The role of heat shock proteins (HSPs) in type 2 diabetes mellitus pathophysiology
Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by sustained hyperglycemia caused by impaired insulin signaling and secretion. Metabolic stress, caused by an inappropriate diet, is one of the major hallmarks provoking inflammation, endoplasmic reticulum (ER) stress, and mitocho...
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Published in | Journal of diabetes and its complications Vol. 37; no. 11; p. 108564 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.11.2023
Elsevier Limited |
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Abstract | Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by sustained hyperglycemia caused by impaired insulin signaling and secretion. Metabolic stress, caused by an inappropriate diet, is one of the major hallmarks provoking inflammation, endoplasmic reticulum (ER) stress, and mitochondrial dysfunction. Heat shock proteins (HSPs) are a group of highly conserved proteins that have a crucial role in chaperoning damaged and misfolded proteins to avoid disruption of cellular homeostasis under stress conditions. To do this, HSPs interact with diverse intra-and extracellular pathways among which are the insulin signaling, insulin secretion, and apoptosis pathways. Therefore, HSP dysfunction, e.g. HSP70, may lead to disruption of the pathways responsible for insulin secretion and uptake. Consistently, the altered expression of other HSPs and genetic polymorphisms in HSP-producing genes in diabetic subjects has made HSPs hot research in T2DM. This paper provides a comprehensive overview of the role of different HSPs in T2DM pathogenesis, affected cellular pathways, and the potential therapeutic strategies targeting HSPs in T2DM.
•The altered expression of HSPs in T2DM holds great potential to investigate their role in disease pathogenesis and their applicability as a target in clinical approaches. |
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AbstractList | Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by sustained hyperglycemia caused by impaired insulin signaling and secretion. Metabolic stress, caused by an inappropriate diet, is one of the major hallmarks provoking inflammation, endoplasmic reticulum (ER) stress, and mitochondrial dysfunction. Heat shock proteins (HSPs) are a group of highly conserved proteins that have a crucial role in chaperoning damaged and misfolded proteins to avoid disruption of cellular homeostasis under stress conditions. To do this, HSPs interact with diverse intra-and extracellular pathways among which are the insulin signaling, insulin secretion, and apoptosis pathways. Therefore, HSP dysfunction, e.g. HSP70, may lead to disruption of the pathways responsible for insulin secretion and uptake. Consistently, the altered expression of other HSPs and genetic polymorphisms in HSP-producing genes in diabetic subjects has made HSPs hot research in T2DM. This paper provides a comprehensive overview of the role of different HSPs in T2DM pathogenesis, affected cellular pathways, and the potential therapeutic strategies targeting HSPs in T2DM. Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by sustained hyperglycemia caused by impaired insulin signaling and secretion. Metabolic stress, caused by an inappropriate diet, is one of the major hallmarks provoking inflammation, endoplasmic reticulum (ER) stress, and mitochondrial dysfunction. Heat shock proteins (HSPs) are a group of highly conserved proteins that have a crucial role in chaperoning damaged and misfolded proteins to avoid disruption of cellular homeostasis under stress conditions. To do this, HSPs interact with diverse intra-and extracellular pathways among which are the insulin signaling, insulin secretion, and apoptosis pathways. Therefore, HSP dysfunction, e.g. HSP70, may lead to disruption of the pathways responsible for insulin secretion and uptake. Consistently, the altered expression of other HSPs and genetic polymorphisms in HSP-producing genes in diabetic subjects has made HSPs hot research in T2DM. This paper provides a comprehensive overview of the role of different HSPs in T2DM pathogenesis, affected cellular pathways, and the potential therapeutic strategies targeting HSPs in T2DM. •The altered expression of HSPs in T2DM holds great potential to investigate their role in disease pathogenesis and their applicability as a target in clinical approaches. Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by sustained hyperglycemia caused by impaired insulin signaling and secretion. Metabolic stress, caused by an inappropriate diet, is one of the major hallmarks provoking inflammation, endoplasmic reticulum (ER) stress, and mitochondrial dysfunction. Heat shock proteins (HSPs) are a group of highly conserved proteins that have a crucial role in chaperoning damaged and misfolded proteins to avoid disruption of cellular homeostasis under stress conditions. To do this, HSPs interact with diverse intra-and extracellular pathways among which are the insulin signaling, insulin secretion, and apoptosis pathways. Therefore, HSP dysfunction, e.g. HSP70, may lead to disruption of the pathways responsible for insulin secretion and uptake. Consistently, the altered expression of other HSPs and genetic polymorphisms in HSP-producing genes in diabetic subjects has made HSPs hot research in T2DM. This paper provides a comprehensive overview of the role of different HSPs in T2DM pathogenesis, affected cellular pathways, and the potential therapeutic strategies targeting HSPs in T2DM.Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by sustained hyperglycemia caused by impaired insulin signaling and secretion. Metabolic stress, caused by an inappropriate diet, is one of the major hallmarks provoking inflammation, endoplasmic reticulum (ER) stress, and mitochondrial dysfunction. Heat shock proteins (HSPs) are a group of highly conserved proteins that have a crucial role in chaperoning damaged and misfolded proteins to avoid disruption of cellular homeostasis under stress conditions. To do this, HSPs interact with diverse intra-and extracellular pathways among which are the insulin signaling, insulin secretion, and apoptosis pathways. Therefore, HSP dysfunction, e.g. HSP70, may lead to disruption of the pathways responsible for insulin secretion and uptake. Consistently, the altered expression of other HSPs and genetic polymorphisms in HSP-producing genes in diabetic subjects has made HSPs hot research in T2DM. This paper provides a comprehensive overview of the role of different HSPs in T2DM pathogenesis, affected cellular pathways, and the potential therapeutic strategies targeting HSPs in T2DM. |
ArticleNumber | 108564 |
Author | Elahi, Reza Rezakhani, Negin Esmaeilzadeh, Abdolreza Mohammadi, Vahid |
Author_xml | – sequence: 1 givenname: Abdolreza surname: Esmaeilzadeh fullname: Esmaeilzadeh, Abdolreza email: A46reza@zums.ac.ir organization: Department of Immunology, Zanjan University of Medical Sciences, Zanjan, Iran – sequence: 2 givenname: Vahid surname: Mohammadi fullname: Mohammadi, Vahid organization: School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran – sequence: 3 givenname: Reza surname: Elahi fullname: Elahi, Reza organization: School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran – sequence: 4 givenname: Negin surname: Rezakhani fullname: Rezakhani, Negin organization: School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37852076$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_molimm_2024_03_009 crossref_primary_10_1007_s12015_023_10668_1 crossref_primary_10_1186_s40538_024_00726_2 crossref_primary_10_1002_pca_3477 |
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Keywords | HSP70 Type 2 diabetes mellitus Insulin Heat shock protein |
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Snippet | Type 2 diabetes mellitus (T2DM) is a metabolic disorder characterized by sustained hyperglycemia caused by impaired insulin signaling and secretion. Metabolic... |
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SubjectTerms | Apoptosis Cytokines Diabetes Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - genetics Diabetes Mellitus, Type 2 - metabolism Genes Heat shock protein Heat shock proteins Heat-Shock Proteins - genetics Heat-Shock Proteins - metabolism Homeostasis HSP70 HSP70 Heat-Shock Proteins - genetics HSP70 Heat-Shock Proteins - metabolism Humans Hyperglycemia Insulin Insulin resistance Kinases Metabolism Molecular Chaperones Musculoskeletal system Pathogenesis Pathophysiology Phosphorylation Physiology Stress Transcription factors Type 2 diabetes mellitus |
Title | The role of heat shock proteins (HSPs) in type 2 diabetes mellitus pathophysiology |
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