Expression pattern of thymosin beta 4 in the adult human liver

S Nemolato, P Van Eyken, T Cabras, F Cau, Mu Fanari, A Locci, D Fanni, C Gerosa, I Messana, Massimo Castagnola, G. Faa

Risultato della ricerca: Contributo in rivistaArticolo in rivista

17 Citazioni (Scopus)


Thymosin beta-4 (T beta 4) is a member of beta-thymosins, a family of small peptides involved in polymerization of G-actin, and in many critical biological processes including apoptosis, cell migration, angiogenesis, and fibrosis. Previous studies in the newborn liver did not reveal any significant reactivity for T beta 4 during the intrauterine life. The aim of the present study was to investigate by immunohistochemistry T beta 4 expression in the adult normal liver. Thirty-five human liver samples, including 11 needle liver biopsies and 24 liver specimens obtained at autopsy, in which no pathological change was detected at the histological examination, were immunostained utilizing an anti-T beta 4 commercial antibody. T beta 4 was detected in the hepatocytes of all adult normal livers examined. A zonation of T beta 4 expression was evident in the vast majority of cases. Immunostaining was preferentially detected in zone 3, while a minor degree of reactivity was detected in periportal hepatocytes (zone 1). At higher power, T beta 4-reactive granules appeared mainly localized at the biliary pole of hepatocytes. In cases with a strong immunostaining, even perinuclear areas and the sinusoidal pole of hepatocytes appeared interested by immunoreactivity for T beta 4. The current work first evidences a strong diffuse expression of T beta 4 in the adult human liver, and adds hepatocytes to the list of human cells able to synthesize large amounts of T beta 4 in adulthood. Moreover, T beta 4 should be added to the liver proteins characterized by a zonate expression pattern, in a descending gradient from the terminal vein to the periportal areas of the liver acinus. Identifying the intimate role played by this peptide intracellularly and extracellularly, in physiology and in different liver diseases, is a major challenge for future research focusing on T beta 4.
Lingua originaleEnglish
pagine (da-a)131-135
Numero di pagine5
RivistaEuropean Journal of Histochemistry
Stato di pubblicazionePubblicato - 2011




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