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Cited 2 time in webofscience Cited 4 time in scopus
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Fabrication of size-controllable human mesenchymal stromal cell spheroids from micro-scaled cell sheets

Authors
Byun, HayeonLee, Yu BinKim, Eun MiShin, Heungsoo
Issue Date
Jul-2019
Publisher
IOP PUBLISHING LTD
Keywords
microcontact printing; thermosensitive hydrogel; size-controlled spheroid; mesenchymal stem cell
Citation
BIOFABRICATION, v.11, no.3
Indexed
SCIE
SCOPUS
Journal Title
BIOFABRICATION
Volume
11
Number
3
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/4548
DOI
10.1088/1758-5090/ab21f6
ISSN
1758-5082
Abstract
Recently, stromal cell spheroids have been actively studied for use in tissue regeneration. In this study, we report a method for the fabrication of size-controllable stromal cell spheroids in different sizes from micro-scaled cell sheets (mu CS) using thermosensitive hydrogels and investigated their effects on stromal cell function. Mesenchymal stromal cells isolated from different tissues such as human turbinate tissue, bone marrow, and adipose tissue were adhered selectively to each micro-pattern (squares with widths of 100 and 400 mu m) on the surface of the hydrogel and formed mu CS. The diameters of the spheroids were modulated by the size of the patterns (45 +/- 5 and 129 +/- 4 mu m in diameter for the 100 and 400 mu m micro-patterns, respectively) and the seeding density (129 +/- 4, 149 +/- 6, and 163 +/- 6 mu m for 5.0, 10.0, and 15.0 x 10(4) cells cm(-2), respectively, on 400 mu m micropattern). In addition, the spheroids were successfully fabricated regardless of stromal cell origin, and the diameter of the spheroids was also affected by cell spreading area on a cell culture dish. Stemness markers were highly expressed in the spheroids regardless of the spheroid size. Furthermore, an increase in E-cadherin and decrease in N-cadherin gene expression showed the stable formation of spheroids of different sizes. Gene expression levels of hypoxia inducible factors and secretion of vascular endothelial growth factor were increased (13.2 +/- 1.4, 325 +/- 83.4 and 534.3 +/- 121.5 pg ng(-1) DNA in a monolayer, and 100 and 400 mu m micro-patterned spheroids, respectively) proportional to the diameters of the spheroids. The size of spheroids were maintained even after injection, cryopreservation and 7 d of suspension culture with high viability (similar to 90%). In conclusion, this novel technique to fabricate spheroids with controlled size could be widely applied in various applications that require a controlled size in regenerative medicine.
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