Norrby K, Jakobsson A, Sörbo J
Virchows Arch B Cell Pathol Incl Mol Pathol. 1986;52(3):195-206. doi: 10.1007/BF02889963.
The angiogenic effect of autogenous secreting mast cells (MCs) was studied using a novel experimental approach. The virtually avascular membranous rat mesentery was used as test tissue. The activation of MCs was elicited by repeated intraperitoneal injections of the MC-secretagogue compound 48/80, which per se appears inert from the proliferogenic and angiogenic point of view. Angiogenesis was quantitated histologically and expressed the number of vessels/unit length of mesentery. The smallest vessels recognized had a luminal area of approximately 7-8 microns 2 (corresponding to a circular diameter of 3.0-3.2 microns). Seven to ten days after MC-activation ended, the number of blood vessels had increased 7- to 6-fold. A retrogressive reaction occurred between days 21 and 38 after treatment, when the number of vessels had essentially normalized, as compared to vehicle-treated controls. The present study, introducing the membranous mesentery as a model for quantitative angiogenetic studies, provides evidence that MCs can induce angiogenesis, which is new. The possible therapeutic implication of this finding is noteworthy.
采用一种新的实验方法研究了自体分泌肥大细胞(MCs)的血管生成作用。将几乎无血管的大鼠膜性肠系膜用作测试组织。通过反复腹腔注射MC分泌刺激物化合物48/80来引发MCs的激活,从增殖和血管生成的角度来看,该化合物本身似乎无活性。通过组织学方法对血管生成进行定量,并表示为肠系膜单位长度的血管数量。识别出的最小血管的管腔面积约为7-8平方微米(对应于3.0-3.2微米的圆形直径)。MC激活结束后7至10天,血管数量增加了7至6倍。在治疗后第21天至38天之间出现了退行性反应,此时与用赋形剂处理的对照组相比,血管数量已基本恢复正常。本研究引入膜性肠系膜作为定量血管生成研究的模型,提供了MCs可诱导血管生成的证据,这是新的发现。这一发现可能的治疗意义值得关注。