Saposins A, B, C, and D in plasma of patients with lysosomal storage disorders.
نویسندگان
چکیده
BACKGROUND Early diagnosis of lysosomal storage disorders (LSDs), before the onset of irreversible pathology, will be critical for maximum efficacy of many current and proposed therapies. To search for potential markers of LSDs, we measured saposins A, B, C, and D in patients with these disorders. METHODS Four time-delayed fluorescence immunoquantification assays were used to measure each of the saposins in plasma from 111 unaffected individuals and 334 LSD-affected individuals, representing 28 different disorders. RESULTS Saposin A was increased above the 95th centile of the control population in 59% of LSD patients; saposins B, C, and D were increased in 25%, 61%, and 57%, respectively. Saposins were increased in patients from several LSD groups that in previous studies did not show an increase of lysosome-associated membrane protein-1 (LAMP-1). CONCLUSION Saposins may be useful markers for LSDs when used in conjunction with LAMP-1.
منابع مشابه
Saposins: structure, function, distribution, and molecular genetics.
Saposins A, B, C, and D are small heat-stable glycoproteins derived from a common precursor protein, prosaposin. These mature saposins, as well as prosaposin, activate several lysosomal hydrolases involved in the metabolism of various sphingolipids. All four saposins are structurally similar to one another including placement of six cysteines, a glycosylation site, and conserved prolines in ide...
متن کاملDistribution of saposin proteins (sphingolipid activator proteins) in lysosomal storage and other diseases.
Saposins (A, B, C, and D) are small glycoproteins required for the hydrolysis of sphingolipids by specific lysosomal hydrolases. Concentrations of these saposins in brain, liver, and spleen from normal humans as well as patients with lysosomal storage disease were determined. A quantitative HPLC method was used for saposin A, C, and D and a stimulation assay was used for saposin B. In normal ti...
متن کاملCombined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and alpha-hydroxy ceramide accumulation, and altered prosaposin trafficking.
Saposins (A, B, C and D) are approximately 80 amino acid stimulators of glycosphingolipid (GSL) hydrolases that derive from a single precursor, prosaposin. In both humans and mice, prosaposin/saposin deficiencies lead to severe neurological deficits. The CD-/- mice with saposin C and D combined deficiencies were produced by introducing genomic point mutations into a critical cysteine in each of...
متن کاملRole of saposin C and D in auditory and vestibular function.
OBJECTIVES/HYPOTHESIS Saposins are small proteins derived from a precursor protein, prosaposin. Each of the four saposins (A-D) is necessary for the activity of lysosomal glycosphingolipid hydrolases. Individual saposin mutations lead to lysosomal storage diseases, some of which are associated with hearing loss. Here we evaluate the effects of the loss of saposins C and D on auditory and vestib...
متن کاملProsaposin Precursor Protein: Functions and Medical Applications. Review
Prosaposin is a precursor of four saposins, termed saposin A, B, C, and D, which activate glycosphingolipid hydrolysis. Inherited deficiency of saposins leads to several forms of lysosomal storage disease. Besides the lysosomal function, a secreted form of prosaposin displays several other properties. This precursor was shown in rodents to maintain the nervous system associated with oxidative s...
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ورودعنوان ژورنال:
- Clinical chemistry
دوره 46 2 شماره
صفحات -
تاریخ انتشار 2000