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人唾液腺中β-防御素基因的表达

Expression of beta-defensin genes by human salivary glands.

作者信息

Bonass W A, High A S, Owen P J, Devine D A

机构信息

Leeds Dental Institute, University of Leeds, United Kingdom.

出版信息

Oral Microbiol Immunol. 1999 Dec;14(6):371-4. doi: 10.1034/j.1399-302x.1999.140607.x.

Abstract

This study investigated expression of genes encoding human beta-defensins 1 and 2 by human salivary glands. Tissues from surgical biopsies were collected fresh onto ice and stored in liquid nitrogen. Total RNA was extracted using Trizol reagent and human beta-defensin messenger RNA detected by reverse transcriptase polymerase chain reaction amplification. DNA sequencing of amplified fragments, after ligation into pGEM-T Easy vector and transformation of competent Escherichia coli, confirmed identities of cloned fragments. Human beta-defensin 1 messenger RNA was detected in all 25 samples that generated amplifiable cDNA, as assessed using abl-specific primers. Three of 13 submandibular gland samples (two normal, one chronically inflamed), and 2 of 2 minor salivary gland samples (one normal, one chronically inflamed) expressed human beta-defensin 2 messenger RNA. All six parotid gland samples studied were negative for human beta-defensin 2 messenger RNA. Thus, human beta-defensin 1 gene expression occurred in all human major and minor salivary glands studied, whereas human beta-defensin 2 expression occurred only in a small number of gland samples.

摘要

本研究调查了人类唾液腺中编码人β-防御素1和2的基因表达情况。手术活检组织新鲜采集于冰上,并储存于液氮中。使用Trizol试剂提取总RNA,并通过逆转录聚合酶链反应扩增检测人β-防御素信使RNA。将扩增片段连接到pGEM-T Easy载体并转化感受态大肠杆菌后,对扩增片段进行DNA测序,确认了克隆片段的身份。使用abl特异性引物评估,在所有25个产生可扩增cDNA的样本中均检测到了人β-防御素1信使RNA。13个下颌下腺样本中的3个(2个正常,1个慢性炎症)以及2个小唾液腺样本中的2个(1个正常,1个慢性炎症)表达了人β-防御素2信使RNA。研究的所有6个腮腺样本中人β-防御素2信使RNA均为阴性。因此,在所研究的所有人类大、小唾液腺中均发生了人β-防御素1基因表达,而人β-防御素2仅在少数腺体样本中表达。

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