Hirano bodies are intracellular aggregates of actin and actin-associated proteins first observed in neurons (nerve cells) by Asao Hirano in 1965.[1] The eponym ‘Hirano bodies’ was not introduced until 1968, by Schochet et al., three years after Hirano first observed the proteins.[2]
Hirano bodies were first described in the CA1 in patients with amyotrophic lateral sclerosis and parkinsonism-dementia complex (ALS-PDC).[2] Hirano bodies (Hb) are found mostly in the neuronal processes in the pyramidal layer in the Sommer’s sector (CA1) of the hippocampus, mostly arising from age related changes in the microfilament system.[2][4] Hirano bodies are often described as rod-shaped, crystal-like, and eosinophilic (pink after staining with haematoxylin and eosin). They are frequently seen in hippocampal pyramidal cells.[5] An experimental model of Hirano body formation has been reported, using a genetically altered strain of the slime moldDictyostelium discoideum.[6]
Hirano bodies have been noted as a function of age without obvious underlying neurodegeneration.[7]
^University of EdinburghArchived 2013-10-02 at the Wayback Machine, Hirano bodies, citing Hirano, Asao. (1965) "Pathology of amyotrophic lateral sclerosis," in Slow Latent and Temperate Virus Infections, National Institute of Neurological Diseases and Blindness (NINDB) monograph No.2, pp. 23-37.
^Schmidt, M. L.; Lee, V. M.; Trojanowski, J. Q. (1989). "Analysis of epitopes shared by Hirano bodies and neurofilament proteins in normal and Alzheimer's disease hippocampus". Lab. Invest. 60 (4): 513–522. PMID2468822.
^Maselli, A. G., Davis, R., Furukawa, R. and Fechheimer, M. (2002)."Formation of Hirano bodies in Dictyostelium and mammalian cells induces by expression of a modified form of an actin-crosslinking protein," J.Cell Sci. 115, 1939-1952.
^Gibson, P. H.; Tomlinson, B. E. (1977). "Numbers of Hirano bodies in the hippocampus of normal and demented people with Alzheimer's disease". J. Neurol. Sci. 33 (1–2): 199–206. doi:10.1016/0022-510x(77)90193-9. PMID903782. S2CID32228762.