RNA-binding motif
protein 3 is a molecular marker of
hypothermia that has proved neuroprotective in
neurodegenerative disease models. However, its relationship to the well-recognized
therapeutic effect of
hypothermia in
ischaemic stroke had not been studied. In this work, the expression of RNA-binding motif
protein 3 was investigated in ischaemic animal models subjected to systemic and focal brain
hypothermia, specifically the effects of RNA-binding motif
protein 3 silencing and overexpression on ischaemic lesions. Moreover, the association of RNA-binding motif
protein 3 levels with body temperature and clinical outcome was evaluated in two independent cohorts of acute
ischaemic stroke patients (n = 215); these levels were also determined in a third cohort of 31 patients derived from the phase III EuroHYP-1 trial of therapeutic cooling in
ischaemic stroke. The preclinical data confirmed the increase of brain RNA-binding motif
protein 3 levels in ischaemic animals subjected to systemic and focal
hypothermia; this increase was selectively higher in the cooled hemisphere of animals undergoing focal brain
hypothermia, thus confirming the direct effect of
hypothermia on RNA-binding motif
protein 3 expression, while RNA-binding motif
protein 3 up-regulation in ischaemic brain regions led to functional recovery. Clinically, patients with body temperature <37.5°C in the first two cohorts had higher RNA-binding motif
protein 3 values at 24 h and good outcome at 3 months post-
ischaemic stroke, while RNA-binding motif
protein 3 levels in the cooled third cohort tended to exceed those in placebo-treated patients. These results make RNA-binding motif
protein 3 a molecular marker associated with the effect of
hypothermia in
ischaemic stroke and suggest its potential application as a promising protective target.