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Fig. 23.5 Schematic diagram showing the mode of action of taurine in alleviating the apoptosis induced
by ER stress and mitochondrial dysfunction. Taurine can exert its regulation by decreasing GRP78
release, caspase-12 activity, Bax, caspase-3, p-IRE1, ATF6 cleavage, CHOP, and increasing Bcl-2
of both CHOP and caspase-12 by taurine treatment provide substantial evidence
that taurine can contribute to an effective inhibition of ER stress induced by hypoxia/
reoxygenation.
23.5
Conclusion
In summary, as it is shown in Fig. 23.5 , we demonstrated that taurine can exert its
protective effect on CNS neurons both in the in vitro model of hypoxia/reoxygen-
ation and in vivo model of the MCAO through suppression of ER stress. Moreover,
the effect of taurine treatment on the three ER stress-induced signaling pathways
showed that taurine significantly inhibited apoptosis by activation of the ATF6 and
the IRE1 pathway, but not the PERK pathway.
References
Anelli T, Sitia R (2008) Protein quality control in the early secretory pathway. EMBO J
27:315-327
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