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血管内皮作为粒细胞生成的调节因子:培养的人内皮细胞产生集落刺激活性。

Vascular endothelium as a regulator of granulopoiesis: production of colony-stimulating activity by cultured human endothelial cells.

作者信息

Quesenberry P J, Gimbrone M A

出版信息

Blood. 1980 Dec;56(6):1060-7.

PMID:6969095
Abstract

Colony-stimulating activity is a regulatory factor(s) that promotes differentiation of hemopoietic stem cells to mature granulocytes and macrophages; in man it has been found that blood monocytes, lymphocytes, and tissue macrophages produce it. In an effort to identify other potenitally physiologic tissue sources of colony-stimulating activity, we have studied the capacity of primary cultures of human vascular endothelial cells to produce colony-stimulating activity. Medium conditioned by incubation with endothelial cultures contained activity that promoted granulocyte-macrophage colony formation of nonadherent human and murine marrow cells. Exposure of endothelial cultures to 0.1-5.0 microgram/ml S. typhosa endotoxin for 6-72 hr enhanced colony-stimulating activity production. Similarly, incubation of endothelial cells with lysates of human blood granulocytes, or cocultivation with intact granulocytes, resulted in increased colony-stimulating activity levels. In 7-14 day cultures, freshly isolated endothelial cells, incorporated into agar underlayers, consistently stimulated more colony formation by nonadherent human marrow cells than comparable numbers of blood monocytes. These data indicate that: (1) cultured human endothelial cells are a potent source of colony-stimulating activity; (2) they respond to endotoxin and granulocytes and their contents by producing increased amounts of CSA; and (3) they produce morea colony-stimulating activity, than human blood monocytes under standardized conditions in vitro. These observations suggest that the vascular endothelium may play a role in the physiologic regulation of granulopoiesis.

摘要

集落刺激活性是一种调节因子,可促进造血干细胞分化为成熟的粒细胞和巨噬细胞;在人类中,已发现血液单核细胞、淋巴细胞和组织巨噬细胞可产生这种因子。为了确定集落刺激活性的其他潜在生理组织来源,我们研究了人血管内皮细胞原代培养物产生集落刺激活性的能力。与内皮细胞培养物一起孵育的条件培养基含有促进非贴壁人类和小鼠骨髓细胞的粒细胞 - 巨噬细胞集落形成的活性物质。将内皮细胞培养物暴露于0.1 - 5.0微克/毫升伤寒沙门氏菌内毒素6 - 72小时可增强集落刺激活性的产生。同样,将内皮细胞与人血粒细胞裂解物一起孵育,或与完整的粒细胞共培养,会导致集落刺激活性水平升高。在7 - 14天的培养物中,新鲜分离的内皮细胞掺入琼脂底层,与相当数量的血液单核细胞相比,始终能刺激更多非贴壁人类骨髓细胞形成集落。这些数据表明:(1)培养的人内皮细胞是集落刺激活性的强大来源;(2)它们通过产生更多的集落刺激活性来对内毒素、粒细胞及其成分作出反应;(3)在体外标准化条件下,它们比人类血液单核细胞产生更多的集落刺激活性。这些观察结果表明血管内皮可能在粒细胞生成的生理调节中发挥作用。

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