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GM03040 Fibroblast

Description:

HYPERCHOLESTEROLEMIA, FAMILIAL; FHC
LOW DENSITY LIPOPROTEIN RECEPTOR; LDLR

Affected:

Yes

Sex:

Male

Age:

9 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 Lipid Metabolism
Cell Type Fibroblast
Tissue Type Skin
Transformant Untransformed
Race White
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected; very high serum LDL (820 mg/L), triglycerides: 85; normal triglycerides; cutaneous and tendinous xanthomas; corneal arcus; no response to diet and bile chelating resins; fibroblast assays show minimal binding, internalization and degradation and oleate incorporation into cholesterol ester; 120I-LDL binding assay showed this line to have <5% normal activity (LDL receptor negative); Family history: mother’s side of the family reported to be strongly positive for early onset atherosclerosis and hypercholesterolemia; affected mother(GM03065)-serum cholesterol level 870 mg/L, triglycerides: 51, no xanthomas, no clinical evidence of atherosceloris; affected father(GM03064)-serum cholesterol level 299 mg/L, triglycerides: 150, no xanthomas, no clinical evidence of atherosclerosis.

Characterizations

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Passage Frozen 16
 
IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis
 
Gene LDLR
Chromosomal Location 19p13.2-p13.1
Allelic Variant 1 606945.0005; HYPERCHOLESTEROLEMIA, FAMILIAL
Identified Mutation GLY197DEL
 
Gene LDLR
Chromosomal Location 19p13.2-p13.1
Allelic Variant 2 606945.0005; HYPERCHOLESTEROLEMIA, FAMILIAL
Identified Mutation GLY197DEL

Phenotypic Data

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Remarks Clinically affected; very high serum LDL (820 mg/L), triglycerides: 85; normal triglycerides; cutaneous and tendinous xanthomas; corneal arcus; no response to diet and bile chelating resins; fibroblast assays show minimal binding, internalization and degradation and oleate incorporation into cholesterol ester; 120I-LDL binding assay showed this line to have <5% normal activity (LDL receptor negative); Family history: mother’s side of the family reported to be strongly positive for early onset atherosclerosis and hypercholesterolemia; affected mother(GM03065)-serum cholesterol level 870 mg/L, triglycerides: 51, no xanthomas, no clinical evidence of atherosceloris; affected father(GM03064)-serum cholesterol level 299 mg/L, triglycerides: 150, no xanthomas, no clinical evidence of atherosclerosis.

Publications

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Omer L, Hindi L, Militello G, Stivers KB, Tien KC, Boyd NL, Familial hypercholesterolemia class II low density lipoprotein-receptor response to statin treatment Disease models & mechanisms: 2019
PubMed ID: 32005714
 
Villard EF, Thedrez A, Blankenstein J, Croyal M, Tran TT, Poirier B, Le Bail JC, Illiano S, Nobécourt E, Krempf M, Blom DJ, Marais AD, Janiak P, Muslin AJ, Guillot E, Lambert G, PCSK9 Modulates the Secretion But Not the Cellular Uptake of Lipoprotein(a) Ex Vivo: An Effect Blunted by Alirocumab JACC Basic to translational science1:419-427 2018
PubMed ID: 29308438
 
Agnello V, Abel G, Elfahal M, Knight GB, Zhang QX, Hepatitis C virus and other flaviviridae viruses enter cells via low density lipoprotein receptor. Proc Natl Acad Sci U S A96:12766-71 1999
PubMed ID: 10535997
 
Chatterjee, Alterations in cell surface glycosphingolipids and their metabolism in familial hypercholesterolemic fibroblasts. (from CELL SURFACE GLYCOLIPIDS, C.C. Sweeley, ed.) ACS Symposium Series16:265 (1980):12766-71 1980
PubMed ID: 10535997

External Links

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dbSNP dbSNP ID: 21124
Gene Cards LDLR
Gene Ontology GO:0004888 transmembrane receptor activity
GO:0005041 low-density lipoprotein receptor activity
GO:0005319 lipid transporter activity
GO:0005509 calcium ion binding
GO:0005887 integral to plasma membrane
GO:0005905 coated pit
GO:0006493 O-linked glycosylation
GO:0006629 lipid metabolism
GO:0006869 lipid transport
GO:0006897 endocytosis
GO:0008034 lipoprotein binding
GO:0008203 cholesterol metabolism
NCBI Gene Gene ID:3949
NCBI GTR 143890 HYPERCHOLESTEROLEMIA, FAMILIAL, 1; FHCL1
606945 LOW DENSITY LIPOPROTEIN RECEPTOR; LDLR
OMIM 143890 HYPERCHOLESTEROLEMIA, FAMILIAL, 1; FHCL1
606945 LOW DENSITY LIPOPROTEIN RECEPTOR; LDLR
Omim Description FH
  HYPERCHOLESTEROLEMIA, FAMILIAL; FHC
  HYPERLIPOPROTEINEMIA, TYPE IIA
  LDL RECEPTOR DISORDERLOW DENSITY LIPOPROTEIN RECEPTOR, INCLUDED; LDLR, INCLUDED

Culture Protocols

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Passage Frozen 16
Split Ratio 1:3
Temperature 37 C
Percent CO2 5%
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
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
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$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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