanese Journal
- Dopamine Release Suppression Dependent on an Increase of Intracellular Ca²⁺ Contributed to Rotenone-induced Neurotoxicity in PC12 Cells
- Regeneration-dependent conditional gene knockdown (Readyknock) in planarian: demonstration of requirement for Djsnap-25 expression in the brain for negative phototactic behavior
- Transcriptome analysis reveals the population of dendritic RNAs and their redistribution by neural activity
- Neuroscience research : the official journal of the Japan Neuroscience Society 57(3), 411-423, 2007-03-01
- NAID 10024413353
Related Links
- A synaptosome is an isolated synaptic terminal from a neuron. Synaptosomes are obtained after homogenization and fractionation of nervous tissue. The fractionation step involves several rounds of centrifugation to separate various ...
Related Pictures
★リンクテーブル★
[★]
- 関
- synaptosome
[★]
- 英
- synaptosome、synaptosomal