Bashan N, Gahl W A, Tietze F, Bernardini I, Schulman J D
Biochim Biophys Acta. 1984 Nov 7;777(2):267-73. doi: 10.1016/0005-2736(84)90429-2.
This paper describes the stimulation of exodus of cystine from lysosome-rich granular fractions by potassium. Potassium permeability into lysosomes is low, but in the presence of an ionophore or permeable anion, the movement of K+ into lysosomes caused a large stimulation of cystine exodus. Lysosomal preparations from leucocytes of cystinotic patients, which lack carrier-mediated cystine transport, also manifested stimulation of cystine egress by valinomycin and K+. This suggests that potassium-dependent cystine egress involves a carrier different from that defective in cystinosis, or occurs through a non-carrier-mediated mechanism.
本文描述了钾对富含溶酶体的颗粒组分中胱氨酸外流的刺激作用。钾进入溶酶体的通透性较低,但在离子载体或可渗透阴离子存在的情况下,钾离子进入溶酶体的运动导致胱氨酸外流受到极大刺激。来自胱氨酸病患者白细胞的溶酶体制剂缺乏载体介导的胱氨酸转运,缬氨霉素和钾也能刺激其胱氨酸外流。这表明钾依赖性胱氨酸外流涉及一种不同于胱氨酸病中缺陷的载体,或者是通过非载体介导的机制发生的。