Specimen Nr. 06E

Specimen:

Spleen (Rat), immunologic reaction, secondary follicle

Staining:

Alkaline-phosphatase technique, nucleus stained with hemalaun

Magnification:

150x

Important structures :

1.	Central artery
2.	Periarteriolar lymphoid sheath (PALS)
3.	Germinal centre of a lymphoid follicle (secondary follicle)
4.	Corona of a secondary lymphoid follicle
5.	Marginal zone of white pulp
6.	Red pulp

Mit Antikörpern sind immunhistochemisch in rot alle Zellen dargestellt, die sich im Zellzyklus befinden. Die meisten proliferierenden Lymphozyten findet man im Keimzentrum eines Sekundärfollikels. Die Milz einer gesunden Laborratte enthält nur wenige Sekundärfollikel mit Keimzentren.

Legende:

	Central artery
	Periarteriolar lymphoid sheath (PALS)
	Germinal centre of a lymphoid follicle (secondary follicle)
	Corona of a secondary lymphoid follicle
	Marginal zone of white pulp
	Red pulp

Immunohistochemestry

Immunohistochemistry is used to confirm the presence of or to identify certain structures or substances in tissue sections which cannot be identified with conventional staining methods. Such structures include: cells, enzymes, hormones, macromolecules like nucleic acids and polysaccharides. The basis of immunohistochemical staining techniques is the antigen-antibody reaction. This method makes it possible to differentiate, for example, various cells in a tissue section according to their different metabolic products or surfaces. Either the metabolic product or a certain surface component serves as the antigen. In the first step, the antigen reacts with a specific antibody. The resulting antigen-antibody complex is invisible. Therefore, in a further step a second antibody bound to an adjuvant is added and binds to the initial antibody (so-called sandwich procedure). The bound adjuvant makes the antigen-antibody complex visible under the microscope and identifies the sought structure. Adjuvants are:

fluorescent dyes:
fluoresce by stimulation under UV light
enzymes:
catalyze a definite dye reaction
particular markers:
The immune complexes can be made visible with, e.g. bound gold particles, both in direct light and under the electron microscope.
radionuclids:
The substance sought is identified by blackening a photographic plate or an applied photo film.

Combination with further dyes or staining techniques:

hemalaun
dye for staining cell nuclei
result: Cell nuclei turn an intense blue.

HistoNet2000 - Help

1. Organization of the screen surface

Right side: histologic specimen
Left side: information about the specimen (above) and general program functions (below)

2.Histologic specimen

Pull the mouse across the histologic specimen for training purposes. A small square with exclamation marks (dynamic labels) will appear where there is an important structure. You should then decide what structure this could be. To check your result, simply click the appropriate square, and the correct label will appear. The option “marked” allows you to see all labels for all structures simultaneously. These can be removed by clicking “unmarked”. This reactivates the dynamic labels.

3. Complementary information

Info: general information about the specimen, as well as a list of the dynamic labels
Drawing: schematic drawing of the specimen
Staining: information about the staining method for this specimen
Knowledge: short texts with basic histologic information, presently deactivated

4. General Program Functions

Home: returns you to the “start” page
Tutor: how to contact the HistoNet Team
Help: Instructions for Use appear
Exit: closes down the HistoNet program
Boxes: goes back to the other specimen of a topic
VM: provides virtual microscopy

We hope you will enjoy working with HistoNet2000 and learn a lot from it!