TY - JOUR
T1 - Effect of cooling stimulus on collection efficiency of calf chondrocytes cultivated on metal surface
AU - Kurashina, Yuta
AU - Miyata, Shogo
AU - Komotori, Jun
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Numbers JP15H03547.
Publisher Copyright:
© 2017, Fuji Technology Press. All rights reserved.
PY - 2017/11
Y1 - 2017/11
N2 - A cell culture module capable of cooling stimulus to collect cells efficiently on a metal culture substrate was developed. We evaluated the cell collection ratio and morphology of the collected cells. Following a cooling stimulus (0◦ C) for 20 min, the number of collected cells was increased by 50% compared to that collected after trypsin treatment without pipetting from the metal culture substrate. Following the cooling stimulus, cells were observed by fluorescence microscopy and scanning electron microscopy; the cell filopodia were shrunken compared to non-cooling-stimulated cells. Furthermore, the combination of collagenase and cooling stimulation resulted in the collection of a comparable number of cells as that obtained using only trypsin. Thus, cell proliferation was improved compared to that following trypsin treatment. Therefore, this method can be applied for culturing cells that are susceptible to trypsin damage.
AB - A cell culture module capable of cooling stimulus to collect cells efficiently on a metal culture substrate was developed. We evaluated the cell collection ratio and morphology of the collected cells. Following a cooling stimulus (0◦ C) for 20 min, the number of collected cells was increased by 50% compared to that collected after trypsin treatment without pipetting from the metal culture substrate. Following the cooling stimulus, cells were observed by fluorescence microscopy and scanning electron microscopy; the cell filopodia were shrunken compared to non-cooling-stimulated cells. Furthermore, the combination of collagenase and cooling stimulation resulted in the collection of a comparable number of cells as that obtained using only trypsin. Thus, cell proliferation was improved compared to that following trypsin treatment. Therefore, this method can be applied for culturing cells that are susceptible to trypsin damage.
KW - Cell adherence
KW - Cell proliferation
KW - Chondrocyte
KW - Fine particle peening
KW - Surface modification
UR - http://www.scopus.com/inward/record.url?scp=85035071519&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85035071519&partnerID=8YFLogxK
U2 - 10.20965/ijat.2017.p0925
DO - 10.20965/ijat.2017.p0925
M3 - Article
AN - SCOPUS:85035071519
SN - 1881-7629
VL - 11
SP - 925
EP - 931
JO - International Journal of Automation Technology
JF - International Journal of Automation Technology
IS - 6
M1 - ijate001100060925
ER -