Laser-assisted cell removing (LACR) technology contributes to the purification process of the undifferentiated cell fraction during pluripotent stem cell culture
Creators
- 1. Department of Obstetrics and Gynecology, Mie University Graduate School of Medicine (Japan)
- 2. Division of Cell Biology for Regenerative Medicine, Institute of Advanced Clinical Medicine, Kindai University Faculty of Medicine, Osaka (Japan)
- 3. Sinfonia Technology Co. Ltd. (Japan)
- 4. Kindai University Life Science Research Institute, Kindai University (Japan)
- 5. Laboratory of Embryonic Stem Cell Research, Institute for Frontier Life and Medical Sciences, Kyoto University (Japan)
Description
Highlights: • Purification of undifferentiated cells is a critical step in stem cell culture. • We developed an automated laser-assisted cell removing technology. • This system successfully removed contaminated/differentiated cells in human iPS cell culture. Purification of undifferentiated cells by removing differentiated parts is an essential step in pluripotent stem cell culture. This process has been traditionally performed manually using a fine glass capillary or plastic tip under a microscope, or by culturing in a selective medium supplemented with anti-differentiation inhibitors. However, there are several inevitable problems associated with these methods, such as contamination or biological side-effects. Here, we developed a laser-assisted cell removing (LACR) technology that enables precise, fast, and contact-less cell removal. Using LACR combined with computational image recognition/identification-discriminating technology, we achieved automatic cell purification (A-LACR). Practicability of A-LACR was evaluated by two demonstrations: selective removal of trophoblast stem (TS) cells from human iPS and TS cell co-cultures, and purification of undifferentiated iPS cells by targeting differentiated cells that spontaneously developed. Our results suggested that LACR technology is a novel approach for stem cell processing in regenerative medicine.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2018.08.101Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2018.08.101;
- PII
- S0006291X18317856;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 503
- Journal Issue
- 4
- Journal Page Range
- p. 3114-3120
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53051491
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CAPILLARIES; CELL CULTURES; DRUGS; SIDE EFFECTS; STEM CELLS
- Descriptors DEC
- ANIMAL CELLS; BLOOD VESSELS; BODY; CARDIOVASCULAR SYSTEM; ORGANS; SOMATIC CELLS
Optional Information
- Copyright
- Copyright (c) 2018 The Authors. Published by Elsevier Inc.