Adherent Cell Culture vs. Suspension Cell Culture
There are two basic systems for growing cells in culture, as monolayers on an artificial substrate (i.e., adherent culture) or free-floating in the culture medium (suspension culture).
Characteristics of Each Culture Type
Cells that are cultured in suspension can be maintained in culture flasks that are not tissue-culture treated, but as the culture volume to surface area is increased beyond which adequate gas exchange is hindered (usually 0.2 – 0.5 mL/cm2), the medium requires agitation. This agitation is usually achieved with a magnetic stirrer or rotating spinner flasks.
Adherent Cell Culture
Suspension Cell Culture
|Appropriate for most cell types, including primary cultures
||Appropriate for cells adapted to suspension culture and a few other cell lines that are nonadhesive (e.g., hematopoietic)
|Requires periodic passaging, but allows easy visual inspection under inverted microscope||Easier to passage, but requires daily cell counts and viability determination to follow growth patterns; culture can be diluted to stimulate growth
|Cells are dissociated enzymatically (e.g., TrypLE™ Express, trypsin) or mechanically
||Does not require enzymatic or mechanical dissociation
|Growth is limited by surface area, which may limit product yields
||Growth is limited by concentration of cells in the medium, which allows easy scale-up
|Requires tissue-culture treated vessel||Can be maintained in culture vessels that are not tissue-culture treated, but requires agitation (i.e., shaking or stirring) for adequate gas exchange
|Used for cytology, harvesting products continuously, and many research applications||Used for bulk protein production, batch harvesting, and many research applications
Video 3: Passaging cells
|This video explains why, when and how to passage cells grown in both adherent and suspension cultures. This includes cell dissociation, counting cells, determining optimal seeding density and preparing new culture vessels for passaged cells.