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Protocol for Caco-2 cell culture

Author: Arun Malik and Hariom Yadav*
Affiliation: Nutritional Biotechnology Department, National Agri-Food Biotechnology Institute, Mohali, India
Source: Protocol Online
Date Added: Tue Jan 22 2013
Date Modified: Tue Jan 22 2013
Abstract: This protocol describes about how Caco2 cells should be maintained into the labs and common cares which should be taken during culture process.

Introduction
Cell culture is very important approach to investigate various molecular mechanism(s) and phenotypes in cells that are distinct or separated from whole animal system. Caco-2 cells are continuous lines of heterogenous human epithelial colorectal adenocarcinoma cells. These cells are derived from human large intestine and become differentiated and polarized like small intestinal cells, when grown in specific cell culture conditions. Caco-2 cells from American Type Culture Collection (ATCC) grown in basic culture medium in tissue culture flasks/discs. Normally cultures kept at 37°C in a 5% CO2/95% air atmosphere. Caco-2 cells are mostly used as a confluent monolayer on a cell culture inserts filters. The Caco-2 monolayer is widely used across the pharmaceutical industry as an in vitro model of human small intestinal mucosa to predict the absorption of orally administered drugs. We are discussing a protocol which can be normally adopted to culture and maintain these cell lines in the laboratories.
 

Materials and reagents

Procedure

  1. Cacao-2 cells cultures routinely maintained in tissue culture flasks/ discs in Dulbecco’s Modified Eagle Medium (DMEM) medium containing 10% Fetal Bovine Serum (FBS) and 1% penicillin-streptomycin.
  2. Cells split into 2.5x10 cm flasks/discs every 3-4 days with re-feeding of every 48-72 hours.
  3. Remove culture medium from flasks/discs and wash monolayer with 1x Phosphate Buffer Saline (PBS).
  4. Add 2-5 ml of trypsin solution; incubate at 37°C for 1-4 minutes to remove the cells from surface.
  5. Add 15 ml of DMEM supplemented with 10% FBS and 1% P/S media to inactivate trypsin and thoroughly pipette up and down to break the cell clumps.
  6. Transfer required volume of warm media to seed cells in a sterile flask/disc.
  7. If required count the cells using standard cell counting procedure (described somewhere else).
  8. Excess cells may be re-seeded in to a new flask. Every time cells are passaged and the passage number increased by 1.
  9. The media usually changed every 48-72 hours by aspirating off old media and replace it with new media.
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