» Articles » PMID: 20224973

Derivation, Culture, and Characterization of VUB HESC Lines

Overview
Publisher Springer
Specialties Biology
Cell Biology
Date 2010 Mar 13
PMID 20224973
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

In this report, we present the derivation and characterization of 15 hESC lines established at the Vrije Universiteit Brussel, Belgium in collaboration with the Universitair Ziekenhuis Brussel, Belgium, using surplus in vitro fertilization embryos and embryos carrying monogenic disorders donated for research. Four lines were derived from blastocyst-stage embryos presumed to be genetically normal, and 11 hESC lines were obtained from embryos shown to carry genetic mutations by preimplantation genetic diagnosis. All the lines express markers of pluripotency as determined by immunocytochemistry and RT-PCR, and formed teratomas when injected into SCID mice. All VUB hESC lines, except for VUB17, are reported in the European hESC registry and are available upon request after signing a Material Transfer Agreement from the VUB (contact person: Prof. Dr. Karen Sermon; Karen.Sermon@uzbrussel.be).

Citing Articles

Human stem cell models for Marfan syndrome: a .

Aalders J, Mosquera L, van Hengel J Front Cell Dev Biol. 2025; 12():1498669.

PMID: 39830211 PMC: 11739147. DOI: 10.3389/fcell.2024.1498669.


Gain of 1q confers an MDM4-driven growth advantage to undifferentiated and differentiating hESC while altering their differentiation capacity.

Krivec N, Couvreu de Deckersberg E, Lei Y, Al Delbany D, Regin M, Verhulst S Cell Death Dis. 2024; 15(11):852.

PMID: 39572522 PMC: 11582570. DOI: 10.1038/s41419-024-07236-x.


De Novo Cancer Mutations Frequently Associate with Recurrent Chromosomal Abnormalities during Long-Term Human Pluripotent Stem Cell Culture.

Al Delbany D, Ghosh M, Krivec N, Huyghebaert A, Regin M, Duong M Cells. 2024; 13(16).

PMID: 39195283 PMC: 11353044. DOI: 10.3390/cells13161395.


SALL3 mediates the loss of neuroectodermal differentiation potential in human embryonic stem cells with chromosome 18q loss.

Lei Y, Al Delbany D, Krivec N, Regin M, Couvreu de Deckersberg E, Janssens C Stem Cell Reports. 2024; 19(4):562-578.

PMID: 38552632 PMC: 11096619. DOI: 10.1016/j.stemcr.2024.03.001.


Uncovering low-level mosaicism in human embryonic stem cells using high throughput single cell shallow sequencing.

Keller A, Tilleman L, Dziedzicka D, Zambelli F, Sermon K, Van Nieuwerburgh F Sci Rep. 2019; 9(1):14844.

PMID: 31619727 PMC: 6796059. DOI: 10.1038/s41598-019-51314-6.


References
1.
Sermon K, Van Steirteghem A, Liebaers I . Preimplantation genetic diagnosis. Lancet. 2004; 363(9421):1633-41. DOI: 10.1016/S0140-6736(04)16209-0. View

2.
Spits C, Mateizel I, Geens M, Mertzanidou A, Staessen C, Vandeskelde Y . Recurrent chromosomal abnormalities in human embryonic stem cells. Nat Biotechnol. 2008; 26(12):1361-3. DOI: 10.1038/nbt.1510. View

3.
De Temmerman N, Seneca S, VAN Steirteghem A, Haentjens P, Van der Elst J, Liebaers I . CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation. Mol Hum Reprod. 2008; 14(7):405-12. DOI: 10.1093/molehr/gan034. View

4.
Abeliovich A, Doege C . Reprogramming therapeutics: iPS cell prospects for neurodegenerative disease. Neuron. 2009; 61(3):337-9. PMC: 3659427. DOI: 10.1016/j.neuron.2009.01.024. View

5.
Thomson J, Itskovitz-Eldor J, Shapiro S, Waknitz M, Swiergiel J, Marshall V . Embryonic stem cell lines derived from human blastocysts. Science. 1998; 282(5391):1145-7. DOI: 10.1126/science.282.5391.1145. View