2011 Lab 9
- 1 Tissue Culture 1
- 1.1 Introduction
- 1.2 Objectives
- 1.3 Cell Biology Handbook
- 1.4 Types of Cell Culture
- 1.5 Culture Method
- 1.6 Contamination
- 1.7 Cell Growth
- 1.8 Cell Analysis
- 1.9 References
- 1.10 Supplier Information
- 1.11 Links
- 1.12 Terms
- 1.13 2012 Course Content
Tissue Culture 1
A general tutorial introduction to cell culture techniques in Cell Biology.
Before beginning any research:
- You should be aware and understand the legal and ethical issues related to research practice.
- Joint NHMRC / AVCC Statement and Guidelines on Research Practice (1997)
- See also Primary Tissue Culture
- You should be aware and understand all Occupational Health and Safety (OHS) issues that relate to your project.
- Understand the use and limitations of in vitro cell analysis
- Understand the basic requirements for a tissue culture laboratory
- Understand the basic techniques of tissue culture, sterile technique, contamination analysis, bio-waste, cell storage
- Understanding the differences between primary and cell line cultures
- Brief understanding of cell growth requirements
- Brief understanding of analytical techniques
Cell Biology Handbook
This online publication by ECACC gives a good general introduction to tissue culture techniques. ECACC Handbook
I have also provided a brief 4 page handout to introduce the topic giving a broad historic background and some relevant sections from cell biology texts.
Types of Cell Culture
Also called Continuous Cultures. Cell lines may be established or generated by individual research groups or available from a larger cell supplier (bank). There are two main suppliers worldwide of cell lines, ATCC and ECACC. Different cell lines will have different growth properties, passage-ability and characterization.
American Type Culture Collection - ATCC
"...global nonprofit bioresource center that provides biological products, technical services, and educational programs to private industry, government, and academic organizations around the world. Our mission is to acquire, authenticate, preserve, develop, and distribute biological materials, information, technology, intellectual property, and standards for the advancement, validation, and application of scientific knowledge.
- ATCC was established in 1925 when a committee of scientists recognized a need for a central collection of microorganisms that would serve scientists all over the world. The early years were spent at the McCormick Institute in Chicago until the organization moved to Georgetown University in Washington, DC in 1937. As research in the biosciences expanded, ATCC began to diversify its holdings, and as the collections grew ATCC occupied a series of sites, each providing more storage space. ATCC moved to its current state-of-the-art building in 1998.
- ATCC USA
- Bacteria, Bacteriophages, Cell Lines and Hybridomas, Filamentous Fungi and Yeast Plant Seeds, Protozoa and Algae, Viruses and Antisera.
- Cultures and Products
European Collection of Cell Cultures - ECACC
"The European Collection of Cell Cultures (ECACC) was established in 1984 as a cell culture collection to service the research community and provide an International Depository Authority recognised patent depository for Europe." "The collections currently hold over 40,000 cell lines representing 45 different species, 50 tissue types, 300 HLA types, 450 monoclonal antibodies and at least 800 genetic disorders."
- European Collection of Cell Cultures (ECACC), a Health Protection Agency Culture Collection.
- ECACC Europe
- General Cell Collection
- ECACC Handbook
- Primary cell cultures are derived from rat, mouse and human in the Lab. The majority of cultures focus on the growth of either neurons and/or glia. Cultures can be generated from embryonic or adult: cortex, retina, spinal cord, dorsal root ganglia, sympathetic ganglia. Depending on the preparation technique either neurons, glia or neurons and glial cultures can be generated.
- primary cell culture refers to the cells the first time they are placed in culture.
- Once these cells have been subcultured are no longer primaries and should not be described as primary culture.
- The advantages of primary cultures are that the cells have not been "modified" in any way (other than enzymatic or physical dissociation).
- The disadvantages of primary cultures are the mixed nature of each preparation, limited lifespan of the culture and the potential contamination problems. In some cases these cells can also be stored frozen for future use.
- Remember that in the adult (except for olefactory and ventricular) neurons are post-mitotic and will not proliferate unless transformed.
- All primary cell culture experiments using animals need Animal Ethics approval and must comply with Australian Code of Practice for the Care and Use of Animals for Scientific Purposes, National Health and Medical Research, Council (6th edn, 1997).
- All primary cell culture experiments using human material need Human Ethics approval.
- cells grow until they cover the surface area available or the medium is depleted of nutrients
- some cells are "contact inhibited"
- once a monolayer is formed and cells contact each other, they cease proliferation
- these cells will need to be separated from the substrate
- mechanically (scraper)
- enzymatically (trypsinization)
- both enzymatic and mechanical
- mixed population of cells some adherent and some in suspension
- both cell populations need to be preserved in passaging
- not a common culture
- cell cultures derived from blood (e.g. lymphocytes)
- grow in suspension, not adherent to a sustratum
- some cell lines may grow as single cell suspensions or in clumps (e.g. EBV transformed lymphoblastoid cell lines)
- clumping cells may require centrifugation and resuspension by pipetting generate a single cell suspension (for counting)
- Infection can: alter of growth rate, induce of morphological changes, lead to chromosomal aberrations, alter cell metabolism and decrease viability upon resuscitation of frozen ampoule. EEACC Mycoplasma Testing
- Detected by PCR, DNA Stain or Culture Isolation.
