Characterization of the Immunoregulatory Action of Saikosaponin-d
The immunoregulatory action of saikosaponin-d (SSd), which was isolated from the root of Bupleurum falcatum L. and has a steroid-like structure, was examined on splenic T lymphocytes of C57BL/6 mice. SSd displayed a definite action in vitro to bidirectionally control the growth response of T lymphoc...
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Veröffentlicht in: | Cellular immunology 1994-11, Vol.159 (1), p.15-25 |
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creator | Kato, Masashi Pu, Mei-Yi Isobe, Ken-Ichi Iwamoto, Takashi Nagase, Fumihiko Lwin, Tint Zhang, Yue-Hua Hattori, Taku Yanagita, Noriyuki Nakashima, Izumi |
description | The immunoregulatory action of saikosaponin-d (SSd), which was isolated from the root of Bupleurum falcatum L. and has a steroid-like structure, was examined on splenic T lymphocytes of C57BL/6 mice. SSd displayed a definite action in vitro to bidirectionally control the growth response of T lymphocytes stimulated by concanavalin A, anti-CD3 monoclonal antibody, and calcium ionophore A23187 plus phorbol 12-myristate 13-acetate. Low concentrations (I-3 μg/ml) of SSd upregulated the responses to suboptimum stimuli of agonists, particularly during the relatively late stage of the responses, whereas it downregulated the responses to supraoptimal stimuli. Under appropriate experimental conditions, SSd promoted interleukin-2 (IL-2) production and IL-2 receptor expression. It also accelerated c-fos gene transcription, but it did not modulate the level of tyrosine phosphorylation of cellular proteins. We concluded from these results that SSd uniquely modulates T lymphocyte function and that at least one target of the action of SSd is located at or before the step of c-fos gene transcription and after T-cell receptor/CD3-mediated protein tyrosine kinase activation. |
doi_str_mv | 10.1006/cimm.1994.1291 |
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SSd displayed a definite action in vitro to bidirectionally control the growth response of T lymphocytes stimulated by concanavalin A, anti-CD3 monoclonal antibody, and calcium ionophore A23187 plus phorbol 12-myristate 13-acetate. Low concentrations (I-3 μg/ml) of SSd upregulated the responses to suboptimum stimuli of agonists, particularly during the relatively late stage of the responses, whereas it downregulated the responses to supraoptimal stimuli. Under appropriate experimental conditions, SSd promoted interleukin-2 (IL-2) production and IL-2 receptor expression. It also accelerated c-fos gene transcription, but it did not modulate the level of tyrosine phosphorylation of cellular proteins. We concluded from these results that SSd uniquely modulates T lymphocyte function and that at least one target of the action of SSd is located at or before the step of c-fos gene transcription and after T-cell receptor/CD3-mediated protein tyrosine kinase activation.</description><identifier>ISSN: 0008-8749</identifier><identifier>EISSN: 1090-2163</identifier><identifier>DOI: 10.1006/cimm.1994.1291</identifier><identifier>PMID: 7954839</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Adjuvants, Immunologic ; Animals ; Blotting, Northern ; Cell Division - drug effects ; Fluorescent Antibody Technique ; Genes, fos ; Glycyrrhetinic Acid - analogs & derivatives ; Glycyrrhetinic Acid - pharmacology ; Glycyrrhizic Acid ; Immunosuppressive Agents ; Interleukin-2 - biosynthesis ; Mice ; Mice, Inbred C57BL ; Oleanolic Acid - analogs & derivatives ; Phosphorylation ; Receptors, Interleukin-2 - biosynthesis ; Sapogenins - chemistry ; Sapogenins - pharmacology ; Saponins ; Signal Transduction ; Spleen - cytology ; Spleen - drug effects ; Spleen - immunology ; T-Lymphocytes - drug effects ; Tyrosine - metabolism ; Up-Regulation</subject><ispartof>Cellular immunology, 1994-11, Vol.159 (1), p.15-25</ispartof><rights>1994 