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首页> 外文期刊>Journal of Electron Microscopy >Ultrastructural transformation of gastric parietal cells reverting from the active to the resting state of acid secretion revealed in isolated rat gastric mucosa model processed by high-pressure freezing
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Ultrastructural transformation of gastric parietal cells reverting from the active to the resting state of acid secretion revealed in isolated rat gastric mucosa model processed by high-pressure freezing

机译:在高压冷冻处理的离体大鼠胃黏膜模型中揭示出胃壁细胞超微结构转变,从活跃的酸分泌状态恢复为静止状态

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To elucidate a functional transformation of gastric parietal cells, we have newly developed an isolated rat gastric mucosa model whose parietal cells exhibited a reverting process from the active to the resting state of acid secretion. Briefly, the parietal cells were treated with cimetidine following prior stimulation of acid secretion in the model, and cryofixed by plunge freezing for light microscopy or high-pressure freezing for electron microscopy. As a result, immunohistochemistry of H+/K+-ATPase demonstrated a progressive translocation of H+/K+-ATPase from the apical to the cytoplasmic region. The ultrastructure of parietal cells at 5 min in the reverting phase was quite similar to that of maximally stimulated one. However, the apical microvilli of intracellular canaliculi (IC) changed bulbous by degrees, resulted in complete occlusion of IC at 60 min in the reverting phase. The apical membranes were subsequently internalized into the cytoplasm forming unique penta-laminar membranes. Interestingly, at 90 min in the reverting phase, the penta-laminar membranes formed a number of multilamellar autophagosomes that were intensely labeled for H+/K+-ATPase. Then, the parietal cells exhibited well-developed Golgi apparatus and lysosomal compartments involving the multilamellar membranes at 105 min, and mostly reverted to their resting conformation at 120 min in the reverting phase. Corresponding to the ultrastructural changes of microvilli, the immunohistochemistry of ezrin showed a dissociation of ezrin from the apical region at 30 min in the reverting phase. The present findings provide new insights into the functional transformation in gastric parietal cells reverting to their resting conformation.
机译:为了阐明胃壁细胞的功能转化,我们新开发了一个分离的大鼠胃粘膜模型,该模型的壁细胞表现出从分泌酸到活性状态的恢复过程。简而言之,先刺激模型中的酸分泌,然后再用西咪替丁处理壁细胞,然后通过急速冷冻进行冷冻固定(用于光学显微镜)或高压冷冻进行冷冻固定(用于电子显微镜)。结果,H + / K + -ATPase的免疫组织化学证明了H + / K + -ATPase。在恢复期的第5分钟,壁细胞的超微结构与最大刺激细胞的超微结构非常相似。然而,细胞内小管(IC)的根尖微绒毛呈球状度改变,导致在恢复期60分钟时IC被完全闭塞。随后将顶膜内化到细胞质中,形成独特的五层膜。有趣的是,在恢复期的90分钟时,五层膜形成了许多多层自噬体,这些吞噬体被强烈标记H + / K + -ATPase。然后,壁细胞在105分钟时表现出发达的高尔基体和涉及多层膜的溶酶体区室,并且在恢复期的120分钟时大部分恢复到其静止构象。对应于微绒毛的超微结构变化,ezrin的免疫组织化学显示在恢复期30分钟时ezrin从根尖区解离。本发现为胃壁细胞恢复其静止构象提供了新的见解。

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