The current state of knowledge on the role of NKG2D ligands in multiple sclerosis and other autoimmune diseases
Multiple sclerosis (MS) is a chronic central nervous system (CNS) disease with demyelinating inflammatory characteristics. It is the most common nontraumatic and disabling disease affecting young adults. The incidence and prevalence of MS have been increasing. However, its exact cause remains unclea...
Saved in:
Main Authors: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2025-01-01
|
Series: | Frontiers in Molecular Neuroscience |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fnmol.2024.1493308/full |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1841549966413135872 |
---|---|
author | Aleksandra Pogoda-Wesołowska Nina Sługocka Agnieszka Synowiec Klaudia Brodaczewska Marcin Mejer-Zahorowski Maciej Ziękiewicz Wojciech Szypowski Piotr Szymański Adam Stępień |
author_facet | Aleksandra Pogoda-Wesołowska Nina Sługocka Agnieszka Synowiec Klaudia Brodaczewska Marcin Mejer-Zahorowski Maciej Ziękiewicz Wojciech Szypowski Piotr Szymański Adam Stępień |
author_sort | Aleksandra Pogoda-Wesołowska |
collection | DOAJ |
description | Multiple sclerosis (MS) is a chronic central nervous system (CNS) disease with demyelinating inflammatory characteristics. It is the most common nontraumatic and disabling disease affecting young adults. The incidence and prevalence of MS have been increasing. However, its exact cause remains unclear. The main tests used to support the diagnosis are magnetic resonance imaging (MRI) examination and cerebrospinal fluid (CSF) analysis. Nonetheless, to date, no sensitive or specific marker has been identified for the detection of the disease at its initial stage. In recent years, researchers have focused on the fact that the number of natural killer cell group 2 member D (NKG2D) family of C-type lectin-like receptor + (NKG2D+) T cells in the peripheral blood, CSF, and brain tissue has been shown to be higher in patients with MS than in controls. The activating receptor belonging to the NKG2D is stimulated by specific ligands: in humans these are major histocompatibility complex (MHC) class I polypeptide–related sequence A (MICA) and MHC class I polypeptide-related sequence B (MICB) proteins and UL16 binding 1–6 proteins (ULBP1-6). Under physiological conditions, the aforementioned ligands are expressed at low or undetectable levels but can be induced in response to stress factors. NKG2D ligands (NKG2DLs) are involved in epigenetic regulation of their expression. To date, studies in cell cultures, animal models, and brain tissues have revealed elevated expression of MICA/B, ULPB4, and its mouse homolog murine UL16 binding protein-like transcript (MULT1), in oligodendrocytes and astrocytes from patients with MS. Furthermore, soluble forms of NKG2DLs were elevated in the plasma and CSF of patients with MS compared to controls. In this review, we aim to describe the role of NKG2D and NKG2DLs, and their interactions in the pathogenesis of MS, as well as in other autoimmune diseases such as rheumatoid arthritis (RA), inflammatory bowel disease (IBD), systemic lupus erythematosus (SLE), and celiac disease (CeD). We also assess the potential of these proteins as diagnostic markers and consider future perspectives for targeting NKG2D ligands and their pathways as therapeutic targets in MS. |
format | Article |
id | doaj-art-df7192c6b8694b2095942455514bde43 |
institution | Kabale University |
issn | 1662-5099 |
language | English |
publishDate | 2025-01-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Molecular Neuroscience |
spelling | doaj-art-df7192c6b8694b2095942455514bde432025-01-10T11:54:02ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992025-01-011710.3389/fnmol.2024.14933081493308The current state of knowledge on the role of NKG2D ligands in multiple sclerosis and other autoimmune diseasesAleksandra Pogoda-Wesołowska0Nina Sługocka1Agnieszka Synowiec2Klaudia Brodaczewska3Marcin Mejer-Zahorowski4Maciej Ziękiewicz5Wojciech Szypowski6Piotr Szymański7Adam Stępień8Neurology Clinic, Military Institute of Medicine- National Research Institute, Warsaw, PolandFaculty of Medicine, University of Warsaw, Warsaw, PolandLaboratory of Molecular Oncology and Innovative Therapies, Military Institute of Medicine–National Research Institute, Warsaw, PolandLaboratory of Molecular Oncology and Innovative Therapies, Military Institute of Medicine–National Research Institute, Warsaw, PolandNeurology Clinic, Military Institute of Medicine- National Research Institute, Warsaw, PolandNeurology Clinic, Military Institute of Medicine- National Research Institute, Warsaw, PolandNeurology Clinic, Military Institute of Medicine- National Research Institute, Warsaw, PolandNeurology Clinic, Military Institute of Medicine- National Research Institute, Warsaw, PolandNeurology Clinic, Military Institute of Medicine- National Research Institute, Warsaw, PolandMultiple sclerosis (MS) is a chronic central nervous system (CNS) disease