£64.33

Springer Histamin und Histamin-Rezeptor-Antagonisten (Monographien aus dem Gesamtgebiet der Physiologie der Pflanzen und der Tiere)

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Last 56 days • 56 data points (No recent data available)

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£64.98 £64.27 £64.42 £64.58 £64.73 £64.89 £65.05 14 March 2026 27 March 2026 10 April 2026 24 April 2026 08 May 2026

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15 days · current 41 days 0 10 21 31 41 £64 £65 Days at Price

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Description

Die Mastze11e mit ihren 500-1000 metachromatischen Granula im Zytoplasma kommt praktisch in allen Bindegewebsstrukturen des Korpers vor [72]. Sie ist bevorzugt entlang der Blut- und Lymphgefaaverlaufe vor a11em im Be reich der terminalen Strombahn im lockeren Stromagewebe lokalisiert. In den parenchymatosen Organen, die nur wenig Bindegewebe enthalten, wie z.B. der Leber, Niere und im Herzmuskel finden sich die Mastzellen im Bereich der Adventitia der Gefaaverlaufe und im regionaren Bindegewebe. Die Anzahl in diesen parenchymatosen Organen ist damit relativ gering. Die groate Anzahl der Mastzellen wird in den serosen Hauten,wie Pleura, Pericard, Peritoneum sowie in den Meningen gefunden, ferner im Corium der Haut und hier besonders an den Akren. Nahezu 100% des hohen Gewebshist aminspiegels sind in diesen Zellen deponiert [1,39,46,67,75,78]. Die Gewebsmastze11en zeigen gegenuber den Blutbasophilen wesentliche Unterschiede: Letztere enthalten wesentl ich weniger Granula und zeiger:! keine positive Naphthol-ASD-Chloracetat-Esterase-Reaktion [49].Die Granula der Gewebsmastzellen beinhalten das Proteoglycan Heparin, die Blutbasophi len Chondoitin-Sulfat [3]. Die ze11uliire Ausstattung mit Inhaltsstoffen und die Funktion der Mastzellen in den verschiedenen Organen ist ebenfalls unterschiedlich. HERKUNFT, ENTWICKLUNG UND STRUKTUR DER HASTZELLEN Lennert und Parwaresch [49] konnten immunhistochemische Hinweise dafur finden, daa die Mastze11en sich aus der myelomonozytaren Reihe ableiten. Als wichtigste Hinweise fuhren die Autoren folgende Punkte auf: 1. Nachwe i s von Obergangs formen zwi schen Monozyten und Mastze 11 en nach massiver Mastzelldestruktion. 2. Zytolytische Effekte an Mastzellen durch hochspezifische autologe Makrophagenseren. 3. Vorkommen einer KCN-sensitiven Myeloperoxydase in unreifen Rattenmast zellen.

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