Specimen Nr. 02B

Specimen:

Duodenum (Human being)

Staining:

PAS-hemalaun

Magnification:

10x

Important structures :

1.Villi
2.Crypts
3.Epithelial layer of mucosa (villus)
4.Lamina propria of mucosa of villus
5.Submucosa
6.Brunner (duodenal) glands

Legende:

Villi
Crypts
Epithelial layer of mucosa (villus)
Lamina propria of mucosa of villus
Submucosa
Brunner (duodenal) glands

Villus and crypt (cross section)[bo]

1. Simple columnar epithelium with microvilli (epithelial layer of mucosa)
2. Lamina propria of mucosa
3. Goblet cell
4. Paneth's granular cells
5. Enteroendocrine (gastroenteropancreatic) cells
6. Central lymhatic vessel

PAS-Reaction

Perjodic Acid Schiff Reaction:

Structures containing carbohydrates, like glycogen and reticular fibres containing lots of glycoprotein, basal membranes, and mucins stain pink to violet. Perjodic acid splits the carbon bonds between two neighboring secondary alcohols. Then the alcohol groups are oxidized to aldehydes and are stained reddish by Schiff reagent.

Combinations with further dyes or staining techniques:

Hemalaun / Toluidine blue / Aurantia These dyes are used to stain cell nuclei.
Result: Cell nuclei turn bright blue to dark blue, depending on the dye used.
Luxol fast blue This dye is used to stain myelin sheaths. The dye has a special affinity to myelin.
Result: Myelin sheaths turn bright blue, grey matter turns pale green, and cell nuclei turn dark blue
Home
Tutor
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Magnification:

4x

Magnification:

10x

Magnification:

64x

Magnifications
Villi
Crypts
Crypts
Epithelial layer of mucosa (villus)
Lamina propria of mucosa of villus
Lamina propria of mucosa of villus
Submucosa
Brunner (duodenal) glands

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!

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