Although cytoskeleton is a ubiquitous intracellular system, several cytoskeletal proteins can be used as tissue specific markers, namely to indicate neural tissues.
The class III isoform of β-tubulin is present dominantly in cells of neuronal origin and it is one of the earliest markers of neuronal differentiation.
Microtubule associated proteins 2a and 2b stabilize microtubules mainly in dendrites. They participate in determining the structure of different parts of vertebrate nerve cells.
Neurofilaments, the type of intermediate filaments expressed almost exclusively in neuronal cells, are abundant in large axons. In most vertebrates they are composed of three different polypeptide chains – neurofilament heavy, medium and light protein, which are for their high stability very useful neuronal markers.
Glial fibrillary acidic protein is the principal marker of astroglial cells in the central nervous system, which is specifically expressed in satellite cells in peripheral ganglia and in non myelinating Schwann cells in peripheral nerves. Fig. 1: Immunocytochemistry staining of P-19 murine embryonal carcinoma cell line stimulated to neuronal differentiation by retinoic acid. A - Microtubules decorated with neuron-specific anti-betaIII-tubulin (TU-20; red). B - Merged image of co-staining with anti-beta-tubulin (TU-06; green; cat. no. 11-251-C100). Superposition of red and green colours provided yellow staining. Nuclei were stained with DNA-binding dye (blue). Fig. 2: Immunohistochemistry staining of human cerebellum (paraffin-embedded sections) with anti-neurofilament heavy protein (NF-01). Fig.3: Immunohistochemistry staining of human cerebellum (paraffin-embedded sections) with anti-GFAP (clone GF-01).
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Today we bring an extension to the Notch topics presented in previous blog.
Notch signaling represents one of the cornerstones of the immune system.
Anti-human CD38 clones HB7 and HIT2 were compared regarding their reactivity with particular blood cell populations.