Phytohemagglutinin isolectin stimulation of human lympocytes cultured in serum free medium

The ability of the red kidney bean (Phaseolus vulgaris) Phytohemagglutinin (PHA) isolectins L4 and E4 to transform human lymphocytes cultured in serum free or serum supplemented medium was studied. Previous similar studies done in fetal bovine serum (FBS) supplemented medium have shown L4 to be 30–6...

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Veröffentlicht in:Life sciences (1973) 1978-07, Vol.23 (3), p.237-245
Hauptverfasser: Egorin, Merrill J., Litvin, Forrest, Felsted, Ronald L., Bachur, Nicholas R.
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container_title Life sciences (1973)
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creator Egorin, Merrill J.
Litvin, Forrest
Felsted, Ronald L.
Bachur, Nicholas R.
description The ability of the red kidney bean (Phaseolus vulgaris) Phytohemagglutinin (PHA) isolectins L4 and E4 to transform human lymphocytes cultured in serum free or serum supplemented medium was studied. Previous similar studies done in fetal bovine serum (FBS) supplemented medium have shown L4 to be 30–60 times more potent a mitogen than E4. In serum free conditions, this difference was much less, L4 being only 3–9 times more potent than E4. In serum free medium, optimal mitogenic concentrations of L4 and E4 were 1.1.–3.3 ug/culture and 3.3–10 ug/culture respectively as compared to 3.3–10 ug/culture and 90–270 ug/culture for L4 and E4, respectively, in FBS suplemented medium. L4 stimulated lymphocytes in serum containing medium transform more rapidly than do L4 treated cells cultured in serum free conditions. Fetuin added to serum free cultures of lymphocytes more effectively inhibited transformation induced by E4 than by L4. Although the binding of 1251 E4 and L4 to lymphocytes was greatly reduced by the addition of FBS to the medium, the reduction in E4 binding was much greater than that in L4 binding. Neither L4 or E4 caused the death of lymphocytes cultured in serum free or FBS supplemented medium. These results confirm the previously described difference in mitogenic potential between L4 and E4. However, the results of earlier studies done in FBS supplemented medium include several artifacts related to the differential interaction of PHA isolections with fetuin and other serum glycoproteins.
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Previous similar studies done in fetal bovine serum (FBS) supplemented medium have shown L4 to be 30–60 times more potent a mitogen than E4. In serum free conditions, this difference was much less, L4 being only 3–9 times more potent than E4. In serum free medium, optimal mitogenic concentrations of L4 and E4 were 1.1.–3.3 ug/culture and 3.3–10 ug/culture respectively as compared to 3.3–10 ug/culture and 90–270 ug/culture for L4 and E4, respectively, in FBS suplemented medium. L4 stimulated lymphocytes in serum containing medium transform more rapidly than do L4 treated cells cultured in serum free conditions. Fetuin added to serum free cultures of lymphocytes more effectively inhibited transformation induced by E4 than by L4. Although the binding of 1251 E4 and L4 to lymphocytes was greatly reduced by the addition of FBS to the medium, the reduction in E4 binding was much greater than that in L4 binding. Neither L4 or E4 caused the death of lymphocytes cultured in serum free or FBS supplemented medium. These results confirm the previously described difference in mitogenic potential between L4 and E4. 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Previous similar studies done in fetal bovine serum (FBS) supplemented medium have shown L4 to be 30–60 times more potent a mitogen than E4. In serum free conditions, this difference was much less, L4 being only 3–9 times more potent than E4. In serum free medium, optimal mitogenic concentrations of L4 and E4 were 1.1.–3.3 ug/culture and 3.3–10 ug/culture respectively as compared to 3.3–10 ug/culture and 90–270 ug/culture for L4 and E4, respectively, in FBS suplemented medium. L4 stimulated lymphocytes in serum containing medium transform more rapidly than do L4 treated cells cultured in serum free conditions. Fetuin added to serum free cultures of lymphocytes more effectively inhibited transformation induced by E4 than by L4. Although the binding of 1251 E4 and L4 to lymphocytes was greatly reduced by the addition of FBS to the medium, the reduction in E4 binding was much greater than that in L4 binding. Neither L4 or E4 caused the death of lymphocytes cultured in serum free or FBS supplemented medium. These results confirm the previously described difference in mitogenic potential between L4 and E4. However, the results of earlier studies done in FBS supplemented medium include several artifacts related to the differential interaction of PHA isolections with fetuin and other serum glycoproteins.