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遗传性脑白质营养不良突变小鼠(震颤小鼠)的周围神经移植

Peripheral nerve grafts in hereditary leukodystrophic mutant mice (twitcher).

作者信息

Scaravilli F, Jacobs J M

出版信息

Nature. 1981 Mar 5;290(5801):56-8. doi: 10.1038/290056a0.

DOI:10.1038/290056a0
PMID:7207584
Abstract

The twitcher mouse is a mutant affected by a form of leukodystrophy which shows close similarities to human globoid cell (Krabbe's) leukodystrophy. Transmission is by an autosomal recessive gene twi. Progressive loss of myelin sheaths from both central and peripheral nervous systems and the presence of inclusion-laden macrophages are characteristic findings. Morphological features of the twitcher have been described by Duchen et al. Nerve iso- and allografting have been used to determine the roles of axon and Schwann cell in a number of mouse and human nerve abnormalities. Schwann cells in a graft proliferate and become associated with regenerating host axons which grow through the graft into the host distal stump. In the twitcher, peripheral nerve axons do not degenerate but are thinner than normal, although there is considerable axonal degeneration in the central nervous system. In 15-day-old mutants, inclusions have been found in Schwann cells associated with apparently normal myelin sheaths. Grafting experiments might show whether the phenotype of this mutant is fully expressed in the Schwann cell, or if axons are also involved. In previous experiments, survival of transplanted Schwann cells was achieved by the use of T cell-suppressed or nude mice. We report here that a twitcher nerve transplanted in immunologically unsuppressed animals reproduces all the characteristic features of leukodystrophy and conversely that Schwann cells from unaffected mice can produce normal myelin when associated with twitcher axons.

摘要

颤抖小鼠是一种受某种形式的脑白质营养不良影响的突变体,它与人类球状细胞(克拉伯氏)脑白质营养不良有密切相似之处。其遗传方式为常染色体隐性基因twi。中枢神经系统和周围神经系统的髓鞘逐渐丧失,以及出现充满包涵体的巨噬细胞是其特征性表现。杜兴等人描述了颤抖小鼠的形态学特征。神经同体移植和异体移植已被用于确定轴突和施万细胞在一些小鼠和人类神经异常中的作用。移植中的施万细胞会增殖,并与再生的宿主轴突相关联,这些轴突通过移植体生长到宿主远端残端。在颤抖小鼠中,周围神经轴突不会退化,但比正常的细,尽管中枢神经系统存在相当程度的轴突变性。在15日龄的突变体中,已在与明显正常的髓鞘相关的施万细胞中发现包涵体。移植实验可能会表明该突变体的表型是否在施万细胞中完全表达,或者轴突是否也参与其中。在之前的实验中,通过使用T细胞抑制的小鼠或裸鼠来实现移植施万细胞的存活。我们在此报告,在免疫未受抑制的动物中移植的颤抖小鼠神经再现了脑白质营养不良的所有特征,相反,来自未受影响小鼠的施万细胞与颤抖小鼠轴突相关联时可产生正常的髓鞘。

相似文献

1
Peripheral nerve grafts in hereditary leukodystrophic mutant mice (twitcher).遗传性脑白质营养不良突变小鼠(震颤小鼠)的周围神经移植
Nature. 1981 Mar 5;290(5801):56-8. doi: 10.1038/290056a0.
2
The pathogenesis of globoid cell leucodystrophy in peripheral nerve of the mouse mutant twitcher.小鼠突变体震颤鼠外周神经中球状细胞脑白质营养不良的发病机制。
J Neurol Sci. 1982 Sep;55(3):285-304. doi: 10.1016/0022-510x(82)90127-7.
3
Peripheral neuropathy in the twitcher mouse: accumulation of extracellular matrix in the endoneurium and aberrant expression of ion channels.颤搐小鼠的周围神经病变:神经内膜中细胞外基质的积累及离子通道的异常表达。
Acta Neuropathol. 2008 May;115(5):577-87. doi: 10.1007/s00401-007-0333-3. Epub 2008 Jan 3.
4
Hereditary leucodystrophy in the mouse: the new mutant twitcher.小鼠遗传性脑白质营养不良:新突变体“抽搐小鼠”
Brain. 1980 Sep;103(3):695-710. doi: 10.1093/brain/103.3.695.
5
Improved myelination in nerve grafts from the leucodystrophic twitcher into trembler mice: evidence for enzyme replacement.白质营养不良的抽搐小鼠神经移植到震颤小鼠中髓鞘形成改善:酶替代的证据。
Brain Res. 1982 Apr 8;237(1):163-72. doi: 10.1016/0006-8993(82)90564-9.
6
Enzyme replacement in grafted nerve of twitcher mouse.对震颤小鼠移植神经进行酶替代治疗。
Nature. 1983;305(5936):713-5. doi: 10.1038/305713a0.
7
The twitcher mouse: attenuated processes of Schwann cells in unmyelinated fibers.抽搐小鼠:无髓纤维中施万细胞的萎缩过程。
Brain Res. 1989 Nov 27;503(1):160-2. doi: 10.1016/0006-8993(89)91719-8.
8
Progressive dysfunction of twitcher Schwann cells is evaluated better in vitro than in vivo.与在体内相比,体外能更好地评估颤搐雪旺细胞的进行性功能障碍。
Brain Res. 1994 Feb 21;637(1-2):106-13. doi: 10.1016/0006-8993(94)91222-x.
9
The twitcher mouse. Central nervous system pathology after bone marrow transplantation.抽搐小鼠。骨髓移植后的中枢神经系统病理学
Lab Invest. 1988 Mar;58(3):302-9.
10
Early axonal loss accompanied by impaired endocytosis, abnormal axonal transport, and decreased microtubule stability occur in the model of Krabbe's disease.在克拉伯病的模型中,早期轴突丢失伴随着内吞作用受损、异常轴突运输和微管稳定性降低。
Neurobiol Dis. 2014 Jun;66:92-103. doi: 10.1016/j.nbd.2014.02.012. Epub 2014 Mar 6.

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Splenic natural killer cell activity in two models of experimental neurodegenerative diseases.两种实验性神经退行性疾病模型中的脾自然杀伤细胞活性。
J Cell Mol Med. 2009 Aug;13(8B):2693-2703. doi: 10.1111/j.1582-4934.2008.00640.x. Epub 2008 Dec 29.
3
Molecular beacon genotyping for globoid cell leukodystrophy from hair roots in the twitcher mouse and rhesus macaque.
利用颤抖小鼠和恒河猴毛发根部进行球状细胞脑白质营养不良的分子信标基因分型
J Neurosci Methods. 2007 Jun 15;163(1):60-6. doi: 10.1016/j.jneumeth.2007.02.019. Epub 2007 Feb 25.
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The twitcher mouse. A model of human globoid cell leukodystrophy (krabbe's disease).抽搐小鼠。人类球状细胞脑白质营养不良(克拉伯病)的模型。
Am J Pathol. 1983 Jun;111(3):394-7.
5
Defective Schwann cell function in canine inherited hypertrophic neuropathy.犬遗传性肥厚性神经病中施万细胞功能缺陷
Acta Neuropathol. 1984;63(1):51-6. doi: 10.1007/BF00688470.
6
Disorders in myelination in the twitcher mutant: immunohistochemical and biochemical studies.震颤突变体髓鞘形成障碍:免疫组织化学和生物化学研究
Neurochem Res. 1985 Aug;10(8):1129-41. doi: 10.1007/BF00965887.