Unmyelinated nerve fibers in the human dental pulp express markers for myelinated fibers and show sodium channel accumulations.
Unmyelinated nerve fibers in the human dental pulp express markers for myelinated fibers and show sodium channel accumulations.
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DOI:
10.1186/1471-2202-13-29
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发表时间:
2012-03-19
期刊:
影响因子:
2.4
通讯作者:
Levinson SR
中科院分区:
文献类型:
--
作者:
Henry MA;Luo S;Levinson SR
The dental pulp is a common source of pain and is used to study peripheral inflammatory pain mechanisms. Results show most fibers are unmyelinated, yet recent findings in experimental animals suggest many pulpal afferents originate from fibers that are myelinated at more proximal locations. Here we use the human dental pulp and confocal microscopy to examine the staining relationships of neurofilament heavy (NFH), a protein commonly expressed in myelinated afferents, with other markers to test the possibility that unmyelinated pulpal afferents originate from myelinated axons. Other staining relationships studied included myelin basic protein (MBP), protein gene product (PGP) 9.5 to identify all nerve fibers, tyrosine hydroxylase (TH) to identify sympathetic fibers, contactin-associated protein (caspr) to identify nodal sites, S-100 to identify Schwann cells and sodium channels (NaChs). Results show NFH expression in most PGP9.5 fibers except those with TH and include the broad expression of NFH in axons lacking MBP. Fibers with NFH and MBP show NaCh clusters at nodal sites as expected, but surprisingly, NaCh accumulations are also seen in unmyelinated fibers with NFH, and in fibers with NFH that lack Schwann cell associations. The expression of NFH in most axons suggests a myelinated origin for many pulpal afferents, while the presence of NaCh clusters in unmyelinated fibers suggests an inherent capacity for the unmyelinated segments of myelinated fibers to form NaCh accumulations. These findings have broad implications on the use of dental pulp to study pain mechanisms and suggest possible novel mechanisms responsible for NaCh cluster formation and neuronal excitability.
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DOI:
10.1023/a:1007053411667
发表时间:
1999-04-01
期刊:
JOURNAL OF NEUROCYTOLOGY
影响因子:
--
作者:
Ching, W;Zanazzi, G;Salzer, JL
通讯作者:
Salzer, JL
影响因子:
3.7
作者:
Bax DA;Little SE;Gaspar N;Perryman L;Marshall L;Viana-Pereira M;Jones TA;Williams RD;Grigoriadis A;Vassal G;Workman P;Sheer D;Reis RM;Pearson AD;Hargrave D;Jones C
通讯作者:
Jones C
影响因子:
2.3
作者:
Hass, Nicole;Schwarzenbacher, Karin;Breer, Heinz
通讯作者:
Breer, Heinz
影响因子:
7.4
作者:
Henry, Michael A.;Freking, Angelique R.;Levinson, S. Rock
通讯作者:
Levinson, S. Rock
影响因子:
16.2
作者:
Eshed, Y;Feinberg, K;Peles, E
通讯作者:
Peles, E