Cardelli-Cangiano P, Fiori A, Cangiano C, Barberini F, Allegra P, Peresempio V, Strom R
Dipartimenti di Biopatologia Umana e di Scienze Biochimiche, Università di Roma La Sapienza, Italy.
J Neurochem. 1987 Dec;49(6):1667-75. doi: 10.1111/j.1471-4159.1987.tb02424.x.
On treatment with collagenase, brain microvessels, together with several protein components, lose some enzymatic activities such as alkaline phosphatase and gamma-glutamyltranspeptidase, whereas no change occurs in the activities of 5'-nucleotidase and glutamine synthetase. The energy-requiring "A-system" of polar neutral amino acid transport is also severely inactivated, whereas the L-system for the facilitated exchange of branched chain and aromatic amino acids is preserved. In the collagenase-digested microvessels, this leads to loss of the transtimulation effect of glutamine on the transport of large neutral amino acids, because such transtimulation is due to a cooperation between the A- and L-systems. By contrast, NH4+ maintains (and even enhances) its ability to stimulate the L-system of amino acid transport, presumably through glutamine synthesis within the endothelial cells.
用胶原酶处理后,脑微血管连同几种蛋白质成分会丧失一些酶活性,如碱性磷酸酶和γ-谷氨酰转肽酶,而5'-核苷酸酶和谷氨酰胺合成酶的活性则没有变化。极性中性氨基酸转运的需能“A系统”也会严重失活,而促进支链和芳香族氨基酸交换的L系统则得以保留。在经胶原酶消化的微血管中,这导致谷氨酰胺对大中性氨基酸转运的转刺激作用丧失,因为这种转刺激是由于A系统和L系统之间的协同作用。相比之下,NH4+维持(甚至增强)其刺激氨基酸转运L系统的能力,推测是通过内皮细胞内的谷氨酰胺合成来实现的。