GRP78

Grp78
  • 文章类型: Journal Article
    背景:新冠肺炎感染于2020年3月11日被世卫组织宣布为全球大流行。已知GRP78蛋白参与多种病毒的入侵。我们目前的研究试图为新冠肺炎患者GRP78蛋白水平的变化提供一些见解,Covid-19(+)肺炎,与正常人群相比,CT阴性的Covid-19感染病例更多。
    方法:42例Covid-19(-)肺炎患者;72例Covid-19感染患者(30例肺炎,42例CT阴性患者)和30例无已知疾病的患者(对照组)在临床和放射学评估后纳入研究。通过市售的酶联免疫吸附测定(ELISA)试剂盒测量受试者的血清GRP78水平。
    结果:发现新冠肺炎感染组的GRP78水平显著高于新冠肺炎(-)肺炎组和对照组(分别为p=0.031和p=0.0001)。Covid-19(-)肺炎之间没有显着差异,就GRP78水平而言,Covid-19(+)肺炎和CT阴性Covid19感染组(p=0.09)。此外,Covid-19(-)肺炎组的GRP78水平显著高于对照组(p=0.0001).
    结论:这项前瞻性病例对照研究表明,与新冠肺炎和对照组相比,新冠肺炎感染期间血清GRP78水平显著升高。随着SARS-CoV-2病毒与GRP78蛋白之间的联系越来越清楚,这种关联可能会成为治疗目标。
    BACKGROUND: Covid-19 infection was declared a global pandemic by WHO on March 11, 2020. GRP78 protein is known to be involved in the intrusion of numerous viruses. Our current study tries to provide some insight into the variation of GRP78 protein levels in patients with Covid-19 (-) pneumonia, Covid-19 (+) pneumonia, and CT negative Covid-19 infection in comparison to the normal population through a larger number of cases.
    METHODS: 42 patients who have Covid-19 (-) pneumonia; 72 patients who have Covid-19 infection (30 pneumonia,42 CT negative patients) and 30 patient who have no known diseases (control group) have included in the study after the clinical and radiological evaluation. Serum GRP78 levels of the subjects were measured through a commercially available enzyme-linked immunosorbent assay (ELISA) kit.
    RESULTS: The GRP78 level was found to be significantly higher in the Covid-19 infection group than both Covid-19 (-) pneumonia and control group (p = 0.031 and p = 0.0001, respectively).No significant difference was evident between Covid-19 (-) pneumonia, Covid-19 (+) pneumonia and CT negative Covid 19 infection groups with respect to GRP78 levels (p = 0.09). In addition, the GRP78 levels were significantly higher in the Covid-19 (-) pneumonia group than the control group (p = 0.0001).
    CONCLUSIONS: This prospective case-control study reveals that the serum GRP78 levels significantly increased during Covid-19 infection in comparison to both the Covid-19 (-) pneumonia and the control group. As the association between SARS-CoV-2 virus and GRP78 protein is revealed more clearly, this association may come to the fore as a therapeutic target.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

       PDF(Pubmed)

  • 文章类型: Comparative Study
    目的:一种新型人类冠状病毒,命名为SARS-COV-2,最近在世界各地造成数千人死亡。内质网应激在疾病的发生发展中起着重要作用。
    方法:我们旨在研究SARS-COV-2感染患者与肺炎患者的ER应激标志物之间的关系。共有9例患者(4例诊断为肺炎,5例诊断为SARS-COV-2感染)因肺炎和SARS-COV-2症状入院。纳入18名无任何已知慢性或急性疾病和药物使用的健康个体作为健康对照组。血清人葡萄糖调节蛋白78(GRP78),采用酶联免疫吸附试验(ELISA)检测血清人C/EBP同源蛋白(CHOP)和血清人磷酸化细胞外信号调节激酶(PERK)水平。
    结果:发现与其他组的个体相比,SARS-COV-2阳性病例中的GRP78水平明显更高。与其他组相比,SARS-COV-2阳性组的血清GRP-78水平中位数在统计学上明显更高(p=0.0003)。SARS-COV-2阳性肺炎病例的血清PERK水平在统计学上显着升高(p=0.046)。
    结论:显示GRP78与SARS-COV-2感染之间存在关联。尽管对少数患者进行了调查,这些结果将对SARS-COV-2的未来治疗具有重要意义。
    OBJECTIVE: A novel human coronavirus, named SARS-COV-2, has recently caused thousands of deaths all around the world. Endoplasmic reticulum (ER) stress plays an important role in the development of diseases.
    METHODS: We aimed to to investigate the relationship between ER stress markers in patients infected with SARS-COV-2 and patients with pneumonia. A total of 9 patients (4 patients diagnosed with pneumonia and 5 patients diagnosed with SARS-COV-2 infection) who admitted to the emergency Department with symptoms of pneumonia and SARS-COV-2 were included in the study. A total of 18 healthy individuals without any known chronic or acute disease and drug use were included as the healthy control group. Serum human glucose regulated protein 78 (GRP78), serum human C/EBP homologous protein (CHOP) and serum human phospho extracellular signal regulated kinase (PERK) levels were measured using enzyme-linked immunosorbent assay (ELISA).
    RESULTS: GRP78 levels were found to be significantly higher in SARS-COV-2 positive cases compared to individuals in other groups. Serum GRP-78 level median value was statistically significantly higher in SARS-COV-2-positive group compared to the other groups (p=0.0003). Serum PERK level was statistically significantly higher in SARS-COV-2-positive pneumonia cases (p=0.046).
    CONCLUSIONS: An association was shown between GRP78 and SARS-COV-2 infection. Although a small number of patients was investigated, these results will be important and guide future treatments of SARS-COV-2.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

       PDF(Pubmed)

  • 文章类型: Journal Article
    OBJECTIVE: The purpose of this study was to determine the value of the endoplasmic reticulum (ER) stress markers glucose-regulated protein 78 (GRP78), C/EBP homologous protein (CHOP) and PERK in predicting the success of cardiopulmonary resuscitation (CPR) or post-CPR survival.
    METHODS: Non-traumatic out-of-hospital CA patients were included in this prospective, nested case-control study. Standard CPR and post-resuscitative care were applied. Levels of ER stress markers were measured at presentation and were investigated to determine whether they might constitute a marker predicting return of spontaneous circulation (ROSC) or sustained ROSC, and of 24-h, and 1 and 3-month survival.
    RESULTS: Fifty-two out of 99 non-traumatic CA patients were enrolled. ROSC was determined at a level of 25%, sustained ROSC at 23%, 24-h survival at 7%, and 1- and 3-month survival at 4.6%. No difference was determined in terms of ER stress markers between patients with and without ROSC or sustained ROSC. Only PERK levels were higher in surviving patients than non-surviving subjects in terms of 24-h survival (p = 0.01). Otherwise, no stress markers differed between surviving and non-surviving patients at any survival time point.
    CONCLUSIONS: ER stress markers are of no value in determining establishment of ROSC or sustained ROSC, success of CPR, or survival. Only PERK levels may be valuable in terms of 24-h survival.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

       PDF(Pubmed)

  • 文章类型: Case Reports
    暂无摘要。
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

公众号