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Immunology. 1992 May;76(1):133-9.

本文引用的文献

1
Use of isolated brain capillaries and cultured endothelial cells to study the blood-brain barrier.使用分离的脑毛细血管和培养的内皮细胞来研究血脑屏障。
Fed Proc. 1984 Feb;43(2):191-5.
2
Identification and quantitation of T lymphocyte subsets found in the spinal cord of the Lewis rat during acute experimental allergic encephalomyelitis.急性实验性变应性脑脊髓炎期间Lewis大鼠脊髓中T淋巴细胞亚群的鉴定与定量分析。
J Immunol. 1983 Dec;131(6):2805-9.
3
The immunopathology of experimental allergic encephalomyelitis. II. Endothelial cell Ia increases prior to inflammatory cell infiltration.实验性变应性脑脊髓炎的免疫病理学。II. 炎症细胞浸润之前内皮细胞Ia增加。
J Immunol. 1984 May;132(5):2402-7.
4
Ia expression by vascular endothelium is inducible by activated T cells and by human gamma interferon.血管内皮细胞的Ia表达可被活化的T细胞和人γ干扰素诱导。
J Exp Med. 1983 Apr 1;157(4):1339-53. doi: 10.1084/jem.157.4.1339.
5
The mechanism of antigen presentation by endothelial cells.
Immunobiology. 1984 Dec;168(3-5):453-69. doi: 10.1016/S0171-2985(84)80130-8.
6
Ultracytochemical distribution of myelin basic protein after injection into the cerebrospinal fluid. Evidence for transport through the blood-brain barrier and binding to the luminal surface of cerebral veins.注射入脑脊液后髓鞘碱性蛋白的超细胞化学分布。通过血脑屏障转运并结合至脑静脉腔面的证据。
J Neurol Sci. 1984 Mar;63(3):423-33. doi: 10.1016/0022-510x(84)90165-5.
7
Mouse monoclonal antibodies against rat major histocompatibility antigens. Two Ia antigens and expression of Ia and class I antigens in rat thymus.抗大鼠主要组织相容性抗原的小鼠单克隆抗体。两种Ia抗原以及Ia和I类抗原在大鼠胸腺中的表达。
Eur J Immunol. 1982 Mar;12(3):237-43. doi: 10.1002/eji.1830120313.
8
The endothelium--astrocyte immune control system of the brain.大脑的内皮细胞-星形胶质细胞免疫控制系统。
Springer Semin Immunopathol. 1985;8(1-2):57-70. doi: 10.1007/BF00197247.
9
On the presence of Ia-positive endothelial cells and astrocytes in multiple sclerosis lesions and its relevance to antigen presentation.多发性硬化症病灶中Ia阳性内皮细胞和星形胶质细胞的存在及其与抗原呈递的相关性。
J Neuroimmunol. 1985 Apr;8(1):1-14. doi: 10.1016/s0165-5728(85)80043-6.
10
Ia antigens in the normal rat nervous system and in lesions of experimental allergic encephalomyelitis.正常大鼠神经系统及实验性变态反应性脑脊髓炎病变中的Ia抗原
Acta Neuropathol. 1985;68(4):263-72. doi: 10.1007/BF00690828.

脑内皮细胞中MHC基因表达及mRNA合成的动力学

Kinetics of MHC gene expression and mRNA synthesis in brain endothelium.

作者信息

Male D, Pryce G

机构信息

Department of Neuropathology, Institute of Psychiatry, London, U.K.

出版信息

Immunology. 1988 Jan;63(1):37-42.

PMID:3123371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1454708/
Abstract

Rat brain endothelium was examined in vitro to determine the sequence of events in MHC gene activation following IFN-gamma stimulation. The cell-triggering time, kinetics of mRNA synthesis, rate of MHC induction and rate of decay were measured by quantifying cell-surface MHC expression in the presence or absence of alpha-amanitin. Enhanced class I expression is triggered immediately after IFN-gamma stimulation, and is maximally induced by 4 hr of stimulation. New class I mRNA synthesis starts immediately and proceeds over the next 24 hr. This is followed by increased expression of class I molecules, which reaches plateau levels by 24 hr. While IFN-gamma is present, enhanced class I expression is maintained at 140-200% of that seen on resting cells. On removal of IFN-gamma, class I expression decays towards the levels seen on resting cells, with a half-life of approximately 40 hr. Class II molecules can be induced on these cells as well, but it requires the continuous presence of higher levels of IFN-gamma for more than 48 hr to trigger the cells. Induced class II molecules start to appear 2 days after pulsing and continue to increase until Day 4. If the IFN-gamma is removed from the cultures, class II expression declines rapidly towards zero, with a half-life of approximately 30 hr.

摘要

对大鼠脑内皮细胞进行体外研究,以确定γ干扰素刺激后MHC基因激活过程中的事件顺序。通过在有或无α-鹅膏蕈碱存在的情况下定量细胞表面MHC表达,来测量细胞触发时间、mRNA合成动力学、MHC诱导率和衰减率。I类表达在γ干扰素刺激后立即增强,刺激4小时后达到最大诱导水平。新的I类mRNA合成立即开始,并在接下来的24小时内持续进行。随后I类分子表达增加,到24小时达到平台期。在γ干扰素存在的情况下,I类表达维持在静息细胞的140%-200%。去除γ干扰素后,I类表达向静息细胞水平衰减,半衰期约为40小时。这些细胞上也可诱导II类分子,但需要持续存在更高水平的γ干扰素超过48小时才能触发细胞。诱导的II类分子在脉冲后2天开始出现,并持续增加直至第4天。如果从培养物中去除γ干扰素,II类表达迅速下降至零,半衰期约为30小时。