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碳酸酐酶 II、IX 和 XII 与反流性食管炎。

Carbonic Anhydrases II, IX, and XII in Reflux Esophagitis.

机构信息

Cancer and Translational Medicine Research Unit, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, 90014, Oulu, Finland.

Anesthesia and Intensive Care, Research Unit of Surgery, University of Oulu, Oulu, Finland.

出版信息

Dig Dis Sci. 2022 May;67(5):1761-1772. doi: 10.1007/s10620-021-06985-5. Epub 2021 Apr 30.

Abstract

BACKGROUND

The pathogenesis of gastroesophageal reflux disease (GERD) has not been resolved in detail. Esophageal epithelial cells provide resistance to acidic reflux via several mechanisms, many of which involve buffering acid with bicarbonate and transporting protons. Carbonic anhydrases (CAs) are enzymes that control the acid-base balance by catalyzing the reversible hydration of carbon dioxide to produce bicarbonate and hydrogen ions.

AIMS

We aimed to determine the immunohistochemical expression patterns of CAII, CAIX, and CAXII in the normal esophageal squamous epithelium and in patients with GERD.

METHODS

We evaluated 82 biopsy samples, including 26 with a histologically normal esophagus, 26 with histologically mild esophagitis, and 30 with severe esophagitis. Expression patterns of CAII, CAIX, and CAXII in the esophageal squamous epithelium were determined by immunohistochemical staining.

RESULTS

Cytoplasmic CAII expression was predominantly detected in the upper luminal part of the squamous epithelium and was significantly (p < 0.01) increased in GERD. Expression of CAIX was essentially membranous. The isozyme was constantly present in the peripapillary cells. In the interpapillary areas, clustered expression was observed to emerge and increase significantly (p < 0.01) in esophagitis. CAXII expression was the most abundant of the isozymes and was mainly membranous. In the normal squamous epithelium, CAXII expression was confined to the basal layer; in severe esophagitis, CAXII expression increased significantly in both basal (p < 0.05) and superficial (p < 0.01) halves of the epithelium.

CONCLUSIONS

We demonstrate upregulated expression of CAII, CAIX, and CAXII in GERD. The increase in expression likely contributes to esophageal epithelial resistance to acidic reflux.

摘要

背景

胃食管反流病(GERD)的发病机制尚未得到详细阐明。食管上皮细胞通过多种机制提供对酸性反流的抵抗力,其中许多机制涉及用碳酸氢盐缓冲酸并转运质子。碳酸酐酶(CA)是通过催化二氧化碳的可逆水合反应生成碳酸氢盐和氢离子来控制酸碱平衡的酶。

目的

我们旨在确定 CAII、CAIX 和 CAXII 在正常食管鳞状上皮和 GERD 患者中的免疫组织化学表达模式。

方法

我们评估了 82 个活检样本,包括 26 个具有组织学正常食管、26 个具有组织学轻度食管炎和 30 个具有严重食管炎的样本。通过免疫组织化学染色确定食管鳞状上皮中 CAII、CAIX 和 CAXII 的表达模式。

结果

细胞质 CAII 表达主要在上皮腔的上部检测到,在 GERD 中显著增加(p<0.01)。CAIX 的表达基本上是膜性的。同工酶在乳头周围细胞中持续存在。在乳头间区域,观察到簇状表达,并在食管炎中显著增加(p<0.01)。CAXII 表达是同工酶中最丰富的,主要是膜性的。在正常鳞状上皮中,CAXII 表达局限于基底层;在严重食管炎中,CAXII 表达在上皮的基底(p<0.05)和浅层(p<0.01)均显著增加。

结论

我们证明了 GERD 中 CAII、CAIX 和 CAXII 的表达上调。表达的增加可能有助于食管上皮抵抗酸性反流。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/699f/9142434/744acbc3753d/10620_2021_6985_Fig1_HTML.jpg

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