Cell Differentiation and Proliferation in the Bone Marrow and Other Organs of 2D2 Mice during Spontaneous Development of EAE Leading to the Production of Abzymes

The exact cellular and molecular mechanisms of multiple sclerosis and other autoimmune diseases have not been established. Autoimmune pathologies are known to be associated with faults in the immune system and changes in the differentiation profiles of bone marrow stem cells. This study analyzed var...

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Main Authors: Kseniya S. Aulova, Andrey E. Urusov, Ludmila B. Toporkova, Sergey E. Sedykh, Juliya A. Shevchenko, Valeriy P. Tereshchenko, Sergei V. Sennikov, Irina A. Orlovskaya, Georgy A. Nevinsky
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Molecules
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Online Access:https://www.mdpi.com/1420-3049/27/7/2195
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author Kseniya S. Aulova
Andrey E. Urusov
Ludmila B. Toporkova
Sergey E. Sedykh
Juliya A. Shevchenko
Valeriy P. Tereshchenko
Sergei V. Sennikov
Irina A. Orlovskaya
Georgy A. Nevinsky
author_facet Kseniya S. Aulova
Andrey E. Urusov
Ludmila B. Toporkova
Sergey E. Sedykh
Juliya A. Shevchenko
Valeriy P. Tereshchenko
Sergei V. Sennikov
Irina A. Orlovskaya
Georgy A. Nevinsky
author_sort Kseniya S. Aulova
collection DOAJ
description The exact cellular and molecular mechanisms of multiple sclerosis and other autoimmune diseases have not been established. Autoimmune pathologies are known to be associated with faults in the immune system and changes in the differentiation profiles of bone marrow stem cells. This study analyzed various characteristics of experimental autoimmune encephalomyelitis (EAE) in 2D2 mice. Differentiation profiles of six hematopoietic stem cells of bone marrow were found to significantly differ in 2D2 male and female mice during the spontaneous development of EAE. In addition, we found various properties of B and T cells, CD4+ and CD8+ lymphocytes in blood and several organs (bone marrow, spleen, thymus, and lymph nodes) of 2D2 male and female mice to be considerably different. These changes in hematopoietic stem cells differentiation profiles and level of lymphocyte proliferation in various organs of 2D2 mice were found to induce the production of IgGs against DNA, myelin basic protein, and myelin oligodendrocyte glycoprotein, increasing the number of autoantibodies hydrolyzing these substrates. We compared the changes of these immunological and biochemical parameters in 2D2 mice with those of mice of two other lines (Th and C57BL/6), also prone to spontaneous development of EAE. Some noticeable and even extreme variations were found in the time-related development of parameters between male and female mice of 2D2, Th, and C57BL/6 lines. Despite some differences, mice of all three lines demonstrated the changes in hematopoietic stem cells profiles, lymphocyte content, and production of catalytic autoantibodies. Given that these changes are harmful to mice, we believe them to cause the development of experimental autoimmune encephalomyelitis.
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spelling doaj.art-2fb2245551c14782a4427ad85a5f6c812023-11-30T23:40:53ZengMDPI AGMolecules1420-30492022-03-01277219510.3390/molecules27072195Cell Differentiation and Proliferation in the Bone Marrow and Other Organs of 2D2 Mice during Spontaneous Development of EAE Leading to the Production of AbzymesKseniya S. Aulova0Andrey E. Urusov1Ludmila B. Toporkova2Sergey E. Sedykh3Juliya A. Shevchenko4Valeriy P. Tereshchenko5Sergei V. Sennikov6Irina A. Orlovskaya7Georgy A. Nevinsky8Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaInstitute of Clinical Immunology, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaInstitute of Clinical Immunology, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaInstitute of Clinical Immunology, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaInstitute of Clinical Immunology, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaInstitute of Clinical Immunology, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, RussiaThe exact cellular and molecular mechanisms of multiple sclerosis and other autoimmune diseases have not been established. Autoimmune pathologies are known to be associated with faults in the immune system and changes in the differentiation profiles of bone marrow stem cells. This study analyzed various characteristics of experimental autoimmune encephalomyelitis (EAE) in 2D2 mice. Differentiation profiles of six hematopoietic stem cells of bone marrow were found to significantly differ in 2D2 male and female mice during the spontaneous development of EAE. In addition, we found various properties of B and T cells, CD4+ and CD8+ lymphocytes in blood and several organs (bone marrow, spleen, thymus, and lymph nodes) of 2D2 male and female mice to be considerably different. These changes in hematopoietic stem cells differentiation profiles and level of lymphocyte proliferation in various organs of 2D2 mice were found to induce the production of IgGs against DNA, myelin basic protein, and myelin oligodendrocyte glycoprotein, increasing the number of autoantibodies hydrolyzing these substrates. We compared the changes of these immunological and biochemical parameters in 2D2 mice with those of mice of two other lines (Th and C57BL/6), also prone to spontaneous development of EAE. Some noticeable and even extreme variations were found in the time-related development of parameters between male and female mice of 2D2, Th, and C57BL/6 lines. Despite some differences, mice of all three lines demonstrated the changes in hematopoietic stem cells profiles, lymphocyte content, and production of catalytic autoantibodies. Given that these changes are harmful to mice, we believe them to cause the development of experimental autoimmune encephalomyelitis.https://www.mdpi.com/1420-3049/27/7/21952D2Th and C57BL/6 EAE micedevelopment of experimental autoimmune encephalomyelitis (EAE)hematopoietic stem cells differentiationlymphocyte proliferation in different organscatalytic antibodies
spellingShingle Kseniya S. Aulova
Andrey E. Urusov
Ludmila B. Toporkova
Sergey E. Sedykh
Juliya A. Shevchenko
Valeriy P. Tereshchenko
Sergei V. Sennikov
Irina A. Orlovskaya
Georgy A. Nevinsky
Cell Differentiation and Proliferation in the Bone Marrow and Other Organs of 2D2 Mice during Spontaneous Development of EAE Leading to the Production of Abzymes
Molecules
2D2
Th and C57BL/6 EAE mice
development of experimental autoimmune encephalomyelitis (EAE)
hematopoietic stem cells differentiation
lymphocyte proliferation in different organs
catalytic antibodies
title Cell Differentiation and Proliferation in the Bone Marrow and Other Organs of 2D2 Mice during Spontaneous Development of EAE Leading to the Production of Abzymes
title_full Cell Differentiation and Proliferation in the Bone Marrow and Other Organs of 2D2 Mice during Spontaneous Development of EAE Leading to the Production of Abzymes
title_fullStr Cell Differentiation and Proliferation in the Bone Marrow and Other Organs of 2D2 Mice during Spontaneous Development of EAE Leading to the Production of Abzymes
title_full_unstemmed Cell Differentiation and Proliferation in the Bone Marrow and Other Organs of 2D2 Mice during Spontaneous Development of EAE Leading to the Production of Abzymes
title_short Cell Differentiation and Proliferation in the Bone Marrow and Other Organs of 2D2 Mice during Spontaneous Development of EAE Leading to the Production of Abzymes
title_sort cell differentiation and proliferation in the bone marrow and other organs of 2d2 mice during spontaneous development of eae leading to the production of abzymes
topic 2D2
Th and C57BL/6 EAE mice
development of experimental autoimmune encephalomyelitis (EAE)
hematopoietic stem cells differentiation
lymphocyte proliferation in different organs
catalytic antibodies
url https://www.mdpi.com/1420-3049/27/7/2195
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