Heat shock protein and antioxidant enzyme gene expression and fold changes in bone marrow samples from healthy rats

Walaa Mustafa, A. S. Alchalabi
{"title":"Heat shock protein and antioxidant enzyme gene expression and fold changes in bone marrow samples from healthy rats","authors":"Walaa Mustafa, A. S. Alchalabi","doi":"10.33899/edusj.2022.134710.1260","DOIUrl":null,"url":null,"abstract":"The hematopoiesis in the bone marrow in the early stages of life is very complex and involves many cellular factors under very strict micro-environments. The two important cellular factors are heat shock proteins and antioxidant enzymes. The aim of the study was to study the gene expression profile of healthy rats’ bone marrow cells and niches particularly heat shock proteins and antioxidant genes. A total of thirty healthy Wister Albino rats at one, two, and three months old were involved throughout the study. Bone marrow samples were collected at a specified date according to the study design and utilized for qPCR test for expression of Hsps27, 90α, 90β, and antioxidant enzymes glutathione peroxidase1 (GPX1), catalase CAT and superoxide dismutase (SOD3) genes. The results revealed that there was a clear expression of both Hsps90α andβ in bone marrow cells throughout the study as well as the GPX1 gene. Furthermore, there was an increase in fold change of Hsps90α and β as well as GPX1, CAT, and SOD3 proteins as age progressed. In conclusion, hematopoietic cell differentiation and proliferation are regulated by bone marrow microenvironment stress conditions and by the expression of different Hsps and antioxidant genes. The protein folding process is a defense mechanism to protect the HSCs, and progenitors from un/misfolded proteins and to keep proteostasis.","PeriodicalId":33491,"journal":{"name":"mjl@ ltrby@ wl`lm","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"mjl@ ltrby@ wl`lm","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33899/edusj.2022.134710.1260","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The hematopoiesis in the bone marrow in the early stages of life is very complex and involves many cellular factors under very strict micro-environments. The two important cellular factors are heat shock proteins and antioxidant enzymes. The aim of the study was to study the gene expression profile of healthy rats’ bone marrow cells and niches particularly heat shock proteins and antioxidant genes. A total of thirty healthy Wister Albino rats at one, two, and three months old were involved throughout the study. Bone marrow samples were collected at a specified date according to the study design and utilized for qPCR test for expression of Hsps27, 90α, 90β, and antioxidant enzymes glutathione peroxidase1 (GPX1), catalase CAT and superoxide dismutase (SOD3) genes. The results revealed that there was a clear expression of both Hsps90α andβ in bone marrow cells throughout the study as well as the GPX1 gene. Furthermore, there was an increase in fold change of Hsps90α and β as well as GPX1, CAT, and SOD3 proteins as age progressed. In conclusion, hematopoietic cell differentiation and proliferation are regulated by bone marrow microenvironment stress conditions and by the expression of different Hsps and antioxidant genes. The protein folding process is a defense mechanism to protect the HSCs, and progenitors from un/misfolded proteins and to keep proteostasis.
健康大鼠骨髓样品热休克蛋白和抗氧化酶基因表达及折叠变化
在生命的早期阶段,骨髓中的造血是非常复杂的,并且在非常严格的微观环境下涉及许多细胞因素。两个重要的细胞因子是热休克蛋白和抗氧化酶。本研究的目的是研究健康大鼠骨髓细胞的基因表达谱和小生境,特别是热休克蛋白和抗氧化基因。在整个研究中,共有30只1、2和3个月大的健康Wister Albino大鼠参与。根据研究设计,在指定日期采集骨髓样本,并用于qPCR检测Hsps27、90α、90β和抗氧化酶谷胱甘肽过氧化物酶1(GPX1)、过氧化氢酶CAT和超氧化物歧化酶(SOD3)基因的表达。结果显示,在整个研究过程中,Hsps90α和β在骨髓细胞中以及GPX1基因中都有明确的表达。此外,随着年龄的增长,Hsps90α和β以及GPX1、CAT和SOD3蛋白的倍数变化增加。总之,造血细胞的分化和增殖受骨髓微环境应激条件以及不同Hsps和抗氧化基因的表达的调节。蛋白质折叠过程是一种保护HSC和祖细胞免受未折叠/错误折叠蛋白质影响并保持蛋白稳定的防御机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
38
审稿时长
24 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信