## Abstract The extracellular matrix glycoprotein tenascin‐R (TN‐R) has been implicated in a variety of cell‐matrix interactions involved in the molecular control of axon guidance and neural cell migration during development and regeneration of the central nervous system (CNS). Whereas TN‐R is ampl
Expression of protein 4.1G in Schwann cells of the peripheral nervous system
✍ Scribed by Nobuhiko Ohno; Nobuo Terada; Hisashi Yamakawa; Masayuki Komada; Osamu Ohara; Bruce D. Trapp; Shinichi Ohno
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 998 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
The membrane‐associated cytoskeletal proteins, including protein 4.1 family, play important roles in membrane integrity, protein targeting, and signal transduction. Although protein 4.1G (4.1G) is expressed ubiquitously in mammalian tissues, it can have very discrete distributions within cells. The present study investigated the expression and distributions of 4.1G in rodent sciatic nerve. Northern and Western blot analysis detected abundant 4.1G mRNA and protein in rat sciatic nerve extracts. Immunohistochemical staining with a 4.1G‐specific antibody and double immunolabeling with E‐cadherin, βIV spectrin, and connexin 32 detected 4.1G in paranodal loops, Schmidt‐Lanterman incisures, and periaxonal, mesaxonal, and abaxonal membranes of rodent sciatic nerve. Immunoelectron microscopy confirmed the immunodistribution of 4.1G in Schwann cells. In developing mouse sciatic nerves, 4.1G was diffusely distributed in immature Schwann cells and gradually localized at paranodes, incisures, and periaxonal and mesaxonal membranes during their maturation. These data support the concept that 4.1G plays an important role in the membrane expansion and specialization that occurs during formation and maintenance of myelin internodes in the peripheral nervous system. © 2006 Wiley‐Liss, Inc.
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