The class III beta-tubulin isotype is widely used as a neuronal marker
in normal and neoplastic tissues. This isotype was, however, also imm
unodetected in certain tumours of non-neuronal origin such as squamous
cell carcinoma. Using a newly described monoclonal antibody we compar
ed the distribution of class III beta-tubulin in normal and neoplastic
tissues, The TU-20 mouse monoclonal antibody was prepared against a c
onserved synthetic peptide from the C-terminus of the human class III
beta-tubulin isotype, and its specificity was confirmed by immunoblott
ing, by competitive enzyme-linked immunosorbent assay and by immunoflu
orescence microscopy on cultured cells. In different cell lines of var
ious origins the antibody reacted only with neuroblastoma Neuro-2a cel
ls and with embryonal carcinoma P19 cells stimulated to neuronal diffe
rentiation by retinoic acid. Immunohistochemistry on formaldehyde-fixe
d paraffin-embedded normal human tissues revealed the presence of the
class III beta-tubulin isotype in cell bodies and processes of neurona
l cells in the peripheral and central nervous systems. In other tissue
s, this beta-tubulin isotype was not immunodetected. Class III beta-tu
bulin was found in all cases of ganglioneuroblastoma, ganglioneuroma,
medulloblastoma, neuroblastoma, sympathoblastoma and in one case of te
ratoma. In contrast, no reactivity was detected in tumours of non-neur
onal origin, including 32 cases of squamous cell carcinoma. The result
s indicate a specific TU-20 epitope expression exclusively in neuronal
tissues. The antibody could thus be a useful tool for the probing of
class III beta-tubulin functions in neurons as well as for immunohisto
chemical characterisation of tumours of neuronal origin.