- ATCC Mycoplasma
Basic Constituents of media, inorganic salts, buffering systems, carbohydrates, vitamins, proteins/peptides, fatty acids/lipids, trace elements.
- cells require pH conditions in the range 7.2 - 7.4 and close control of pH.
- phenol red acts as a pH indicator, culture medium should be changed if the color turns yellow (acid) or purple (alkali).
- bicarbonate/CO2 buffering systems need to be maintained in incubator atmosphere of 5-10% CO2.
- Heat inactivation - involves heating at 56°C for 1 hour to inactivate complement components and prevent the occurrence of complement mediated lysis in cell cultures.
- Safety testing - different between countries: No safety testing required (USA/Canada, New Zealand, Finland and Denmark), Safety testing may be required (Australia, Mexico, Central America).
Cells can be analysed in many different experimental techniques
- Living or Fixed
- Time lapse
- Confocal microscopy
- In Situ hybridization
- DNA (Southern)
- mRNA (Northern)
- Protein (Western)
- Flow cytometry
Molecular Biology of the Cell
Alberts, Bruce; Johnson, Alexander; Lewis, Julian; Raff, Martin; Roberts, Keith; Walter, Peter New York and London: Garland Science; c2002
Growth Factor Model Image: MBoC Ch18 Fig 45 MCB Figure 6-5. Stages in the establishment of a cell culture. Image: MBoC Ch18 Fig 46/47
- Some Landmarks in the Development of Tissue and Cell Culture
- Cells Can Be Grown in a Culture Dish
- Serum-free, Chemically Defined Media Permit Identification of Specific Growth Factors
Molecular Cell Biology
Lodish, Harvey; Berk, Arnold; Zipursky, S. Lawrence; Matsudaira, Paul; Baltimore, David; Darnell, James E. New York: W. H. Freeman & Co.; c1999
The Cell- A Molecular Approach
Cooper, Geoffrey M. Sunderland (MA): Sinauer Associates, Inc.; c2000
Search Online Textbooks
- "cell+culture" Bookshelf
- PubMed is a service of the U.S. National Library of Medicine that includes over 18 million citations from MEDLINE and other life science journals for biomedical articles back to 1948. PubMed includes links to full text articles and other related resources. PubMed
- PubMed Central (PMC) is a free digital archive of biomedical and life sciences journal literature at the U.S. National Institutes of Health (NIH) in the National Library of Medicine (NLM) allowing all users free access to the material in PubMed Central. PMC
- Online Mendelian Inheritance in Man (OMIM) is a comprehensive compendium of human genes and genetic phenotypes. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes. OMIM
- Entrez is the integrated, text-based search and retrieval system used at NCBI for the major databases, including PubMed, Nucleotide and Protein Sequences, Protein Structures, Complete Genomes, Taxonomy, and others Entrez
- Animal Cell Culture: A Practical Approach ed R.I Freshney
Polyethyleneimine - attachment factor for weakly anchoring cell lines and primary cells. Used in lipofection protocols, more reliable and increases the yield of expressed products with commonly used cell lines such as PC-12 and HEK-293 cells.
sterile (aseptic) technique - carrying out tissue culture procedures without introducing contaminating microorganisms from the environment.
2012 Course Content
Lectures: Cell Biology Introduction | Cells Eukaryotes and Prokaryotes | Cell Membranes and Compartments | Cell Nucleus | Cell Export - Exocytosis | Cell Import - Endocytosis | Cell Mitochondria | Cell Junctions | Cytoskeleton Introduction | Cytoskeleton - Intermediate Filaments | Cytoskeleton - Microfilaments | Cytoskeleton - Microtubules | Extracellular Matrix 1 | Extracellular Matrix 2 | Cell Cycle | Cell Division | Cell Death 1 | Cell Death 2 | Signal 1 | Signal 2 | Stem Cells 1 | Stem Cells 2 | 2012 Revision | Development
Laboratories: Introduction to Lab | Microscopy Methods | Preparation/Fixation | Immunochemistry | Cell Knockout Methods | Cytoskeleton Exercise | Confocal Microscopy | Microarray Visit | Tissue Culture 1 | Tissue Culture 2 | Stem Cells Lab | Stem Cells Analysis
|2012 Projects: Group 1 | Group 2 | Group 3 | Group 4 | Group 5 | Group 6 | Group 7 | Group 8 | Group 9|
Dr Mark Hill 2015, UNSW Cell Biology - UNSW CRICOS Provider Code No. 00098G