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

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 ju...

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Veröffentlicht in:Journal of comparative neurology (1911) 2004-07, Vol.474 (4), p.578-588
Hauptverfasser: Roux, Kyle J., Amici, Stephanie A., Notterpek, Lucia
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creator Roux, Kyle J.
Amici, Stephanie A.
Notterpek, Lucia
description 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.
doi_str_mv 10.1002/cne.20154
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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. 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Comp. Neurol</addtitle><description>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. 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Comp. Neurol</addtitle><date>2004-07-05</date><risdate>2004</risdate><volume>474</volume><issue>4</issue><spage>578</spage><epage>588</epage><pages>578-588</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><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. 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subjects adherens junctions
Animals
Animals, Newborn
Blood-Brain Barrier - embryology
Blood-Brain Barrier - physiology
Blotting, Northern
Brain - blood supply
Brain - embryology
Brain - physiology
brain endothelial
Cells, Cultured
Embryo, Mammalian
Endothelial Cells - metabolism
gas3
Immunohistochemistry
Intercellular Junctions - physiology
Myelin Proteins - biosynthesis
neuroepithelial
Rats
Sciatic Nerve - blood supply
Sciatic Nerve - embryology
Sciatic Nerve - physiology
tight junctions
tight junctions, neuroepithelial
title The temporospatial expression of peripheral myelin protein 22 at the developing blood-nerve and blood-brain barriers
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