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血清和糖皮质激素调节激酶-1 在乳糜泻患儿十二指肠黏膜中的表达增加。

Increased expression of serum- and glucocorticoid-regulated kinase-1 in the duodenal mucosa of children with coeliac disease.

机构信息

Research Group for Pediatrics and Nephrology, Semmelweis University and Hungarian Academy of Sciences, Bókay J. u. 53-54, Budapest, Hungary.

出版信息

J Pediatr Gastroenterol Nutr. 2010 Feb;50(2):147-53. doi: 10.1097/MPG.0b013e3181b47608.

Abstract

OBJECTIVES

Enterocyte apoptosis induced by activated intraepithelial lymphocytes is increased in coeliac disease (CD). Serum- and glucocorticoid-regulated kinase-1 (SGK1) is a serine/threonine protein kinase that may inhibit apoptosis and compensate for the excessive death of surface epithelial cells. The significance of SGK1 in CD is elusive so far. The aim of this study was to characterise the expression and localisation of SGK1 in duodenal biopsy samples taken from children with untreated CD, children with treated CD, and controls.

PATIENTS AND METHODS

Duodenal biopsy specimens were collected from 16 children with untreated CD, 9 children with treated CD, and 10 controls. The mRNA expression of SGK1 was determined by real-time reverse transcription-polymerase chain reaction. SGK1 and phosphorylated (P)-SGK1 protein levels and their localisation were determined by Western blot and immunofluorescent staining, respectively.

RESULTS

We found increased SGK1-mRNA expression as well as higher SGK1 and P-SGK1 protein levels in the duodenal mucosa of children with untreated CD compared with controls. In the duodenal mucosa of children with treated CD, SGK1-mRNA expression was decreased and SGK1 and P-SGK1 protein levels were lower than in untreated CD. SGK1 and P-SGK1 staining intensity was stronger in duodenal villous enterocytes of children with untreated CD compared with treated CD.

CONCLUSIONS

Our results of increased expression of SGK1 in untreated CD may suggest its contribution to the enterocyte survival in this disease.

摘要

目的

在乳糜泻(CD)中,活化的上皮内淋巴细胞诱导的肠上皮细胞凋亡增加。血清和糖皮质激素调节激酶-1(SGK1)是一种丝氨酸/苏氨酸蛋白激酶,可抑制细胞凋亡并补偿表面上皮细胞的过度死亡。迄今为止,SGK1 在 CD 中的意义尚不清楚。本研究旨在描述未经治疗的 CD 患儿、治疗后的 CD 患儿和对照组十二指肠活检样本中 SGK1 的表达和定位。

患者和方法

收集 16 例未经治疗的 CD 患儿、9 例治疗后的 CD 患儿和 10 例对照组的十二指肠活检标本。通过实时逆转录-聚合酶链反应确定 SGK1 的 mRNA 表达。通过 Western blot 和免疫荧光染色分别确定 SGK1 和磷酸化(P)-SGK1 蛋白水平及其定位。

结果

与对照组相比,未经治疗的 CD 患儿十二指肠黏膜中 SGK1-mRNA 表达增加,SGK1 和 P-SGK1 蛋白水平升高。在治疗后的 CD 患儿的十二指肠黏膜中,SGK1-mRNA 表达降低,SGK1 和 P-SGK1 蛋白水平低于未经治疗的 CD。未经治疗的 CD 患儿的十二指肠绒毛肠上皮细胞中 SGK1 和 P-SGK1 染色强度强于治疗后的 CD。

结论

我们在未经治疗的 CD 中发现 SGK1 表达增加的结果可能表明其有助于该疾病中肠上皮细胞的存活。

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