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与肥大细胞相关的肌内 Cajal 间质细胞在贲门失弛缓症中能在含氮能神经中存活。

Intramuscular interstitial cells of Cajal associated with mast cells survive nitrergic nerves in achalasia.

作者信息

Zarate N, Wang X Y, Tougas G, Anvari M, Birch D, Mearin F, Malagelada J-R, Huizinga J D

机构信息

IDRP, McMaster University, ON, Canada.

出版信息

Neurogastroenterol Motil. 2006 Jul;18(7):556-68. doi: 10.1111/j.1365-2982.2006.00788.x.

DOI:10.1111/j.1365-2982.2006.00788.x
PMID:16771771
Abstract

Achalasia is dominated by injury to inhibitory nerves. As intramuscular interstitial cells of Cajal (ICC-IM) are proposed to form functional units with nitrergic nerves, their fate in achalasia may be critically important. We studied the relationship between loss of nitrergic nerves and injury to ICC-IM in patients with achalasia and determined associations between ICC-IM and mast cells (MC), using quantitative immunohistochemistry and electron microscopy. Loss of neuronal nitric oxide synthase (nNOS) immunoreactivity was completed within 3 years of acquiring achalasia. Thereafter, progressive ultrastructural injury to remaining nerve structures was evident. Within the first 2 years, the number of ICC-IM did not decline although ultrastructural injury was already present. Thereafter, loss of ICC-IM occurred unrelated to duration of disease. Damage to ICC-IM appeared unrelated to nerve injury. A significant MC infiltration was observed in the musculature; the number of MC was positively related to the persistent number of ICC-IM. Mast cell formed close contacts with ICC-IM and piecemeal-degranulation occurred towards ICC-IM. In conclusion, injury to ICC-IM in achalasia is variable, but not related to duration of disease and injury to nitrergic nerves. MC are prominent and form close functional contact with ICC-IM which may be responsible for their relatively long survival.

摘要

贲门失弛缓症主要由抑制性神经损伤引起。由于肌间 Cajal 间质细胞(ICC-IM)被认为与含氮神经形成功能单位,它们在贲门失弛缓症中的命运可能至关重要。我们使用定量免疫组织化学和电子显微镜研究了贲门失弛缓症患者中含氮神经丧失与 ICC-IM 损伤之间的关系,并确定了 ICC-IM 与肥大细胞(MC)之间的关联。神经元型一氧化氮合酶(nNOS)免疫反应性的丧失在患贲门失弛缓症的 3 年内完成。此后,剩余神经结构出现进行性超微结构损伤。在最初的 2 年内,尽管已经存在超微结构损伤,但 ICC-IM 的数量并未下降。此后,ICC-IM 的丧失与疾病持续时间无关。ICC-IM 的损伤似乎与神经损伤无关。在肌肉组织中观察到明显的 MC 浸润;MC 的数量与 ICC-IM 的持续数量呈正相关。肥大细胞与 ICC-IM 形成紧密接触,并向 ICC-IM 发生颗粒逐片释放。总之,贲门失弛缓症中 ICC-IM 的损伤是可变的,但与疾病持续时间和含氮神经损伤无关。MC 很突出,并与 ICC-IM 形成紧密的功能接触,这可能是它们相对长期存活的原因。

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