MMP-9 expression is increased in B lymphocytes during multiple sclerosis exacerbation and is regulated by microRNA-320a.

MMP-9 expression is increased in B lymphocytes during multiple sclerosis exacerbation and is regulated by microRNA-320a.
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DOI:
10.1016/j.jneuroim.2014.11.004
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发表时间:
2015-01-15
影响因子:
3.3
通讯作者:
Balashov, Konstantin E.
Balashov, Konstantin E.
中科院分区:
医学4区
文献类型:
--
作者:
Aung, Latt Latt;Mouradian, M. Maral;Dhib-Jalbut, Suhayl;Balashov, Konstantin E.

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B细胞是维持复发性多发性硬化症(MS)的疾病活动所必需的,并产生破坏血脑屏障的基质金属肽酶-9(MMP-9)。与缓解期相比,在疾病复发期间MS患者的B淋巴细胞中,MMP-9蛋白表达增加,靶向MMP-9 mRNA的microRNA-320 a(miR-320 a)表达显著降低。通过用miR-320 a抑制剂转染人B淋巴细胞,从而导致MMP-9表达和分泌增加,证实了这些发现的功能意义。总之,MS患者的B细胞中miR-320 a的表达降低,可能导致血脑屏障通透性增加和神经功能障碍。
B cells are necessary to maintain disease activity in relapsing multiple sclerosis (MS) and produce matrix metallopeptidase-9 (MMP-9), which disrupts the blood-brain barrier. MMP-9 protein expression was increased and expression of microRNA-320a (miR-320a), which targets MMP-9 mRNA, was significantly decreased in B lymphocytes of MS patients during a disease relapse compared to remission. Functional significance of these findings was demonstrated by transfecting human B lymphocytes with miR-320a inhibitor, which led to increased MMP-9 expression and secretion. In summary, expression of miR-320a is decreased in B cells of MS patients and may contribute to increased blood-brain barrier permeability and neurological disability.
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影响因子: 5.8
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