Botulinum hemagglutinin‐mediated in situ break‐up of human induced pluripotent stem cell aggregates for high‐density suspension culture
Autor: | Mee-Hae Kim, Masahiro Kino-oka, Tomohiro Tokura, Suman Chandra Nath |
---|---|
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
In situ Induced Pluripotent Stem Cells Cell Culture Techniques Cell Count Bioengineering Cell Communication Applied Microbiology and Biotechnology Suspension culture 03 medical and health sciences Bioreactors 0302 clinical medicine Antigens CD Clostridium botulinum Humans Transcellular Human Induced Pluripotent Stem Cells Induced pluripotent stem cell Cell Aggregation Chemistry Cadherins Culture Media Kinetics Hemagglutinins 030104 developmental biology Paracellular transport Biophysics Maximum Cell Density Cell bank 030217 neurology & neurosurgery Biotechnology |
Zdroj: | Biotechnology and Bioengineering. 115:910-920 |
ISSN: | 1097-0290 0006-3592 |
Popis: | Large numbers of human induced pluripotent stem cells (hiPSCs) are required for making stable cell bank. Although suspension culture yields high cell numbers, there remain unresolved challenges for obtaining high-density of hiPSCs because large size aggregates exhibit low growth rates. Here, we established a simple method for hiPSC aggregate break-up using botulinum hemagglutinin (HA), which specifically bound with E-cadherin and disrupted cell-cell connections in hiPSC aggregates. HA showed temporary activity for disrupting the E-cadherin-mediated cell-cell connections to facilitate the break-up of aggregates into small sizes only 9 hr after HA addition. The transportation of HA into the aggregates was mediated by transcellular and paracellular way after HA addition to the culture medium. hiPSC aggregates broken up by HA showed a higher number of live cells, higher cell density, and higher expansion fold compared to those of aggregates dissociated with enzymatic digestion. Moreover, a maximum cell density of 4.5 ± 0.2 × 106 cells ml-1 was obtained by aggregate break-up into small ones, which was three times higher than that with the conventional culture without aggregate break-up. Therefore, the temporary activity of HA for disrupting E-cadherin-mediated cell-cell connection was key to establishing a simple in situ method for hiPSC aggregate break-up in bioreactors, leading to high cell density in suspension culture. |
Databáze: | OpenAIRE |
Externí odkaz: |