Literature DB >> 9001700

Rapid conversion of myelin-associated glycoprotein to a soluble derivative in primates.

J R Möller1.   

Abstract

Myelin-associated glycoprotein (MAG) is susceptible to proteolysis by a calcium-activated neutral protease which is located in myelin. The conversion of MAG (M(r) 100,000) to its soluble derivative dMAG (M(r) 90,000) occurs much more rapidly in myelin from human white matter than in myelin from rat brain, and the rate of formation of dMAG is increased even more in myelin from white matter of patients with multiple sclerosis (MS). The MAG to dMAG conversion was studied in several species, ranging from mice to non-human primates and humans to determine what animal model would be the most appropriate for investigating the MAG to dMAG reaction in demyelinating disorders. Myelin fractions from brains of these species were prepared and incubated at 37 degrees C in 0.2 M NH4HCO3, pH 7.4 for time periods ranging from 5 min to 24 h. Western blot analysis of the samples, taken at the end points of the different incubation periods, showed that the time required for a 50% conversion of MAG to dMAG was 18-24 h in myelin from rodents to bovine. The non-human primate studies revealed a 50% conversion at 2 h for marmoset samples and rhesus monkey samples, 20 min for gorilla samples and 10 min for chimpanzee samples. Human myelin samples needed only 5 min for a 50% conversion of MAG to dMAG. The reason for the significantly faster formation of dMAG in primate myelin is unknown and currently is being investigated.

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Year:  1996        PMID: 9001700     DOI: 10.1016/s0006-8993(96)00882-7

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  4 in total

Review 1.  Mechanism of myelin breakdown in experimental demyelination: a putative role for calpain.

Authors:  K E Schaecher; D C Shields; N L Banik
Journal:  Neurochem Res       Date:  2001-06       Impact factor: 3.996

2.  Characterization of myelin-associated glycoprotein (MAG) proteolysis in the human central nervous system.

Authors:  J W Stebbins; H Jaffe; J R Möller
Journal:  Neurochem Res       Date:  1998-07       Impact factor: 3.996

Review 3.  Possible Influences of Endogenous and Exogenous Ligands on the Evolution of Human Siglecs.

Authors:  Takashi Angata
Journal:  Front Immunol       Date:  2018-12-04       Impact factor: 7.561

4.  Axon-Myelin Unit Blistering as Early Event in MS Normal Appearing White Matter.

Authors:  Antonio Luchicchi; Bert't Hart; Irene Frigerio; Anne-Marie van Dam; Laura Perna; Herman L Offerhaus; Peter K Stys; Geert J Schenk; Jeroen J G Geurts
Journal:  Ann Neurol       Date:  2021-01-27       Impact factor: 10.422

  4 in total

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