Cytology · MU Sofia

8. Cell culture.

Explains cell culture as a way of growing living cells outside the body in a controlled artificial setting. Covers the key components, including primary cells versus permanent cell lines such as HeLa, culture medium, incubators and sterile technique, then the basic steps from isolation and seeding to subculturing. Also lists applications such as vaccine production and drug testing, and summarises microscopy methods for viewing cultured cells: phase-contrast, differential interference and fluorescence.

Inside: 1 section · 2 labelled pictures · 16 flashcards · 6 min

Topic 8 of 97 in the MU Sofia syllabus for Cytology (Medicine, Year 1). The free AceMed note covers it in 1 section, about 883 words (6 min of reading), with 16 flashcards.

In this note

  1. Introduction

Introduction

Cell Culture

Cell culture, also known as tissue culture, is a laboratory technique used to cultivate and maintain living cells outside their natural environment. This technique involves growing cells in a controlled, artificial environment that mimics the conditions required for their growth and proliferation.

Cell culture is a fundamental tool in various fields, including biomedical research, drug development, and biotechnology.

Key Components and Steps in Cell Culture

Here are the key components of cell culture:

Cell Lines: Cell culture requires a source of cells, which can be primary cells isolated directly from a tissue or cell lines.

Cell lines are populations of cells adapted to grow continuously in culture and are often derived from tumors or other specialized sources.

Primary cells, on the other hand, have a limited lifespan in culture.

Culture Medium: Cells are grown in a culture medium, which provides essential nutrients, such as amino acids, vitamins, minerals, and growth factors.

The specific composition of the medium varies depending on the cell type being cultured and the research goals.

Incubator: Cells are cultured in incubators that maintain a controlled environment, including temperature, humidity, and carbon dioxide levels.

This controlled environment mimics the cells' physiological environment.

Sterile Techniques: Maintaining sterility is crucial to prevent contamination by microorganisms.

Researchers use laminar flow hoods and strict protocols to ensure a sterile environment.

The basic steps involved in cell culture are as follows:

Cell Isolation: When using primary cells, they must be isolated from a tissue sample using mechanical and enzymatic methods.

Seeding: Cells are seeded onto culture vessels, such as petri dishes or flasks, containing culture medium.

The seeding density, or number of cells added per unit area, is important and depends on the experiment.

Incubation: Culture vessels are placed in an incubator to maintain optimal conditions for cell growth.

Subculturing: As cells grow and cover the surface of the culture vessel (become confluent), they need to be subcultured or passaged.

This involves detaching cells and transferring them to new vessels to prevent overgrowth and maintain cell health.

Experimental Manipulations: Researchers can perform various experiments on the cells in culture, such as introducing treatments or drugs and studying cellular responses.

Applications of Cell Culture

Cell culture has a wide range of applications, including:

Biomedical Research: Cell culture is crucial for understanding basic cell biology, disease mechanisms, and developing therapies.

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