scholarly journals A culture system using human foreskin fibroblasts as feeder cells allows production of human embryonic stem cells

2003 ◽  
Vol 18 (7) ◽  
pp. 1404-1409 ◽  
Author(s):  
O. Hovatta
Keyword(s):  
Stem Cells ◽  
Embryonic Stem Cells ◽  
Human Embryonic Stem Cells ◽  
Culture System ◽  
Embryonic Stem ◽  
Feeder Cells ◽  
Human Foreskin Fibroblasts

FGF2 secreting human fibroblast feeder cells: A novel culture system for human embryonic stem cells

2008 ◽  
Vol 75 (10) ◽  
pp. 1523-1532 ◽  
Author(s):  
Shobhit Saxena ◽  
Madhuri Hanwate ◽  
Kaushik Deb ◽  
Vijay Sharma ◽  
Satish Totey
Keyword(s):  
Stem Cells ◽  
Embryonic Stem Cells ◽  
Human Embryonic Stem Cells ◽  
Human Fibroblast ◽  
Culture System ◽  
Embryonic Stem ◽  
Feeder Cells

Human embryonic stem cells derived without feeder cells

The Lancet ◽  
2005 ◽  
Vol 365 (9471) ◽  
pp. 1636-1641 ◽  
Author(s):  
Irina Klimanskaya ◽  
Young Chung ◽  
Lorraine Meisner ◽  
Julie Johnson ◽  
Michael D West ◽  
...  
Keyword(s):  
Stem Cells ◽  
Embryonic Stem Cells ◽  
Human Embryonic Stem Cells ◽  
Embryonic Stem ◽  
Feeder Cells

Comparative study of mouse and human feeder cells for human embryonic stem cells

2008 ◽  
Vol 52 (4) ◽  
pp. 353-363 ◽  
Author(s):  
Livia Eiselleova ◽  
Iveta Peterkova ◽  
Jakub Neradil ◽  
Iva Slaninova ◽  
Ales Hampl ◽  
...  
Keyword(s):  
Stem Cells ◽  
Embryonic Stem Cells ◽  
Comparative Study ◽  
Human Embryonic Stem Cells ◽  
Embryonic Stem ◽  
Feeder Cells

P–797 A novel method for establishing human embryonic stem cells independent of feeder cells

2021 ◽  
Vol 36 (Supplement_1) ◽  
Author(s):  
B Cai
Keyword(s):  
Stem Cells ◽  
Stem Cell ◽  
Embryonic Stem Cells ◽  
Embryonic Stem Cell ◽  
Success Rate ◽  
Cell Lines ◽  
Human Embryonic Stem Cells ◽  
Embryonic Stem ◽  
Feeder Cells ◽  
Novel Method

Abstract Study question Is there a efficient establishing method of human embryonic stem cells directly from the human blastocysts independent of feeder cells? Summary answer We established a novel method of generating human embryonic stem cells directly from human blastocysts independent of feeder layer cells. What is known already Establishing embryonic stem cells lines mainly needed to coculture ICM clumps with feeder cells (like mouse or human fibroblasts) ,this brought in potential heterogeneous pollution.Although there had be some reports about generating human ESCs independent of feeder cells,but the efficiency was low and conditioned medium were unstable and also had the biological contamination. Study design, size, duration We used ten day5/6 donated human blastocysts from our reproductive center ,most of them were genetically diseased embryos with abnormal PGT diagnosis.After establishing ESCs procedure , all the cell lines were identified with pluripotency and differentiation potential tests.The success rate of system was calculated and compared with the conventional methods. Participants/materials, setting, methods In brief, ICM clumps were separated mechanically by using a micromanipulation system,and then transferred to a 30ul mTESR plus culture media drop pretreated with the geltrex (1:100 dilution) matrix and oxygen concentration was 5%. When cells attached and migrated,we also used laser to destroy the remaining trophoblast cells.About 10 days,the typical ES clone can be mechanically passaged and cells can be cultured in normal oxygen concentrations after passage 2. . Main results and the role of chance Using this method we had successfully established nine embryonic stem cell lines from donated human blastocysts ,the success rate was 90% (9/10). Each cell lines had passed the evaluation test of embryonic stem cell. When compared with the conventional feeder cells dependent method,our novol methods not only eliminated the pollution from heterogeneous cells,but also had higher success rate (90% vs 25%). Limitations, reasons for caution Due to the scarcity of donated human blastocysts, this experiment was a single-center experiment with small samples. Wider implications of the findings: We speculated that the batch differences of culture dishes, matrix and culture medium might affect the establish efficiency , and how to carry out a high level of quality control work might be the key factor to keep the system stable. Trial registration number basic research

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