Cited by 27

The temporospatial expression of peripheral myelin protein 22 at the developing blood‐nerve and blood‐brain barriers

Roux, Kyle J., Amici, Stephanie A., Notterpek, Lucia·2004·Journal of Comparative Neurology

Abstract

Peripheral myelin protein 22 (PMP22), also known as growth arrest‐specific gene 3 (gas3), is a tetraspan membrane protein whose misexpression is associated with demyelinating peripheral neuropathies. Although the function of PMP22 in Schwann cells is unknown, the protein is found at intercellular junctions of various epithelia and endothelia. To begin to elucidate the role of PMP22 at cell junctions, we examined the temporal expression and protein localization during development and maturation of the rat blood‐nerve barrier (BNB) and blood‐brain barrier (BBB). Developing and adult rat sciatic nerves and brains were coimmunostained for PMP22 and known junctional proteins including zonula occludens‐1 (ZO‐1), occludin, and claudin‐5. Prior to the maturation of the BNB and BBB and detection of the tight junction protein occludin, PMP22 is present at ZO‐1 positive endothelial junctions of the sciatic nerve and brain cortex. The subcellular localization of PMP22 in cultured brain endothelia was confirmed by internalization with ZO‐1 after EGTA‐induced disruption of cell junctions. In choroid epithelia, PMP22 is detected along with occludin and ZO‐1 as early as embryonic day 15 (E15). In agreement, PMP22 message is elevated in P1 rat brain microvasculature and choroid epithelia, compared with total cortex. Additionally, neuroepithelial cell junctions in the embryonic rat brain are immunoreactive for PMP22, ZO‐1, and β‐catenin but not occludin. Together, these studies identify PMP22 as an early constituent of intercellular junctions in the developing and mature rat BNB and BBB. J. Comp. Neurol. 474:578–588, 2004. © 2004 Wiley‐Liss, Inc.

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Crossref · 10.1002/cne.20154

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Authors
Roux, K. J., Amici, S. A., & Notterpek, L.
Venue
Journal of Comparative Neurology
Publisher
Wiley
Published
2004-05-27
Volume
474
Issue
4
Pages
578-588
ISSN
  • 0021-9967
  • 1096-9861
Cited by
27
References
4
Language
en

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