Laminins and their receptors in Schwann cells and hereditary neuropathies

被引:76
作者
Feltri, ML [1 ]
Wrabetz, L [1 ]
机构
[1] Ist Sci San Raffaele, DIBIT 4A2, I-20132 Milan, Italy
关键词
congenital muscular dystrophy; dystroglycan; integrin; laminin; mice; myelin; node of Ranvier; radial sorting; Schwann cell; targeted mutagenesis;
D O I
10.1111/j.1085-9489.2005.0010204.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This review focuses on the influence of laminins, mediated through laminin receptors present on Schwann cells, on peripheral nerve development and pathology. Laminins influence multiple aspects of cell differentiation and tissue morphogenesis, including cell survival, proliferation, cytoskeletal rearrangements, and polarity. Peripheral nerves are no exception, as shown by the discovery that defective laminin signals contribute to the pathogenesis of diverse neuropathies such as merosin-deficient congenital muscular dystrophy and Charcot-Marie-Tooth 4F, neurofibromatosis, and leprosy. In the last 5 years, advanced molecular and cell biological techniques and conditional mutagenesis in mice began revealing the role of different laminins and receptors in developing nerves. In this way, we are starting to explain morphological and pathological observations beginning at the start of the last century. Here, we review these recent advances and show how the roles of laminins and their receptors are surprisingly varied in both time and place.
引用
收藏
页码:128 / 143
页数:16
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