Setting up a Facility for Human Embryonic Stem Cell Research

Publisher Summary Scientists have distilled their collective experience of setting up over ten stem cell laboratories on three continents, with the intention of lessening the pain of others who are setting up such laboratories for the first time. They are sure of two things: first, the effort extended in setting up systems and processes for a laboratory will be repaid many fold in future efficiencies; and second, the effort to set systems in place from the very beginning is much less than retro-fitting them. Therefore, if someone set up a laboratory from the scratch, the advice is to try to get it right from the beginning. The critical issue of setting up the laboratory is planning for long-term success. This will rest on the functional design and utilization of the space and the appropriate equipment. Most important is the implementation of quality control systems that allow a continuous supply of validated cells and reagents. The chapter provides most of the protocols and methods for these systems, and other resources are also available; however, wherever possible, it is recommneded that key personnel should receive specific training in human embryonic stem cell (hESC) manipulation, and that the laboratory develop a network of communication and collaboration with other hESC group.

[1]  J A Thomson,et al.  Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture. , 2000, Developmental biology.

[2]  J. Thomson,et al.  Derivation of human embryonic stem cells in defined conditions , 2006, Nature Biotechnology.

[3]  Takumi Miura,et al.  Properties of four human embryonic stem cell lines maintained in a feeder‐free culture system , 2004, Developmental dynamics : an official publication of the American Association of Anatomists.

[4]  Takumi Miura,et al.  Monitoring early differentiation events in human embryonic stem cells by massively parallel signature sequencing and expressed sequence tag scan. , 2004, Stem cells and development.

[5]  A. Chakravarti,et al.  Genomic alterations in cultured human embryonic stem cells , 2005, Nature Genetics.

[6]  Ying Liu,et al.  Assessing Self‐Renewal and Differentiation in Human Embryonic Stem Cell Lines , 2006, Stem cells.

[7]  J. Thomson,et al.  Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells , 2004, Nature Biotechnology.

[8]  K. Sidhu,et al.  Derivation of three clones from human embryonic stem cell lines by FACS sorting and their characterization. , 2006, Stem cells and development.

[9]  A. Pyle,et al.  Neurotrophins mediate human embryonic stem cell survival , 2006, Nature Biotechnology.

[10]  J. Stringer,et al.  Embryonic stem cells and somatic cells differ in mutation frequency and type , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[11]  M. Kubista,et al.  Monitoring Differentiation of Human Embryonic Stem Cells Using Real‐Time PCR , 2005, Stem cells.

[12]  Takumi Miura,et al.  Long‐term culture of human embryonic stem cells in feeder‐free conditions , 2004, Developmental dynamics : an official publication of the American Association of Anatomists.

[13]  R. Puri,et al.  Gene expression in human embryonic stem cell lines: unique molecular signature. , 2004, Blood.

[14]  I. Khrebtukova,et al.  MPSS profiling of human embryonic stem cells , 2004, BMC Developmental Biology.

[15]  R. Pedersen,et al.  Epigenetic status of human embryonic stem cells , 2005, Nature Genetics.

[16]  J. Crook,et al.  Karyotype of human ES cells during extended culture , 2004, Nature Biotechnology.