We introduce the first lab-on-a-chip platform for complete mammalian cell culture. The new method is powered by digital microfluidics (DMF), a technique in which nanolitre-sized droplets are manipulated on an open surface of an array of electrodes. This is the first application of DMF to adherent cell culture and analysis, and more importantly, represents the first microfluidic platform capable...

Cells have been established in continuous culture from human and animal tissues, both normal and carcinomatous. From 197 specimens, 105 could be maintained in vitro for varying lengths of time, 27 for more than 6 months. In all cases the cells were found to be diploid. Cell lines with both epithelial and fibroblastic morphology have been isolated in medium 199 with added fetal calf serum, but a...

Microfluidic perfusion cultures for mammalian cells provide a novel means for probing single-cell behavior but require the management of culture parameters such as flow-induced shear stress. Methods to eliminate shear stress generally focus on capturing cells in regions with high resistance to fluid flow. Here, we present a novel trapping design to easily and reliably load a high density of cel...

Microwell arrays have emerged as robust and versatile alternatives to conventional mammalian cell culture substrates. Using standard microfabrication processes, biomaterials surfaces can be topographically patterned to comprise high-density arrays of micron-sized cavities with desirable geometry. Hundreds to thousands of individual cells or cell colonies with controlled size and shape can be tr...

BACKGROUND Protein aggregation during monoclonal antibody (mAb) production can occur in upstream and downstream processing (DSP). Current methods to determine aggregate formation during cell culture include size exclusion chromatography (SEC) with a previous affinity chromatography step in order to remove disturbing cell culture components. The pre-purification step itself can already influence...

Eagle showed that a medium containing the 13 amino acids and the seven vitamins found to be essential for the growth of L and HeLa cells, each at the optimum concentration and appropriately supplemented with glucose, does not permit growth unless a small amount of serum was added (Eagle, 1973). Therefore it has been suggested that serum contains macromolecular factors required for multiplicatio...

Albumin has a long historical involvement in design of media for the successful culture of mammalian cells, in both the research and commercial fields. The potential application of albumins, bovine or human serum albumin, for cell culture is a by-product of the physico-chemical, biochemical and cell-specific properties of the molecule. In this review an analysis of these features of albumin lea...

Aryl hydroxylase, derived from hamster fetus cells grown in culture, is an inducible microsomal enzyme system which requires NADPH and molecular oxygen. The addition of benz[u]anthracene or other polycyclic hydrocarbons to the culture medium causes significant increases in the amount of hydroxylase activity: after a lag period of 35 min, the level of hydroxylase activity increases linearly for ...

There are numerous approaches for producing natural and synthetic 3D scaffolds that support the proliferation of mammalian cells. 3D scaffolds better represent the natural cellular microenvironment and have many potential applications in vitro and in vivo. Here, we demonstrate that 3D cellulose scaffolds produced by decellularizing apple hypanthium tissue can be employed for in vitro 3D culture...

Engineering spatial patterning in mammalian cells, employing entirely genetically encoded components, requires solving several problems. These include how to code secreted activator or inhibitor molecules and how to send concentration-dependent signals to neighboring cells, to control gene expression. The Madin-Darby Canine Kidney (MDCK) cell line is a potential engineering scaffold as it forms...