Specimen Nr. 05

Specimen:

Epineurium and Perineurium, Sciatic nerve (Rat)

Staining:

TEM

Magnification:

11 000x

Important structures :

1.Epineurium
2.Collagen fibrils of epineurium (longitudinally sliced)
3.Perineurium
4.Axon (myelin sheath of axon)
5.Fibrocyte
6.Collagen fibrils of epineurium (obliquely sliced)
Das Epineurium besteht aus straffem Bindegewebe. Die kollagenen Fibrillenbündel sind regelmäßig angeordnet und längs, quer und schräg angeschnitten. Zwischen den Faserbündeln sind Anschnitte von Zellkörpern bzw. Zellfortsätzen von Fibrozyten zu erkennen. Im Bereich des Perineuriums liegen mehrere Fibrozyten zwiebelschalenartig hintereinander, jeweils durch eine dünne Lage von Kollagenfibrillen getrennt. Das Endoneurium, das hier nicht klar zu erkennen ist, besteht aus lockerem Bindegewebe mit dünneren und unregelmäßig angeordneten kollagenen Fibrillen.

Legende:

Epineurium
Collagen fibrils of epineurium (longitudinally sliced)
Perineurium
Axon (myelin sheath of axon)
Fibrocyte
Collagen fibrils of epineurium (obliquely sliced)

Peripheral nerve (cross section)[bo]

1. Artery
2. Vein
3. Myelinated nerve fibre
4. Epineurium
5. Perineurium

Transmission electron microscope (TEM)

The sections for examination under the transmission electron microscope are about 0.1µm thick. They are referred to as ultra-thin sections.

To obtain such ultra-thin sections, the tissues are embedded in plastic polymers like epon (instead of paraffin, which is used for examination under the light microscope) after fixation and dehydration. Ultra-thin sections are not stained with dyes, but contrasted with heavy-metal salts. The heavy-metal salts lead to a different electron scatter and thereby create a differentiated blackening of the photographic negative. A common method of creating contrast results with 5% uranyl acetate and lead citrate.

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Epineurium
Collagen fibrils of epineurium (longitudinally sliced)
Perineurium
Axon (myelin sheath of axon)
Fibrocyte
Collagen fibrils of epineurium (obliquely sliced)

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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