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培养的淋巴结巨噬细胞的DNA合成及白细胞介素1的产生。

DNA synthesis and production of interleukin 1 by lymph node macrophages in culture.

作者信息

Mastro A M, Bortner D M, Pishak S A

出版信息

J Leukoc Biol. 1986 Jan;39(1):63-75. doi: 10.1002/jlb.39.1.63.

Abstract

When bovine lymph node cells are cultured for several days the adherent macrophage population increases by as much as tenfold. This increase in cell number is primarily due to cell division, which reaches a maximum on day 4 or 5 of culture. Although the presence of the nonadherent cells seems required for cell division, we have been unable to detect a macrophage growth factor in either the nonadherent cell populations. The adherent cells were identified as macrophages based on positive esterase staining, the presence of Fc receptors, beta-glucuronidase activity, and phagocytosis. Moreover, these adherent cells produced interleukin 1 (IL1) after exposure to lipopolysaccharide in serum-free medium. Approximately 10(7) macrophages were stimulated to produce about 900 units of IL1 in a 24-hr period. Thus, the bovine lymph node preparation is a potential source of a large number of macrophages capable of dividing in culture and of producing IL1.

摘要

当牛淋巴结细胞培养数天时,贴壁巨噬细胞群体可增加多达10倍。细胞数量的这种增加主要是由于细胞分裂,在培养的第4天或第5天达到最大值。尽管非贴壁细胞的存在似乎是细胞分裂所必需的,但我们在任何一个非贴壁细胞群体中都未能检测到巨噬细胞生长因子。根据阳性酯酶染色、Fc受体的存在、β-葡萄糖醛酸酶活性和吞噬作用,将贴壁细胞鉴定为巨噬细胞。此外,这些贴壁细胞在无血清培养基中暴露于脂多糖后产生白细胞介素1(IL1)。在24小时内,大约10^7个巨噬细胞被刺激产生约900个IL1单位。因此,牛淋巴结制剂是大量巨噬细胞的潜在来源,这些巨噬细胞能够在培养中分裂并产生IL1。

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