Homeostatic regulation of the endoneurial microenvironment during development, aging and in response to trauma, disease and toxic insult.
Homeostatic regulation of the endoneurial microenvironment during development, aging and in response to trauma, disease and toxic insult.
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DOI:
10.1007/s00401-010-0783-x
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发表时间:
2011-03
影响因子:
12.7
通讯作者:
Weerasuriya A
中科院分区:
文献类型:
--
作者:
Mizisin AP;Weerasuriya A
The endoneurial microenvironment, delimited by the endothelium of endoneurial vessels and a multi-layered ensheathing perineurium, is a specialized milieu intérieur within which axons, associated Schwann cells and other resident cells of peripheral nerves function. The endothelium and perineurium restricts as well as regulates exchange of material between the endoneurial microenvironment and the surrounding extracellular space and thus is more appropriately described as a blood–nerve interface (BNI) rather than a blood–nerve barrier (BNB). Input to and output from the endoneurial microenvironment occurs via blood–nerve exchange and convective endoneurial fluid flow driven by a proximo-distal hydrostatic pressure gradient. The independent regulation of the endothelial and perineurial components of the BNI during development, aging and in response to trauma is consistent with homeostatic regulation of the endoneurial microenvironment. Pathophysiological alterations of the endoneurium in experimental allergic neuritis (EAN), and diabetic and lead neuropathy are considered to be perturbations of endoneurial homeostasis. The interactions of Schwann cells, axons, macrophages, and mast cells via cell–cell and cell–matrix signaling regulate the permeability of this interface. A greater knowledge of the dynamic nature of tight junctions and the factors that induce and/or modulate these key elements of the BNI will increase our understanding of peripheral nerve disorders as well as stimulate the development of therapeutic strategies to treat these disorders.
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影响因子:
3.1
作者:
BUNDGAARD, M;FROKJAERJENSEN, J
通讯作者:
FROKJAERJENSEN, J
影响因子:
8.2
作者:
Eaton, RP;Qualls, C;Griffey, RH
通讯作者:
Griffey, RH
影响因子:
14.5
作者:
BROWN, WF;FEASBY, TE
通讯作者:
FEASBY, TE
影响因子:
--
作者:
BURKEL, WE
通讯作者:
BURKEL, WE
DOI:
10.1007/bf00368249
发表时间:
1965-01-01
期刊:
ZEITSCHRIFT FUR ZELLFORSCHUNG UND MIKROSKOPISCHE ANATOMIE
影响因子:
--
作者:
ENERBACK, L;OLSSON, Y;SOURANDER, P
通讯作者:
SOURANDER, P