</description><subject>alpha-Fetoproteins - pharmacology</subject><subject>Cell Aggregation - drug effects</subject><subject>Cells, Cultured</subject><subject>Chromium Radioisotopes</subject><subject>Culture Media</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Lymphocyte Activation - drug effects</subject><subject>Phytohemagglutinins - isolation &amp; purification</subject><subject>Phytohemagglutinins - pharmacology</subject><subject>Stimulation, Chemical</subject><subject>Thymidine - metabolism</subject><subject>Time Factors</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1978</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxDAUhoMoOl6eQBdZiS6qJ007aTaCDN5A0IVu3IRMcupEmmZMGmHe3o4jLl2dA_8F_o-QEwYXDNj0EqCsCl5CfSaacwmcsUJukQlrhCxgytk2mfxZ9sh-Sh8AUNeC75KdBgRnE_L2vFgNYYFev793eXC966lLoUMz_jQNzudODy70NLR0kb3uabfyy2BWAyZqcjfkiJauvRizp21EpB6ty_6Q7LS6S3j0ew_I6-3Ny-y-eHy6e5hdPxamFDAUFq1FJrg1rRUVSNmw1lgAhiiktvNq3ugStKy5rLFuAKvKgG051MJwMbX8gJxuepcxfGZMg_IuGew63WPISYmKVaIUYjRWG6OJIaWIrVpG53VcKQZqDVStaak1LSUa9QNUyTF2_Nuf5-Oyv9APwVG92qg4TvxyGFUyDnszIogjRGWD-7_-G_S5hsg</recordid><startdate>19780717</startdate><enddate>19780717</enddate><creator>Egorin, Merrill J.</creator><creator>Litvin, Forrest</creator><creator>Felsted, Ronald L.</creator><creator>Bachur, Nicholas R.</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>7X8</scope></search><sort><creationdate>19780717</creationdate><title>Phytohemagglutinin isolectin stimulation of human lympocytes cultured in serum free medium</title><author>Egorin, Merrill J. ; Litvin, Forrest ; Felsted, Ronald L. ; Bachur, Nicholas R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c270t-dedde173dcfd7409981fcd001ee79adb4b8a20a95395e580e44c0df3057c376d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1978</creationdate><topic>alpha-Fetoproteins - pharmacology</topic><topic>Cell Aggregation - drug effects</topic><topic>Cells, Cultured</topic><topic>Chromium Radioisotopes</topic><topic>Culture Media</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Lymphocyte Activation - drug effects</topic><topic>Phytohemagglutinins - isolation &amp; purification</topic><topic>Phytohemagglutinins - pharmacology</topic><topic>Stimulation, Chemical</topic><topic>Thymidine - metabolism</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Egorin, Merrill J.</creatorcontrib><creatorcontrib>Litvin, Forrest</creatorcontrib><creatorcontrib>Felsted, Ronald L.</creatorcontrib><creatorcontrib>Bachur, Nicholas R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Egorin, Merrill J.</au><au>Litvin, Forrest</au><au>Felsted, Ronald L.</au><au>Bachur, Nicholas R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phytohemagglutinin isolectin stimulation of human lympocytes cultured in serum free medium</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>1978-07-17</date><risdate>1978</risdate><volume>23</volume><issue>3</issue><spage>237</spage><epage>245</epage><pages>237-245</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>The ability of the red kidney bean (Phaseolus vulgaris) Phytohemagglutinin (PHA) isolectins L4 and E4 to transform human lymphocytes cultured in serum free or serum supplemented medium was studied. Previous similar studies done in fetal bovine serum (FBS) supplemented medium have shown L4 to be 30–60 times more potent a mitogen than E4. In serum free conditions, this difference was much less, L4 being only 3–9 times more potent than E4. In serum free medium, optimal mitogenic concentrations of L4 and E4 were 1.1.–3.3 ug/culture and 3.3–10 ug/culture respectively as compared to 3.3–10 ug/culture and 90–270 ug/culture for L4 and E4, respectively, in FBS suplemented medium. L4 stimulated lymphocytes in serum containing medium transform more rapidly than do L4 treated cells cultured in serum free conditions. Fetuin added to serum free cultures of lymphocytes more effectively inhibited transformation induced by E4 than by L4. Although the binding of 1251 E4 and L4 to lymphocytes was greatly reduced by the addition of FBS to the medium, the reduction in E4 binding was much greater than that in L4 binding. Neither L4 or E4 caused the death of lymphocytes cultured in serum free or FBS supplemented medium. These results confirm the previously described difference in mitogenic potential between L4 and E4. However, the results of earlier studies done in FBS supplemented medium include several artifacts related to the differential interaction of PHA isolections with fetuin and other serum glycoproteins.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>80731</pmid><doi>10.1016/0024-3205(78)90311-9</doi><tpages>9</tpages></addata></record>
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subjects alpha-Fetoproteins - pharmacology
Cell Aggregation - drug effects
Cells, Cultured
Chromium Radioisotopes
Culture Media
Humans
In Vitro Techniques
Lymphocyte Activation - drug effects
Phytohemagglutinins - isolation & purification
Phytohemagglutinins - pharmacology
Stimulation, Chemical
Thymidine - metabolism
Time Factors
title Phytohemagglutinin isolectin stimulation of human lympocytes cultured in serum free medium
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