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GM04934 Fibroblast

Description:

ADRENOLEUKODYSTROPHY; ALD

Affected:

Yes

Sex:

Male

Age:

7 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Class Disorders of Steroid Metabolism
Cell Type Fibroblast
Transformant Untransformed
Race White
Relation to Proband proband
Confirmation Biochemical characterization after cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Elevated C26:C22 fatty acid ratio in fibroblasts and plasma

Characterizations

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PDL at Freeze 4.94
Passage Frozen 7
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 

Phenotypic Data

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Remarks Elevated C26:C22 fatty acid ratio in fibroblasts and plasma

Publications

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Monternier PA, Singh J, Parasar P, Theurey P, DeWitt S, Jacques V, Klett E, Kaur N, Nagaraja TN, Moller DE, Hallakou-Bozec S, Therapeutic potential of deuterium-stabilized (R)-pioglitazone-PXL065-for X-linked adrenoleukodystrophy Journal of inherited metabolic disease: 2022
PubMed ID: 35510808
 
Lee DK, Long NP, Jung J, Kim TJ, Na E, Kang YP, Kwon SW, Jang J, Integrative lipidomic and transcriptomic analysis of X-linked adrenoleukodystrophy reveals distinct lipidome signatures between adrenomyeloneuropathy and childhood cerebral adrenoleukodystrophy Biochemical and biophysical research communications: 2018
PubMed ID: 30509496
 
Singh J, Khan M, Singh I, Caffeic acid phenethyl ester induces adrenoleukodystrophy (Abcd2) gene in human X-ALD fibroblasts and inhibits the proinflammatory response in Abcd1/2 silenced mouse primary astrocytes Biochimica et biophysica acta: 2012
PubMed ID: 23318275
 
Pahan K, Khan M, Singh I, Therapy for X-adrenoleukodystrophy: normalization of very long chain fatty acids and inhibition of induction of cytokines by cAMP. J Lipid Res39(5):1091-100 1998
PubMed ID: 9610777
 
Sandhir R, Khan M, Chahal A, Singh I, Localization of nervonic acid beta-oxidation in human and rodent peroxisomes: impaired oxidation in Zellweger syndrome and X-linked adrenoleukodystrophy. J Lipid Res39:2161-71 1998
PubMed ID: 9799802
 
Wilson R, Tocher DR, Sargent JR, Effects of exogenous monounsaturated fatty acids on fatty acid metabolism in cultured skin fibroblasts from adrenoleukodystrophy patients. J Neurol Sci109:207-14 1992
PubMed ID: 1634904

External Links

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dbSNP dbSNP ID: 21713
Gene Cards ALD
NCBI GTR 300100 ADRENOLEUKODYSTROPHY; ALD
OMIM 300100 ADRENOLEUKODYSTROPHY; ALD
Omim Description ADDISON DISEASE AND CEREBRAL SCLEROSIS
  ADRENOLEUKODYSTROPHY; ALD
  ADRENOMYELONEUROPATHY; AMN
  BRONZE SCHILDER'S DISEASE
  MELANODERMIC LEUKODYSTROPHYADRENOLEUKODYSTROPHY PROTEIN, INCLUDED; ALDP, INCLUDED
  SIEMERLING-CREUTZFELDT DISEASE

Culture Protocols

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Passage Frozen 7
Split Ratio 1:5
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not inactivated
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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