{"title":"无血清培养基培养大鼠胸腺巨噬细胞的表型和粘附特性。","authors":"M Colić, D Drabek","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Rat thymic macrophages (TMF) were cultivated in serum-free medium (Biorich 2) using an explant technique. This medium favored the growth of macrophages and inhibited the proliferation of other non-lymphoid cells. Macrophage characteristics of cultivated cells were confirmed by their morphology, NSE activity and positivity (approx. 95%) with ED1 and Mar 1 mAbs (pan-macrophage markers in the rat). The majority of non-adherent cells (NAC) released in culture medium during the proliferation of TMF also possessed macrophage characteristics. Both adherent TMF and NAC were heterogeneous cells expressing cortical/CMZ phenotype (ED2+, R-MC 41+, R-MC 42+) and CMZ/medullary phenotype (R-MC 43+, R-MC 44+). NAC population contained higher proportion of cells expressing class II MHC molecules, IL-2R and 1F119 antigen compared to adherent TMF. The TMF phenotype changed during cultivation and upon stimulation with inflammatory cytokines (IL-1, IFN-gamma, TNF-alpha). TMF formed rosettes with syngeneic or allogeneic thymocytes both at 37 and 4 degrees C. The percentages of rosettes was dependent on the incubation time and TMF/thymocyte ratio. A higher percentage of immature thymocytes (CD4-CD8- or CD4+CD8+) bound to TMF compared to mature, cortisone-resistant thymocytes. The involvement of TMF membrane molecules in TMF/thymocyte adhesion was tested by preincubation of TMF with specific mAbs. It was found that Mar 1 mAb was partially inhibitory, OX-42 (anti CD11b) was slightly stimulatory, whereas other mAbs had no significant effect.</p>","PeriodicalId":76738,"journal":{"name":"Thymus","volume":"21 1","pages":"43-60"},"PeriodicalIF":0.0000,"publicationDate":"1993-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phenotype and adhesion characteristics of rat thymic macrophages cultivated in serum-free medium.\",\"authors\":\"M Colić, D Drabek\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Rat thymic macrophages (TMF) were cultivated in serum-free medium (Biorich 2) using an explant technique. This medium favored the growth of macrophages and inhibited the proliferation of other non-lymphoid cells. Macrophage characteristics of cultivated cells were confirmed by their morphology, NSE activity and positivity (approx. 95%) with ED1 and Mar 1 mAbs (pan-macrophage markers in the rat). The majority of non-adherent cells (NAC) released in culture medium during the proliferation of TMF also possessed macrophage characteristics. Both adherent TMF and NAC were heterogeneous cells expressing cortical/CMZ phenotype (ED2+, R-MC 41+, R-MC 42+) and CMZ/medullary phenotype (R-MC 43+, R-MC 44+). NAC population contained higher proportion of cells expressing class II MHC molecules, IL-2R and 1F119 antigen compared to adherent TMF. The TMF phenotype changed during cultivation and upon stimulation with inflammatory cytokines (IL-1, IFN-gamma, TNF-alpha). TMF formed rosettes with syngeneic or allogeneic thymocytes both at 37 and 4 degrees C. The percentages of rosettes was dependent on the incubation time and TMF/thymocyte ratio. A higher percentage of immature thymocytes (CD4-CD8- or CD4+CD8+) bound to TMF compared to mature, cortisone-resistant thymocytes. The involvement of TMF membrane molecules in TMF/thymocyte adhesion was tested by preincubation of TMF with specific mAbs. It was found that Mar 1 mAb was partially inhibitory, OX-42 (anti CD11b) was slightly stimulatory, whereas other mAbs had no significant effect.</p>\",\"PeriodicalId\":76738,\"journal\":{\"name\":\"Thymus\",\"volume\":\"21 1\",\"pages\":\"43-60\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1993-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Thymus\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Thymus","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Phenotype and adhesion characteristics of rat thymic macrophages cultivated in serum-free medium.
Rat thymic macrophages (TMF) were cultivated in serum-free medium (Biorich 2) using an explant technique. This medium favored the growth of macrophages and inhibited the proliferation of other non-lymphoid cells. Macrophage characteristics of cultivated cells were confirmed by their morphology, NSE activity and positivity (approx. 95%) with ED1 and Mar 1 mAbs (pan-macrophage markers in the rat). The majority of non-adherent cells (NAC) released in culture medium during the proliferation of TMF also possessed macrophage characteristics. Both adherent TMF and NAC were heterogeneous cells expressing cortical/CMZ phenotype (ED2+, R-MC 41+, R-MC 42+) and CMZ/medullary phenotype (R-MC 43+, R-MC 44+). NAC population contained higher proportion of cells expressing class II MHC molecules, IL-2R and 1F119 antigen compared to adherent TMF. The TMF phenotype changed during cultivation and upon stimulation with inflammatory cytokines (IL-1, IFN-gamma, TNF-alpha). TMF formed rosettes with syngeneic or allogeneic thymocytes both at 37 and 4 degrees C. The percentages of rosettes was dependent on the incubation time and TMF/thymocyte ratio. A higher percentage of immature thymocytes (CD4-CD8- or CD4+CD8+) bound to TMF compared to mature, cortisone-resistant thymocytes. The involvement of TMF membrane molecules in TMF/thymocyte adhesion was tested by preincubation of TMF with specific mAbs. It was found that Mar 1 mAb was partially inhibitory, OX-42 (anti CD11b) was slightly stimulatory, whereas other mAbs had no significant effect.