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GM18455 Fibroblast

Description:

NIEMANN-PICK DISEASE, TYPE C2
NPC2 GENE; NPC2

Affected:

Yes

Sex:

Male

Age:

No Data

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

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Lysosomal Storage Diseases
Class Disorders of Lipid Metabolism
Cell Type Fibroblast
Transformant Untransformed
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Clinically affected; the donor subject is a compound heterozygote at the NPC2 gene locus: allele 1 carries a substitution (G>T) at nucleotide 58 (c.58G>T) in exon 1, resulting in a nonsense mutation at codon 20 [E20X (GLU20TER)]; allele 2 carries a substitution (G>T) at nucleotide 140 (c.140G>T) in exon 2, resulting in a missense mutation at codon 47 [C47F (CYS47PHE)]; the first nucleotide of the initiating MET codon is numbered +1; fibroblasts showed no detectable activity in a cholesterol esterification assay; a complementation test showed that the cells were type 2 [see Park et al. Hum Mut 22:313-325 (2003)]. This fibroblast is a characteristically poor grower and will only be shipped frozen; requires particular care during growth; the recommended seeding density is 15,000 to 20,000 cells per cm2.

Characterizations

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PDL at Freeze 6.51
Passage Frozen 3
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase,Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 
Gene NPC2
Chromosomal Location 14q24.3
Allelic Variant 1 601015.0001; NIEMANN-PICK DISEASE, TYPE C2
Identified Mutation GLU20TER
 
Gene NPC2
Chromosomal Location 14q24.3
Allelic Variant 2 C47F; NIEMANN-PICK DISEASE, TYPE C2
Identified Mutation CYS47PHE

Phenotypic Data

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Remarks Clinically affected; the donor subject is a compound heterozygote at the NPC2 gene locus: allele 1 carries a substitution (G>T) at nucleotide 58 (c.58G>T) in exon 1, resulting in a nonsense mutation at codon 20 [E20X (GLU20TER)]; allele 2 carries a substitution (G>T) at nucleotide 140 (c.140G>T) in exon 2, resulting in a missense mutation at codon 47 [C47F (CYS47PHE)]; the first nucleotide of the initiating MET codon is numbered +1; fibroblasts showed no detectable activity in a cholesterol esterification assay; a complementation test showed that the cells were type 2 [see Park et al. Hum Mut 22:313-325 (2003)]. This fibroblast is a characteristically poor grower and will only be shipped frozen; requires particular care during growth; the recommended seeding density is 15,000 to 20,000 cells per cm2.

Publications

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Liedtke M, Völkner C, Hermann A, Frech MJ, Impact of Organelle Transport Deficits on Mitophagy and Autophagy in Niemann-Pick Disease Type C Cells11: 2022
PubMed ID: 35159316
 
Juhl AD, Heegaard CW, Werner S, Schneider G, Krishnan K, Covey DF, Wüstner D, Quantitative imaging of membrane contact sites for sterol transfer between endo-lysosomes and mitochondria in living cells Scientific reports11:8927 2020
PubMed ID: 33903617
 
Juhl AD, Lund FW, Jensen MLV, Szomek M, Heegaard CW, Guttmann P, Werner S, McNally J, Schneider G, Kapishnikov S, Wüstner D, Niemann Pick C2 protein enables cholesterol transfer from endo-lysosomes to the plasma membrane for efflux by shedding of extracellular vesicles Chemistry and physics of lipids235:105047 2020
PubMed ID: 33422548
 
Liu EA, Schultz ML, Mochida C, Chung C, Paulson HL, Lieberman AP, Fbxo2 mediates clearance of damaged lysosomes and modifies neurodegeneration in the Niemann-Pick C brain JCI insight235:105047 2020
PubMed ID: 32931479
 
McCauliff LA, Langan A, Li R, Ilnytska O, Bose D, Waghalter M, Lai K, Kahn PC, Storch J, Intracellular cholesterol trafficking is dependent upon NPC2 interaction with Lysobisphosphatidic Acid eLife8:105047 2019
PubMed ID: 31580258
 
Petersen D, Reinholdt P, Szomek M, Hansen SK, Poongavanam V, Dupont A, Heegaard CW, Krishnan K, Fujiwara H, Covey DF, Ory DS, Kongsted J, Wüstner D, Binding and intracellular transport of 25-hydroxycholesterol by Niemann-Pick C2 protein Biochimica et biophysica acta Biomembranes8:183063 2019
PubMed ID: 31521631
 
Völkner C, Peter F, Liedtke M, Krohn S, Lindner I, Murua Escobar H, Cimmaruta C, Lukas J, Hermann A, Frech MJ, Generation of the Niemann-Pick type C2 patient-derived iPSC line AKOSi001-A Stem cell research41:101606 2019
PubMed ID: 31669975
 
Berzina Z, Solanko LM, Mehadi AS, Jensen MLV, Lund FW, Modzel M, Szomek M, Solanko KA, Dupont A, Nielsen GK, Heegaard CW, Ejsing CS, Wüstner D, Niemann-Pick C2 protein regulates sterol transport between plasma membrane and late endosomes in human fibroblasts Chemistry and physics of lipids213:48-61 2018
PubMed ID: 29580834
 
Höglinger D, Burgoyne T, Sanchez-Heras E, Hartwig P, Colaco A, Newton J, Futter CE, Spiegel S, Platt FM, Eden ER, NPC1 regulates ER contacts with endocytic organelles to mediate cholesterol egress Nature communications10:4276 2017
PubMed ID: 31537798
 
Modzel M, Solanko KA, Szomek M, Hansen SK, Dupont A, Nåbo LJ, Kongsted J, Wüstner D, Live-cell imaging of new polyene sterols for improved analysis of intracellular cholesterol transport Journal of microscopy10:4276 2017
PubMed ID: 29516493
 
Wang ML, Motamed M, Infante RE, Abi-Mosleh L, Kwon HJ, Brown MS, Goldstein JL, Identification of surface residues on Niemann-Pick C2 essential for hydrophobic handoff of cholesterol to NPC1 in lysosomes Cell metabolism12:166-73 2010
PubMed ID: 20674861

External Links

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Gene Cards NPC2
NCBI Gene Gene ID:10577
NCBI GTR 601015 NPC INTRACELLULAR CHOLESTEROL TRANSPORTER 2; NPC2
607625 NIEMANN-PICK DISEASE, TYPE C2; NPC2
OMIM 601015 NPC INTRACELLULAR CHOLESTEROL TRANSPORTER 2; NPC2
607625 NIEMANN-PICK DISEASE, TYPE C2; NPC2
Omim Description NIEMANN-PICK DISEASE, TYPE C2

Culture Protocols

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Cumulative PDL at Freeze 6.51
Passage Frozen 3
Split Ratio 1:2
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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