Norrby K, Jakobsson A, Sörbo J
Department of Pathology, University of Gothenburg, Sahlgren's Hospital, Sweden.
Virchows Arch B Cell Pathol Incl Mol Pathol. 1989;57(4):251-6. doi: 10.1007/BF02899089.
The activation of the autogenous mast cells (MCs) in situ in intact mesenterial windows was elicited by the intraperitoneal injection of the MC secretagogue Compound 48/80 over a period of 1, 3 and 5 days in Sprague-Dawley rats and in C57 BL/6 and CBA/Ca mice. As a probe of MC secretion, the release of histamine was quantified fluorometrically at predetermined intervals during the treatment. Fourteen days after the start of the treatment, the angiogenic response was quantified histologically as the number of vessel profiles per unit length of mesenteric window. Both the MC-activating and the angiogenic effect of the 48/80-treatment was greater in the rats than in the mice. The occurrence of MC-mediated angiogenesis in the mouse is demonstrated here for the first time. In the rat, 48/80-induced MC mediated angiogenesis increased in a distinctly dose-dependent manner. Two daily doses of 48/80 was the most efficient angiogenic protocol tested; a single day's treatment increased the number of vessels almost fivefold. The remarkable potency of the angiogenic reaction following MC secretion supports our previous notion that MC-mediated angiogenesis may have therapeutic implications in poorly vascularized tissues.
在完整的肠系膜窗原位激活自身肥大细胞(MCs),方法是在1天、3天和5天的时间内,给Sprague-Dawley大鼠以及C57 BL/6和CBA/Ca小鼠腹腔注射MC促分泌剂化合物48/80。作为MC分泌的指标,在治疗期间的预定时间间隔,通过荧光法对组胺的释放进行定量。治疗开始14天后,通过组织学方法对血管生成反应进行定量,以肠系膜窗单位长度内的血管轮廓数量表示。48/80治疗的MC激活和血管生成作用在大鼠中比在小鼠中更强。本文首次证明了小鼠中存在MC介导的血管生成。在大鼠中,48/80诱导的MC介导的血管生成以明显的剂量依赖性方式增加。每天两次注射48/80是测试的最有效的血管生成方案;单次治疗使血管数量增加了近五倍。MC分泌后血管生成反应的显著效力支持了我们之前的观点,即MC介导的血管生成可能对血管化不良的组织具有治疗意义。