with demyelinating inflammatory characteristics. It is the most common nontraumatic and disabling disease affecting young adults. The incidence and prevalence of MS have been increasing. However, its exact cause remains unclear. The main tests used to support the diagnosis are magnetic resonance imaging (MRI) examination and cerebrospinal fluid (CSF) analysis. Nonetheless, to date, no sensitive or specific marker has been identified for the detection of the disease at its initial stage. In recent years, researchers have focused on the fact that the number of natural killer cell group 2 member D (NKG2D) family of C-type lectin-like receptor + (NKG2D+) T cells in the peripheral blood, CSF, and brain tissue has been shown to be higher in patients with MS than in controls. The activating receptor belonging to the NKG2D is stimulated by specific ligands: in humans these are major histocompatibility complex (MHC) class I polypeptide–related sequence A (MICA) and MHC class I polypeptide-related sequence B (MICB) proteins and UL16 binding 1–6 proteins (ULBP1-6). Under physiological conditions, the aforementioned ligands are expressed at low or undetectable levels but can be induced in response to stress factors. NKG2D ligands (NKG2DLs) are involved in epigenetic regulation of their expression. To date, studies in cell cultures, animal models, and brain tissues have revealed elevated expression of MICA/B, ULPB4, and its mouse homolog murine UL16 binding protein-like transcript (MULT1), in oligodendrocytes and astrocytes from patients with MS. Furthermore, soluble forms of NKG2DLs were elevated in the plasma and CSF of patients with MS compared to controls. In this review, we aim to describe the role of NKG2D and NKG2DLs, and their interactions in the pathogenesis of MS, as well as in other autoimmune diseases such as rheumatoid arthritis (RA), inflammatory bowel disease (IBD), systemic lupus erythematosus (SLE), and celiac disease (CeD). We also assess the potential of these proteins as diagnostic markers and consider future perspectives for targeting NKG2D ligands and their pathways as therapeutic targets in MS.https://www.frontiersin.org/articles/10.3389/fnmol.2024.1493308/fullmultiple sclerosisNKG2D ligandsreviewbiomarkersastrocytes |
spellingShingle | Aleksandra Pogoda-Wesołowska Nina Sługocka Agnieszka Synowiec Klaudia Brodaczewska Marcin Mejer-Zahorowski Maciej Ziękiewicz Wojciech Szypowski Piotr Szymański Adam Stępień The current state of knowledge on the role of NKG2D ligands in multiple sclerosis and other autoimmune diseases Frontiers in Molecular Neuroscience multiple sclerosis NKG2D ligands review biomarkers astrocytes |
title | The current state of knowledge on the role of NKG2D ligands in multiple sclerosis and other autoimmune diseases |
title_full | The current state of knowledge on the role of NKG2D ligands in multiple sclerosis and other autoimmune diseases |
title_fullStr | The current state of knowledge on the role of NKG2D ligands in multiple sclerosis and other autoimmune diseases |
title_full_unstemmed | The current state of knowledge on the role of NKG2D ligands in multiple sclerosis and other autoimmune diseases |
title_short | The current state of knowledge on the role of NKG2D ligands in multiple sclerosis and other autoimmune diseases |
title_sort | current state of knowledge on the role of nkg2d ligands in multiple sclerosis and other autoimmune diseases |
topic | multiple sclerosis NKG2D ligands review biomarkers astrocytes |
url | https://www.frontiersin.org/articles/10.3389/fnmol.2024.1493308/full |
work_keys_str_mv | AT aleksandrapogodawesołowska thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT ninasługocka thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT agnieszkasynowiec thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT klaudiabrodaczewska thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT marcinmejerzahorowski thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT maciejziekiewicz thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT wojciechszypowski thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT piotrszymanski thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT adamstepien thecurrentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT aleksandrapogodawesołowska currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT ninasługocka currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT agnieszkasynowiec currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT klaudiabrodaczewska currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT marcinmejerzahorowski currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT maciejziekiewicz currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT wojciechszypowski currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT piotrszymanski currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases AT adamstepien currentstateofknowledgeontheroleofnkg2dligandsinmultiplesclerosisandotherautoimmunediseases |