Increased Expression of Ubiquitin-Specific Protease 4 Participates in Neuronal Apoptosis After Intracerebral Hemorrhage in Adult Rats

• DOI: 10.1007/s10571-016-0375-y
• Publication Date: 2016-04-25T11:24:44Z
• Authors: Chao Liu; Chun Liu; Hanzhang Liu; Leilei Gong; Tao Tao; Yifen Shen; Shunxing Zhu; Aiguo Shen
• Keywords: Male; Neurons; 0301 basic medicine; Aging; Ubiquitin-Protein Ligases; Fluorescent Antibody Technique; Apoptosis; Rats, Sprague-Dawley; 03 medical and health sciences; Phenotype; Animals; Ubiquitin-Specific Proteases; Biomarkers; Cerebral Hemorrhage

Ubiquitinating enzymes catalyze protein ubiquitination, a reversible process countered by deubiquitinating enzyme (DUB) action. Ubiquitin-specific protease 4 (USP4) is a member of the ubiquitin-specific protease (USP) family of DUBs that has a role in spliceosome regulation. In the present study, we demonstrated that USP4 may be involved in neuronal apoptosis in the processes of intracerebral hemorrhage (ICH). We obtained a significant up-regulation of USP4 in neurons adjacent to the hematoma following ICH by the results of Western blot, immunohistochemistry, and immunofluorescence. Increasing USP4 level was found to be accompanied by the up-regulation of active caspase-3, γH2AX, Bax, and decreased expression of Bcl-2. In addition, USP4 co-localized well with γH2AX in the nucleus in the ICH model and hemin-induced apoptosis model. Moreover, in vitro study, knocking down USP4 by USP4-specific siRNA in PC12 cells reduced active caspase-3 expression. All these results above suggested that USP4 may be involved in neuronal apoptosis after ICH.