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Open AccessHighly AccessMethodology

Laser-assisted blastocyst dissection and subsequent cultivation of embryonic stem cells in a serum/cell free culture system: applications and preliminary results in a murine model

Noriko Tanaka1 email, Takumi Takeuchi1 email, Queenie V Neri1 email, Eric Scott Sills2 email and Gianpiero D Palermo1 email

Center for Reproductive Medicine and Infertility, Weill Medical College of Cornell University, New York, NY 10021, USA

Department of Obstetrics, Gynecology and Reproductive Research, Murphy Medical Center, Murphy, NC, USA

author email corresponding author email

Journal of Translational Medicine 2006, 4:20doi:10.1186/1479-5876-4-20

Published: 8 May 2006

Abstract

Background

To evaluate embryonic stem cell (ESC) harvesting methods with an emphasis on derivation of ESC lines without feeder cells or sera. Using a murine model, laser-assisted blastocyst dissection was performed and compared to conventional immunosurgery to assess a novel laser application for inner cell mass (ICM) isolation.

Methods

Intact blastocysts or isolated ICMs generated in a standard mouse strain were plated in medium with or without serum to compare ESC harvesting efficiency. ESC derivation was also undertaken in a feeder cell-free culture system.

Results

Although ICM growth and dissociation was comparable irrespective of the media components, an enhanced ESC harvest was observed in our serum-free medium (p < 0.01). ESC harvest rate was not affected by ICM isolation technique but was attenuated in the feeder cell-free group.

Conclusion

Achieving successful techniques for human ESC research is fundamentally dependent on preliminary work using experimental animals. In this study, all experimentally developed ESC lines manifested similar features to ESCs obtained from intact blastocysts in standard culture. Cell/sera free murine ESC harvest and propagation are feasible procedures for an embryology laboratory and await refinements for translation to human medical research.


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