1. Lab #6: Immunohistochemistry (IHC)
Prepared by:
El-Hindi.M. & Abdelmoneim.A.
Practical Of Histopathology
2015

2. Objective: Understand Immuonhistochemistry (IHC) Neurobiotin Calbindin
Merged image

3. Overview
Imunohistochemistry (IHC) combines histological, immunological and biochemical techniques for the identification of specific tissue components by means of a specific antigen/antibody reaction tagged with a visible label.

4. Cont.
The body's response to the introduction of a foreign agent, known as the immune response, results in the production of antibodies which bind the offending material.
Antibodies bind tightly and specifically to an "epitope" (one specific structure) on an "antigen" (foreign molecule or structure).

5. Fab region Paratope + Epitope Ab-Ag complex
The paratope is the part of an antibody which recognizes an antigen, the antigen-binding site of an antibody
An epitope, also known as antigenic determinant, is the part of an antigen that is recognized by the immune system, specifically by antibodies, B cells, or T cells.

6. Polyclonal
Ag injected into host animal. Serum collected and purified.
Multiple antibodies produced by different cell types bind multiple epitopes on Ag
Monoclonal
Ag injected into mouse. Lymphocytes isolated, hybridized.
One antibody produced by one cell type binds one epitope on Ag.

7. Cont.
An antigen can be defined as "anything that can be bound by an antibody."
This can be an enormous range of substances from simple chemicals, sugars, and small peptides to complex protein complexes such as a virus capsid.

8. Cont. Not all antigens directly elicit an antibody response.
Some require a carrier to be effective. These generally smaller antigens are called haptens.
Haptens are small molecules that elicit an immune response only when attached to a large carrier such as a protein; the carrier may be one that also does not elicit an immune response by itself.

9. Cont.
Antibodies can be generated by injecting animals with antigens, and then collecting serum after the immune response has taken place.
If the antibodies are labeled with an easily detectable molecule (a fluorescent dye, an enzyme, etc.), they become powerful detection reagents for the antigen.
This system has been exploited to generate exceptionally specific and sensitive "stains" which are used in histology as well as other disciplines.

10. Cont.
The basic process depends upon selecting an antibody sufficiently specific to bind an antigen in situ.
The antibody/antigen conjugate is then identified using a variety of signal generating molecules triggered either by the antibody/antigen interaction or by secondary processes.
The signal generators can be precipitating dyes, fluorescent molecules or electron dense (ultrastructural tag) materials for electron microscopy (EM).

12. Cont.
Immunohistochemistry is generally carried out in sectioned tissue, which allows the antibodies free access to the interior of the cells.
Immunohistochemistry can also be carried out on cells either in free solution or bound to membranes, or on monolayers of cultured cells.

13. Cont.
Intracellular Immunohistochemistry requires that the antibody to the target antigen be able to penetrate the cell membrane and whatever cell wall may be present before it can attach to the antigen.
This requires a number of steps not required for sectioned tissue.

14. Cont.
Primarily the cell membrane must be made permeable to the antibody, though at the same time the integrity of the cell contents and structures must be maintained.
This is normally achieved through the use of a specialized buffer containing a detergent.

16. Methods of antibody labeling
Direct
Indirect

17. Direct method
The antibody against the macromolecule is labeled with a fluorescent dye.
The antibody is then permitted to react with the macromolecule, and the resultant complex may be viewed with a fluorescent microscope.

18. Indirect method
a fluorescent labeled antibody is prepared against the primary antibody specific for the macromolecule of interest.
forming a secondary complex visible by fluorescent microscopy

20. Cont.
The indirect method is more sensitive than the direct method because numerous labeled anti-antibodies bind to the primary antibody, making them easier to visualize.
In addition, the indirect method does not require labeling of the primary antibody, which often is available only in limited quantities.

21. Cont.
Immunocytochemistry can be used with specimens for electron microscopy by labeling the antibody with ferritin, an electron-dense molecule, instead of with a fluorescent dye.
Ferritin labeling can be applied in both the direct and indirect methods.

23. General Immunohistochemistry Protocol

24. Part 1 Tissue preparation
1. Fixation
Fresh unfixed, fixed, or formalin fixation and paraffin embedding
2. Sectioning
3. Whole Mount Preparation

25. Part 2 pretreatment Proteolytic enzyme method and Heat-induced method
1. Antigen retrieval
Proteolytic enzyme method and Heat-induced method
2. Inhibition of endogenous tissue components
3% H2O2, 0.01% avidin
3. Blocking of nonspecific sites
10% normal serum

26. staining
Part 3
Make a selection based on the type of specimen, the primary antibody, the degree of sensitivity and the processing time required.

27. Controls It is to test for a protocol or procedure used.
Positive Control
It is to test for a protocol or procedure used.
It will be ideal to use the tissue of known positive as a control.
Negative Control
It is to test for the specificity of the antibody involved.

28. 28

30. What cellular antigens can we target?
Cytoplasmic
Nuclear
Cell membrane
Lipids
Proteins

31. Identify replicating cells

32. Locate cells that are signaling

33. Locate apoptotic cells

34. Identify activation states

35. Identify different types of cells in a tissue

36. Examine cytoskeletal structure