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-1bd16e1dc2c2fdd8ead2bd8af623326e1e6832c7d485d34ec0c32339505d49563</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/cimm.1994.1291$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7954839$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kato, Masashi</creatorcontrib><creatorcontrib>Pu, Mei-Yi</creatorcontrib><creatorcontrib>Isobe, Ken-Ichi</creatorcontrib><creatorcontrib>Iwamoto, Takashi</creatorcontrib><creatorcontrib>Nagase, Fumihiko</creatorcontrib><creatorcontrib>Lwin, Tint</creatorcontrib><creatorcontrib>Zhang, Yue-Hua</creatorcontrib><creatorcontrib>Hattori, Taku</creatorcontrib><creatorcontrib>Yanagita, Noriyuki</creatorcontrib><creatorcontrib>Nakashima, Izumi</creatorcontrib><title>Characterization of the Immunoregulatory Action of Saikosaponin-d</title><title>Cellular immunology</title><addtitle>Cell Immunol</addtitle><description>The immunoregulatory action of saikosaponin-d (SSd), which was isolated from the root of Bupleurum falcatum L. and has a steroid-like structure, was examined on splenic T lymphocytes of C57BL/6 mice. SSd displayed a definite action in vitro to bidirectionally control the growth response of T lymphocytes stimulated by concanavalin A, anti-CD3 monoclonal antibody, and calcium ionophore A23187 plus phorbol 12-myristate 13-acetate. Low concentrations (I-3 μg/ml) of SSd upregulated the responses to suboptimum stimuli of agonists, particularly during the relatively late stage of the responses, whereas it downregulated the responses to supraoptimal stimuli. Under appropriate experimental conditions, SSd promoted interleukin-2 (IL-2) production and IL-2 receptor expression. It also accelerated c-fos gene transcription, but it did not modulate the level of tyrosine phosphorylation of cellular proteins. We concluded from these results that SSd uniquely modulates T lymphocyte function and that at least one target of the action of SSd is located at or before the step of c-fos gene transcription and after T-cell receptor/CD3-mediated protein tyrosine kinase activation.</description><subject>Adjuvants, Immunologic</subject><subject>Animals</subject><subject>Blotting, Northern</subject><subject>Cell Division - drug effects</subject><subject>Fluorescent Antibody Technique</subject><subject>Genes, fos</subject><subject>Glycyrrhetinic Acid - analogs & derivatives</subject><subject>Glycyrrhetinic Acid - pharmacology</subject><subject>Glycyrrhizic Acid</subject><subject>Immunosuppressive Agents</subject><subject>Interleukin-2 - biosynthesis</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Oleanolic Acid - analogs & derivatives</subject><subject>Phosphorylation</subject><subject>Receptors, Interleukin-2 - biosynthesis</subject><subject>Sapogenins - chemistry</subject><subject>Sapogenins - pharmacology</subject><subject>Saponins</subject><subject>Signal Transduction</subject><subject>Spleen - cytology</subject><subject>Spleen - drug effects</subject><subject>Spleen - immunology</subject><subject>T-Lymphocytes - drug effects</subject><subject>Tyrosine - metabolism</subject><subject>Up-Regulation</subject><issn>0008-8749</issn><issn>1090-2163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkDtPwzAURi0EKqWwsiFlYkvwI3Hssap4VKrEAMyWa99QQxIXO0Eqv55ELWyI6Q7n3G84CF0SnBGM-Y1xTZMRKfOMUEmO0JRgiVNKODtGU4yxSEWZy1N0FuMbxoTkEk_QpJRFLpicovlio4M2HQT3pTvn28RXSbeBZNk0fesDvPa17nzYJXPzg5-0e_dRb33r2tSeo5NK1xEuDneGXu5unxcP6erxfrmYr1KTM96lZG0JB2INNbSyVoC2dG2FrjhljA4EuGDUlDYXhWU5GGzYQGSBC5vLgrMZut7vboP_6CF2qnHRQF3rFnwfVckFLiX7XyS8EJiVo5jtRRN8jAEqtQ2u0WGnCFZjXDXGVWNcNcYdHq4Oy_26AfurH2oOXOw5DB0-HQQVjYPWgHUBTKesd39NfwNbloi1</recordid><startdate>19941101</startdate><enddate>19941101</enddate><creator>Kato, Masashi</creator><creator>Pu, Mei-Yi</creator><creator>Isobe, Ken-Ichi</creator><creator>Iwamoto, Takashi</creator><creator>Nagase, Fumihiko</creator><creator>Lwin, Tint</creator><creator>Zhang, Yue-Hua</creator><creator>Hattori, Taku</creator><creator>Yanagita, Noriyuki</creator><creator>Nakashima, Izumi</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19941101</creationdate><title>Characterization of the Immunoregulatory Action of Saikosaponin-d</title><author>Kato, Masashi ; Pu, Mei-Yi ; Isobe, Ken-Ichi ; Iwamoto, Takashi ; Nagase, Fumihiko ; Lwin, Tint ; Zhang, Yue-Hua ; Hattori, Taku ; Yanagita, Noriyuki ; Nakashima, Izumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-1bd16e1dc2c2fdd8ead2bd8af623326e1e6832c7d485d34ec0c32339505d49563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Adjuvants, Immunologic</topic><topic>Animals</topic><topic>Blotting, Northern</topic><topic>Cell Division - drug effects</topic><topic>Fluorescent Antibody Technique</topic><topic>Genes, fos</topic><topic>Glycyrrhetinic Acid - analogs & derivatives</topic><topic>Glycyrrhetinic Acid - pharmacology</topic><topic>Glycyrrhizic Acid</topic><topic>Immunosuppressive Agents</topic><topic>Interleukin-2 - biosynthesis</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Oleanolic Acid - analogs & derivatives</topic><topic>Phosphorylation</topic><topic>Receptors, Interleukin-2 - biosynthesis</topic><topic>Sapogenins - chemistry</topic><topic>Sapogenins - pharmacology</topic><topic>Saponins</topic><topic>Signal Transduction</topic><topic>Spleen - cytology</topic><topic>Spleen - drug effects</topic><topic>Spleen - immunology</topic><topic>T-Lymphocytes - drug effects</topic><topic>Tyrosine - metabolism</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kato, Masashi</creatorcontrib><creatorcontrib>Pu, Mei-Yi</creatorcontrib><creatorcontrib>Isobe, Ken-Ichi</creatorcontrib><creatorcontrib>Iwamoto, Takashi</creatorcontrib><creatorcontrib>Nagase, Fumihiko</creatorcontrib><creatorcontrib>Lwin, Tint</creatorcontrib><creatorcontrib>Zhang, Yue-Hua</creatorcontrib><creatorcontrib>Hattori, Taku</creatorcontrib><creatorcontrib>Yanagita, Noriyuki</creatorcontrib><creatorcontrib>Nakashima, Izumi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kato, Masashi</au><au>Pu, Mei-Yi</au><au>Isobe, Ken-Ichi</au><au>Iwamoto, Takashi</au><au>Nagase, Fumihiko</au><au>Lwin, Tint</au><au>Zhang, Yue-Hua</au><au>Hattori, Taku</au><au>Yanagita, Noriyuki</au><au>Nakashima, Izumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of the Immunoregulatory Action of Saikosaponin-d</atitle><jtitle>Cellular immunology</jtitle><addtitle>Cell Immunol</addtitle><date>1994-11-01</date><risdate>1994</risdate><volume>159</volume><issue>1</issue><spage>15</spage><epage>25</epage><pages>15-25</pages><issn>0008-8749</issn><eissn>1090-2163</eissn><abstract>The immunoregulatory action of saikosaponin-d (SSd), which was isolated from the root of Bupleurum falcatum L. and has a steroid-like structure, was examined on splenic T lymphocytes of C57BL/6 mice. SSd displayed a definite action in vitro to bidirectionally control the growth response of T lymphocytes stimulated by concanavalin A, anti-CD3 monoclonal antibody, and calcium ionophore A23187 plus phorbol 12-myristate 13-acetate. Low concentrations (I-3 μg/ml) of SSd upregulated the responses to suboptimum stimuli of agonists, particularly during the relatively late stage of the responses, whereas it downregulated the responses to supraoptimal stimuli. Under appropriate experimental conditions, SSd promoted interleukin-2 (IL-2) production and IL-2 receptor expression. It also accelerated c-fos gene transcription, but it did not modulate the level of tyrosine phosphorylation of cellular proteins. We concluded from these results that SSd uniquely modulates T lymphocyte function and that at least one target of the action of SSd is located at or before the step of c-fos gene transcription and after T-cell receptor/CD3-mediated protein tyrosine kinase activation.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>7954839</pmid><doi>10.1006/cimm.1994.1291</doi><tpages>11</tpages></addata></record> |
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subjects | Adjuvants, Immunologic Animals Blotting, Northern Cell Division - drug effects Fluorescent Antibody Technique Genes, fos Glycyrrhetinic Acid - analogs & derivatives Glycyrrhetinic Acid - pharmacology Glycyrrhizic Acid Immunosuppressive Agents Interleukin-2 - biosynthesis Mice Mice, Inbred C57BL Oleanolic Acid - analogs & derivatives Phosphorylation Receptors, Interleukin-2 - biosynthesis Sapogenins - chemistry Sapogenins - pharmacology Saponins Signal Transduction Spleen - cytology Spleen - drug effects Spleen - immunology T-Lymphocytes - drug effects Tyrosine - metabolism Up-Regulation |
title | Characterization of the Immunoregulatory Action of Saikosaponin-d |
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