Blazynski C
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110.
Neurosci Lett. 1991 Jan 2;121(1-2):1-4. doi: 10.1016/0304-3940(91)90634-6.
Uptake of [3H]adenosine and [3H]R-phenylisopropyladenosine (R-PIA) into retinal cells was assessed autoradiographically, in the presence and absence of the purine nucleoside transport inhibitor, nitrobenzylthioinosine (NBI). Under control conditions, both purine nucleosides were accumulated in cell bodies localized to the ganglion cell layer, and the inner nuclear layer. In the presence of NBI, significantly less accumulation of nucleosides within cell bodies was observed, particularly within the inner nuclear layer, suggesting that most of the uptake occurred via the transport of both substrates. The stereoisomer of adenosine, L-[3H]adenosine, was not accumulated into retinal cells consistent with the view that the accumulation of both adenosine and R-PIA occurs via the purine nucleoside transporter.
在存在和不存在嘌呤核苷转运抑制剂硝基苄硫肌苷(NBI)的情况下,通过放射自显影法评估了[3H]腺苷和[3H]R-苯异丙基腺苷(R-PIA)进入视网膜细胞的摄取情况。在对照条件下,两种嘌呤核苷都积聚在位于神经节细胞层和内核层的细胞体中。在存在NBI的情况下,观察到细胞体内核苷的积聚明显减少,尤其是在内核层内,这表明大部分摄取是通过两种底物的转运发生的。腺苷的立体异构体L-[3H]腺苷没有积聚到视网膜细胞中,这与腺苷和R-PIA的积聚都是通过嘌呤核苷转运体发生的观点一致。