Human organ donor-derived vagus nerve biopsies allow for well-preserved ultrastructure and high-resolution mapping of myelinated and unmyelinated fibers.
Human organ donor-derived vagus nerve biopsies allow for well-preserved ultrastructure and high-resolution mapping of myelinated and unmyelinated fibers.
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DOI:
10.1038/s41598-021-03248-1
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发表时间:
2021-12-13
影响因子:
4.6
通讯作者:
Powley TL
中科院分区:
文献类型:
--
作者:
Havton LA;Biscola NP;Stern E;Mihaylov PV;Kubal CA;Wo JM;Gupta A;Baronowsky E;Ward MP;Jaffey DM;Powley TL
The vagus nerve provides motor, sensory, and autonomic innervation of multiple organs, and electrical vagus nerve stimulation (VNS) provides an adjunctive treatment option for e.g. medication-refractory epilepsy and treatment-resistant depression. The mechanisms of action for VNS are not known, and high-resolution anatomical mapping of the human vagus nerve is needed to better understand its functional organization. Electron microscopy (EM) is required for the detection of both myelinated and unmyelinated axons, but access to well-preserved human vagus nerves for ultrastructural studies is sparse. Intact human vagus nerve samples were procured intra-operatively from deceased organ donors, and tissues were immediately immersion fixed and processed for EM. Ultrastructural studies of cervical and sub-diaphragmatic vagus nerve segments showed excellent preservation of the lamellated wall of myelin sheaths, and the axolemma of myelinated and unmyelinated fibers were intact. Microtubules, neurofilaments, and mitochondria were readily identified in the axoplasm, and the ultrastructural integrity of Schwann cell nuclei, Remak bundles, and basal lamina was also well preserved. Digital segmentation of myelinated and unmyelinated axons allowed for determination of fiber size and myelination. We propose a novel source of human vagus nerve tissues for detailed ultrastructural studies and mapping to support efforts to refine neuromodulation strategies, including VNS.
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影响因子:
3.7
作者:
Hammer N;Glätzner J;Feja C;Kühne C;Meixensberger J;Planitzer U;Schleifenbaum S;Tillmann BN;Winkler D
通讯作者:
Winkler D
影响因子:
4.3
作者:
Pelot NA;Goldhagen GB;Cariello JE;Musselman ED;Clissold KA;Ezzell JA;Grill WM
通讯作者:
Grill WM
影响因子:
6.2
作者:
Cao, Yiming;Shahrestani, Sara;Pleass, Henry
通讯作者:
Pleass, Henry
影响因子:
81.5
作者:
Feldman, Eva L.;Callaghan, Brian C.;Viswanathan, Vijay
通讯作者:
Viswanathan, Vijay
影响因子:
--
作者:
HOFFMAN, HH;SCHNITZLEIN, HN
通讯作者:
SCHNITZLEIN, HN