Peripheral blood T cells and monocytes and B cell lines derived from patients with lupus express estrogen receptor transcripts similar to those of normal cells
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作者:
Suenaga, R
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机构:St Lukes Hosp, Immunol Res Lab, Ctr Rheumat Dis, Kansas City, MO 64111 USA
Suenaga, R
Evans, MJ
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机构:St Lukes Hosp, Immunol Res Lab, Ctr Rheumat Dis, Kansas City, MO 64111 USA
Evans, MJ
Mitamura, K
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机构:St Lukes Hosp, Immunol Res Lab, Ctr Rheumat Dis, Kansas City, MO 64111 USA
Mitamura, K
Rider, V
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机构:St Lukes Hosp, Immunol Res Lab, Ctr Rheumat Dis, Kansas City, MO 64111 USA
Rider, V
Abdou, NI
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机构:St Lukes Hosp, Immunol Res Lab, Ctr Rheumat Dis, Kansas City, MO 64111 USA
Abdou, NI
机构:
[1] St Lukes Hosp, Immunol Res Lab, Ctr Rheumat Dis, Kansas City, MO 64111 USA
[2] Univ Missouri, Sch Biol Sci, Kansas City, MO 64110 USA
[3] St Lukes Hosp, Ctr Allergy & Immunol, Kansas City, MO 64111 USA
Objective. To identify and characterize estrogen receptor (ER) transcripts expressed in immune cells of patients with systemic lupus erythematosus (SLE) and healthy donors. Methods, Peripheral blood monocytes and T cells were prepared from patients with SLE (n = 6) and healthy donors (n = 8). T cells were separated into CD4 and CD8. Some monocytes and T cells were stimulated with estradiol, PMA, and ionomycin. Epstein-Barr virus-transformed B cell lines (n = 7) and B cell hybridomas (n = 2) established from patients with SLE and a healthy individual were used as a B cell source. These cells were examined for ER mRNA by reverse transcription nested polymerase chain reaction. Amplified cDNA were sequenced by standard methods. Results. In all cells tested, ER mRNA was expressed without prior in vitro stimulation. Partial sequences from exons 1-8 were nearly identical to the published sequence of the human ER mRNA. There were no notable differences in the ER transcripts between patients and healthy controls, Variant receptor transcripts lacking exon 5 or exon 7, which encodes the hormone binding domain, were identified in the majority of the cells. Precise deletion of the exons suggests that they are alternatively spliced transcripts. Whether the detected transcripts are translated into functional receptor proteins remains to be determined. In vitro stimulation did not affect ER mRNA expression. The presence of variants did not correlate with disease activity or medication. Conclusion. Monocytes, T cells, and B cells in patients express transcripts of the normal wild type ER and the hormone binding domain variants in vivo.
机构:
Minist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, A Tsyb Med Radiol Res Ctr, Moscow, RussiaMinist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, A Tsyb Med Radiol Res Ctr, Moscow, Russia
Mushkarina, T.
Kuzmina, E.
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Minist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, A Tsyb Med Radiol Res Ctr, Moscow, RussiaMinist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, A Tsyb Med Radiol Res Ctr, Moscow, Russia
Kuzmina, E.
Konstantinova, T.
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Minist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, A Tsyb Med Radiol Res Ctr, Moscow, RussiaMinist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, A Tsyb Med Radiol Res Ctr, Moscow, Russia
Konstantinova, T.
Samborsky, S.
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Minist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, A Tsyb Med Radiol Res Ctr, Moscow, RussiaMinist Hlth Russian Federat, Branch Natl Med Res Radiol Ctr, A Tsyb Med Radiol Res Ctr, Moscow, Russia
机构:
Tokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Osaka Rheumatol Clin, Osaka, JapanTokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Ito, M. N.
Murakami, M.
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Tokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Osaka Rheumatol Clin, Osaka, JapanTokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Murakami, M.
Saito, M.
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Kyoto Univ, Ctr iPS Cells Res & Applicat, Kyoto, JapanTokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Saito, M.
Niwa, A.
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Kyoto Univ, Ctr iPS Cells Res & Applicat, Kyoto, JapanTokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Niwa, A.
Osawa, M.
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Kyoto Univ, Ctr iPS Cells Res & Applicat, Kyoto, JapanTokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Osawa, M.
Nakahata, T.
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Kyoto Univ, Ctr iPS Cells Res & Applicat, Kyoto, JapanTokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Nakahata, T.
Nishimoto, N.
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Tokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan
Osaka Rheumatol Clin, Osaka, JapanTokyo Med Univ, Inst Med Sci, Mol Regulat Intractable Dis, Tokyo, Japan