Enders R H, Judd R M, Donohue T M, Smith C H
Am J Physiol. 1976 Mar;230(3):706-10. doi: 10.1152/ajplegacy.1976.230.3.706.
The human placenta is known to concentrate nearly all amino acids intracellularly for transfer to the fetus. To clarify the mechanism and regulation of this process we have determined the specificity of the principal placental transport systems for neutral amino acids. With the use of competitive inhibition techniques, three transport systems of overlapping specificity have been elucidated. These correspond approximately to the "A", "L", and "ASC" systems of Christensen and associates. In the placenta the specificity of these systems is as follows: A system - alpha aminoisobutyric acid (AIB), glycine, proline, N-methylalanine, alanine, serine, threonine, and glutamine; L system - isoleucine, valine, phenylalanine, BCH, alanine, serine, threonine, and glutamine; and ASC system - alanine, serine, threonine, and glutamine. Placental AIB uptake previously has been shown to increase with preincubation of tissue in vitro. This increase has now been found to be limited to the A system. Activity of the other two systems is essentially unaffected, demonstrating that the transport pathways are separately regulated.
已知人类胎盘会在细胞内浓缩几乎所有氨基酸,以便将其转运给胎儿。为了阐明这一过程的机制和调节方式,我们确定了胎盘主要中性氨基酸转运系统的特异性。通过使用竞争性抑制技术,已阐明了三种特异性重叠的转运系统。这些系统大致对应于克里斯滕森及其同事提出的“A”“L”和“ASC”系统。在胎盘中,这些系统的特异性如下:A系统——α-氨基异丁酸(AIB)、甘氨酸、脯氨酸、N-甲基丙氨酸、丙氨酸、丝氨酸、苏氨酸和谷氨酰胺;L系统——异亮氨酸、缬氨酸、苯丙氨酸、BCH、丙氨酸、丝氨酸、苏氨酸和谷氨酰胺;以及ASC系统——丙氨酸、丝氨酸、苏氨酸和谷氨酰胺。先前已表明,胎盘对AIB的摄取会随着体外组织预孵育而增加。现在发现这种增加仅限于A系统。其他两个系统的活性基本不受影响,这表明转运途径是分别调节的。