Specialist Course on Light and Fluorescence Microscopy edition 2022

PhD students with limited experience in light microscopy who (will) make extensive use of microscopic visualization techniques for life science research applications (in the near future). No prior experience or training is required.

Light microscopy, and especially fluorescence microscopy, is an essential tool to investigate and characterize biological specimen in the life sciences. Modern microscopes offer an increasing range of technical capabilities, but thereby become gradually more complex and require appropriate training for correct scientific use. This specialist course provides doctoral students with limited experience in microscopic imaging with the understanding that is needed to perform light and confocal imaging at a research-grade level.

• Day 1: Theoretical session (September 7, 2022 from 9 – 12 a.m.)

Lecture 1: Fundamentals of light and imaging – prof. Kevin Braeckmans
The main physical principles involved in image formation are explained. After reviewing concepts as light refraction, diffraction, resolution, etc., the basics of image formation are addressed. The differences between the types of objective lenses are discussed and attention is drawn to correct sample illumination.

Lecture 2: Transmitted light microscopy and digital imaging – Geert Meesen
The visualization of cells often proves to be difficult. The use of dedicated illumination techniques can enhance the image quality significantly. This lecture furthermore focuses on contrast-enhancing techniques such as DIC and phase contrast microscopy that help to reveal the smallest details in a cell. Concepts as resolution and noise are explored further and  guidelines involving correct camera use and the impact of digital imaging are offered.

• Day 1: Demonstration sessions (September 7,  2022 from 1 – 5 p.m.)

Transmitted light microscopy – Dr. Herlinde De Keersmaecker, Geert Meesen, Zeiss
In the first demonstration session cell visualization with transmitted light microscopy is covered. The participants will learn in groups of 5 to set the correct sample illumination and explore different transmitted light microscopy techniques. The advantages of different contrast-enhancing techniques will be demonstrated and the principles of digital imaging are put into practice.

• Day 2: Theoretical session (September 8, 2022 from 9 – 12 a.m )

Lecture 1-2: Epi-fluorescence and confocal imaging – prof. Winnok De Vos
Fluorescence microscopy allows to image specific parts of a specimen with unrivalled contrast. In this session the basic concepts underlying fluorescence imaging are reviewed. It is explained how, with the use of various confocal techniques, optical slicing and three-dimensional imaging is achieved. Furthermore it is pointed out that the combination of confocal imaging and spectral detection is an excellent way to differentiate between different subunits in a sample. Special attention is drawn to practical considerations that are inherent to confocal microscopy, such as photobleaching and bleed-through.

Lecture 3: Cell labelling and considerations for live cell imaging – Dr. Herlinde De Keersmaecker
This lecture explores the different properties of fluorescent labels and discusses the practical considerations when used for life science research. Different techniques used to introduce fluorescent dyes into a specific structure of both fixed and living cells are discussed. Attention is given to creating optimal conditions for live cell imaging.

• Day 2: Demonstration session (September 8, 2022 from 1 – 5 p.m.)

Fluorescence and confocal imaging – Dr. Herlinde De Keersmaecker, Geert Meesen, representative industry (Nikon)
The concepts of epi-fluorescence microscopy and confocal imaging will be shown. Each session will demonstrate and focus on a specific capability and the related caveats of fluorescence imaging methods covered during the theoretical lectures with as goal to develop a correct scientific way of microscopic imaging. In between the demonstration sessions, two moments are foreseen to discuss and apply the new insights to a selection of their own research questions in small groups of 5 students. During the demonstrations time is foreseen to discuss questions from the peer assistant learning session related to the demonstration.

• Day 3: Demonstration and peer assistant learning session (September 9, 2022 from 9 – 11 a.m.)

Fluorescence and confocal imaging – Dr. Herlinde De Keersmaecker, Geert Meesen, representative industry (Nikon)
The concepts of epi-fluorescence microscopy and confocal imaging will be shown. Each session will demonstrate and focus on a specific capability and the related caveats of fluorescence imaging methods covered during the theoretical lectures with as goal to develop a correct scientific way of microscopic imaging. In between the demonstration sessions, two moments are foreseen to discuss and apply the new insights to a selection of their own research questions in small groups of 5 students. During the demonstrations time is foreseen to discuss questions from the peer assistant learning session related to the demonstration.

• Day 3: Peer assistant learning session (September 9, 2022 from 11 a.m. – 1 p.m.)

Each group of 5 students gives a 5-10 min presentation of the results of their discussion followed by a short Q&A session with all participants.

• Day 3: Guided computer session (September 9, 2022 from 14 – 17 p.m.)

Basics of image processing – Geert Meesen, Dr. Herlinde De Keersmaecker
Using a set of microscopy images, the fundamentals of image processing and quantitative image analysis are explained through a guided computer session. The session provides basic understanding and application of FIJI, an open source image processing platform widely used in biomedical research.