Expression of human B-Cell specific receptor FCRL1 in healthy individuals and in patients with autoimmune diseases
The expression levels of the FCRL1 gene, which encodes a human B-cell surface receptor, were compared in healthy individuals and patients with autoimmune diseases. The expression levels were evaluated using DNA dot hybridization on membranes with spotted cDNA samples derived from blood-cell sub-popu...
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Published in | Molecular biology (New York) Vol. 46; no. 3; pp. 450 - 456 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Dordrecht
SP MAIK Nauka/Interperiodica
01.05.2012
Springer Nature B.V |
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Abstract | The expression levels of the
FCRL1
gene, which encodes a human B-cell surface receptor, were compared in healthy individuals and patients with autoimmune diseases. The expression levels were evaluated using DNA dot hybridization on membranes with spotted cDNA samples derived from blood-cell sub-populations of patients with autoimmune diseases. Quantification of the hybridization signals showed that
FCRL1
expression in peripheral blood B-lymphocytes of patients with multiple sclerosis, lupus anticoagulants, Takayasu’s arteritis, and von Willebrand disease was significantly higher than in healthy individuals. Monoclonal and polyclonal FCRL1-specific antibodies that enable FCRL1 detection in Western blotting, immunohistochemistry, and flow-cytometry assays were generated. It was found that FCRL1 is expressed on the surfaces of mature CD19+ B-cells. In the tonsils, FCRL1-positive cells were located in the crypt area, i.e., in the mantle zone of secondary lymphoid follicles and among the cells of lymphoid epithelium. FCRL1-positive cells were also found in B-cell follicles of the spleen. |
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AbstractList | The expression levels of the
FCRL1
gene, which encodes a human B-cell surface receptor, were compared in healthy individuals and patients with autoimmune diseases. The expression levels were evaluated using DNA dot hybridization on membranes with spotted cDNA samples derived from blood-cell sub-populations of patients with autoimmune diseases. Quantification of the hybridization signals showed that
FCRL1
expression in peripheral blood B-lymphocytes of patients with multiple sclerosis, lupus anticoagulants, Takayasu’s arteritis, and von Willebrand disease was significantly higher than in healthy individuals. Monoclonal and polyclonal FCRL1-specific antibodies that enable FCRL1 detection in Western blotting, immunohistochemistry, and flow-cytometry assays were generated. It was found that FCRL1 is expressed on the surfaces of mature CD19+ B-cells. In the tonsils, FCRL1-positive cells were located in the crypt area, i.e., in the mantle zone of secondary lymphoid follicles and among the cells of lymphoid epithelium. FCRL1-positive cells were also found in B-cell follicles of the spleen. The expression levels of the FCRL1 gene, which encodes a human B-cell surface receptor, were compared in healthy individuals and patients with autoimmune diseases. The expression levels were evaluated using DNA dot hybridization on membranes with spotted cDNA samples derived from blood-cell sub-populations of patients with autoimmune diseases. Quantification of the hybridization signals showed that FCRL1 expression in peripheral blood B-lymphocytes of patients with multiple sclerosis, lupus anticoagulants, Takayasu's arteritis, and von Willebrand disease was significantly higher than in healthy individuals. Monoclonal and polyclonal FCRL1-specific antibodies that enable FCRL1 detection in Western blotting, immunohistochemistry, and flow-cytometry assays were generated. It was found that FCRL1 is expressed on the surfaces of mature CD19+ B-cells. In the tonsils, FCRL1-positive cells were located in the crypt area, i.e., in the mantle zone of secondary lymphoid follicles and among the cells of lymphoid epithelium. FCRL1-positive cells were also found in B-cell follicles of the spleen. The expression levels of the FCRL1 gene, which encodes a human B-cell surface receptor, were compared in healthy individuals and patients with autoimmune diseases. The expression levels were evaluated using DNA dot hybridization on membranes with spotted cDNA samples derived from blood-cell sub-populations of patients with autoimmune diseases. Quantification of the hybridization signals showed that FCRL1 expression in peripheral blood B-lymphocytes of patients with multiple sclerosis, lupus anticoagulants, Takayasu's arteritis, and von Willebrand disease was significantly higher than in healthy individuals. Monoclonal and polyclonal FCRL1-specific antibodies that enable FCRL1 detection in Western blotting, immunohistochemistry, and flow-cytometry assays were generated. It was found that FCRL1 is expressed on the surfaces of mature CD19+ B-cells. In the tonsils, FCRL1-positive cells were located in the crypt area, i.e., in the mantle zone of secondary lymphoid follicles and among the cells of lymphoid epithelium. FCRL1-positive cells were also found in B-cell follicles of the spleen.[PUBLICATION ABSTRACT] |
Author | Mechetina, L. V. Nikulina, G. M. Taranin, A. V. Chikaev, N. A. Reshetnikova, E. S. Volkova, O. Yu Baranov, K. O. Najakshin, A. M. |
Author_xml | – sequence: 1 givenname: K. O. surname: Baranov fullname: Baranov, K. O. email: baranov@mcb.nsc.ru organization: Department of Molecular and Cell Biology, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences – sequence: 2 givenname: O. Yu surname: Volkova fullname: Volkova, O. Yu organization: Department of Molecular and Cell Biology, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences – sequence: 3 givenname: L. V. surname: Mechetina fullname: Mechetina, L. V. organization: Department of Molecular and Cell Biology, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences – sequence: 4 givenname: N. A. surname: Chikaev fullname: Chikaev, N. A. organization: Department of Molecular and Cell Biology, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences – sequence: 5 givenname: E. S. surname: Reshetnikova fullname: Reshetnikova, E. S. organization: Department of Molecular and Cell Biology, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences – sequence: 6 givenname: G. M. surname: Nikulina fullname: Nikulina, G. M. organization: Central Clinical Hospital, Siberian Branch, Russian Academy of Sciences – sequence: 7 givenname: A. V. surname: Taranin fullname: Taranin, A. V. organization: Department of Molecular and Cell Biology, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences – sequence: 8 givenname: A. M. surname: Najakshin fullname: Najakshin, A. M. organization: Department of Molecular and Cell Biology, Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences |
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CitedBy_id | crossref_primary_10_1080_14728222_2018_1472768 crossref_primary_10_1016_j_humimm_2021_01_011 crossref_primary_10_1128_jvi_01760_22 crossref_primary_10_1038_s41598_019_54612_1 crossref_primary_10_1038_s41598_020_74035_7 crossref_primary_10_1007_s00296_016_3495_2 crossref_primary_10_1007_s11033_022_08104_7 crossref_primary_10_1177_1177271919882351 |
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Keywords | autoimmune diseases flow cytometry B cells FCRL family immunohistochemistry monoclonal antibody |
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Snippet | The expression levels of the
FCRL1
gene, which encodes a human B-cell surface receptor, were compared in healthy individuals and patients with autoimmune... The expression levels of the FCRL1 gene, which encodes a human B-cell surface receptor, were compared in healthy individuals and patients with autoimmune... |
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SubjectTerms | Antibodies Autoimmune diseases Biochemistry Biomedical and Life Sciences Cellular biology Deoxyribonucleic acid DNA Flow cytometry Gene expression Human Genetics Immunohistochemistry Life Sciences Molecular Biomedicine Special Issue Monoclonal antibodies |
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Title | Expression of human B-Cell specific receptor FCRL1 in healthy individuals and in patients with autoimmune diseases |
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