首页> 美国卫生研究院文献>British Journal of Experimental Pathology >Penetration of colloidal carbon through post-capillary venules in lymph nodes and peyers patches of the guinea-pig: a potential immunogeneic route.
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Penetration of colloidal carbon through post-capillary venules in lymph nodes and peyers patches of the guinea-pig: a potential immunogeneic route.

机译:胶体碳通过豚鼠的淋巴结和淋巴结中的毛细血管后小静脉渗透:一种潜在的免疫原性途径。

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摘要

Colloidal carbon injected intravascularly provided a selective marker for post-capillary venules in lymph nodes and Peyer's patches. In the first few minutes a denticulate outline to the lumen was formed by carbon capping the high columnar epithelium and carbon particles were deeply embedded between endothelial cells. Ten minutes after injection carbon had reached the basement membrane and was lying outside this membrane 30 min later, at first free but later engulfed inside macrophages. Carbon was retained in post-capillary venules for the duration of the experiment (8 h). Discontinuities were present in the basement membane in about one-fifth of venules, and lymphocyte and macrophage penetrating the basement membrane are demonstrated. It is postulated that carbon penetrates the post-capillary venular wall by increased intraluminal hydrostatic pressure arising from contraction of muscles that surrounded the lymphoid tissue in the case of the gut, or skeletal muscle compressing lymph nodes against a bony surface in the axilla, groin or neck. Secondly, if carbon is a model for particulate antigens, then post-capillary venules provide a potential immunogenic route whereby antigens can reach lymphoid tissues from the circulation, as proposed by Burwell (1962) for transplantation antigens.
机译:血管内注射的胶体碳为淋巴结和Peyer斑中的毛细血管后小静脉提供了选择性标记。在最初的几分钟内,通过碳覆盖高柱状上皮形成管腔的细小轮廓,并且碳颗粒深深地嵌入内皮细胞之间。注入十分钟后,碳已经到达基底膜,并在30分钟后躺在膜的外面,最初游离但后来被巨噬细胞吞噬。在实验期间(8小时),碳保留在毛细管后的小静脉中。在约五分之一的小静脉中,基底膜存在不连续性,并证明了穿透基底膜的淋巴细胞和巨噬细胞。据推测,在肠道的情况下,由于包围淋巴组织的肌肉收缩引起的管腔内静水压升高,或者骨骼肌将淋巴结压向腋窝,腹股沟或腹股沟的骨表面,从而使碳渗透通过毛细血管后小静脉壁。颈部。其次,如果碳是微粒抗原的模型,那么毛细血管后小静脉提供了一种潜在的免疫原性途径,使抗原可以从循环中到达淋巴组织,如Burwell(1962)提出的移植抗原。

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