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  • Quantification  (2)
  • Alkylation, enantioselective  (1)
  • 1
    ISSN: 1432-0878
    Keywords: Key words: In vivo ; Lymphocytes ; Migration ; Lymph nodes ; Peyer’s patches ; Microenvironment ; Quantification ; Rat (Lewis)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. The migration routes of lymphocyte subsets through organ compartments are of importance when trying to understand the local events taking place during immune responses. We have therefore studied the traffic of B, T, CD4+, and CD8+ lymphocytes through lymph nodes and Peyer’s patches. At various time points after injection into the rat, labeled lymphocytes were localized, and their phenotype characterized in cryostat sections using immunohistochemistry. Morphometry was also performed, and the recovery of 51Cr-labeled lymphocytes in these organs was determined. B and T lymphocytes entered the lymph nodes via the high endothelial venules in similar numbers. Most B lymphocytes migrated via the paracortex (T cell area) into the cortex (B cell area), and then back in substantial numbers into the paracortex. In contrast, T lymphocytes predominantly migrated into the paracortex and were rarely seen in the cortex. No obvious differences were seen between various lymph nodes and Peyer’s patches and the routes of CD4+ and CD8+ lymphocytes. After injection of lymphocytes into animals with autotransplanted splenic tissue, the number of B lymphocytes that had migrated into the B cell area of lymph nodes and of Peyer’s patches was significantly decreased, whereas CD4+ lymphocytes migrated in larger numbers into the T cell area of both organs.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    ISSN: 1432-0878
    Keywords: In vivo ; Lymphocytes ; Migration ; Lymph nodes ; Peyer's patches ; Microenvironment ; Quantification ; Rat (Lewis)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The migration routes of lymphocyte subsets through organ compartments are of importance when trying to understand the local events taking place during immune responses. We have therefore studied the traffic of B, T, CD4+, and CD8+ lymphocytes through lymph nodes and Peyer's patches. At various time points after injection into the rat, labeled lymphocytes were localized, and their phenotype characterized in cryostat sections using immunohistochemistry. Morphometry was also performed, and the recovery of 51Cr-labeled lymphocytes in these organs was determined. B and T lymphocytes entered the lymph nodes via the high endothelial venules in similar numbers. Most B lymphocytes migrated via the paracortex (T cell area) into the cortex (B cell area), and then back in substantial numbers into the paracortex. In contrast, T lymphocytes predominantly migrated into the paracortex and were rarely seen in the cortex. No obvious differences were seen between various lymph nodes and Peyer's patches and the routes of CD4+ and CD8+ lymphocytes. After injection of lymphocytes into animals with autotransplanted splenic tissue, the number of B lymphocytes that had migrated into the B cell area of lymph nodes and of Peyer's patches was significantly decreased, whereas CD4+ lymphocytes migrated in larger numbers into the T cell area of both organs.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1989 (1989), S. 1081-1083 
    ISSN: 0170-2041
    Keywords: Alkylation, enantioselective ; β-Ketophosphonate, chiral ; Oxazolidinones ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Einfache Darstellung von Dimethyl-[(3S)-3-methyl-2-oxo-5-octinyl]phosphonatDie diastereoselektive Alkylierung des chiralen Evans-Intermediates 2 mit 1-Iod-2-pentin (3) gibt das Oxazolidinon 4. Titanalkoxid-katalysierte Spaltung des Produktes zum Ethylester 5 und Acylierung von Methanphosphonsäure-dimethylester ergibt das chirale Phosphonat 6. Die optische Reinheit des Phosphonates 6 wird durch Trennung der Enantiomeren an einer chiralen HPLC-Säule und durch Umsetzung zum Bromketon 8 - einem Zwischenprodukt für das Prostacylin-Analoge ZK 96480 - belegt.
    Notes: The diastereoselective alkylation of the chiral Evans intermediate 2 with 1-iodo-2-pentyne (3) gives the oxazolidinone 4. Titanium alkoxide-catalysed cleavage yields the ethyl ester 5, which is used to acylate dimethyl methanephosphonate to the chiral phosphonate 6. The optical purity of phosphonate 6 is checked by separation on a chiral HPLC column and by conversion into the bromo ketone 8, an intermediate for the prostacyclin analogue ZK 96480.
    Type of Medium: Electronic Resource
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