Yen S E, Stewart C C
In Vitro. 1981 Oct;17(10):871-76. doi: 10.1007/BF02618282.
The murine peritoneal cavity contains factors that inhibit the in vitro growth and colony formation of macrophages. The inhibition of macrophage growth is not due to cell death. In the presence of inhibitors, the growth of colony-forming macrophages is suppressed, and small clusters are formed as a result of limited proliferation. The more mature mononuclear phagocytes (blood monocytes and peritoneal exudate macrophages) are more sensitive to the overall inhibitory effect of the peritoneal inhibitors than the less mature bone marrow mononuclear phagocytes. Furthermore, using dialysis and Amicon ultrafiltration, at least two inhibitors with differential inhibitory effects can be demonstrated. The colony formation of bone marrow mononuclear phagocytes is suppressed mainly by a protease-resistant, small molecular weight (less than 1,000) dialyzable inhibitor. In contrast, peritoneal exudate macrophages are sensitive to both the small molecular weight inhibitor and a protease-sensitive, large molecular weight (greater than 12,000), nondialyzable inhibitor. The data suggest a possible existence of a dual inhibitor control on the proliferation of mononuclear phagocytes in vivo. In addition, the in vitro cultured peritoneal exudate cells are capable of producing inhibitors that mimic the activity of the in vivo inhibitors.
小鼠腹腔内含有抑制巨噬细胞体外生长和集落形成的因子。巨噬细胞生长的抑制并非由于细胞死亡。在存在抑制剂的情况下,集落形成巨噬细胞的生长受到抑制,由于增殖受限而形成小细胞簇。与不太成熟的骨髓单核吞噬细胞相比,更成熟的单核吞噬细胞(血液单核细胞和腹腔渗出巨噬细胞)对腹腔抑制剂的总体抑制作用更敏感。此外,通过透析和密理博超滤,可以证明至少有两种具有不同抑制作用的抑制剂。骨髓单核吞噬细胞的集落形成主要受到一种耐蛋白酶、小分子质量(小于1000)的可透析抑制剂的抑制。相比之下,腹腔渗出巨噬细胞对小分子质量抑制剂和一种蛋白酶敏感、大分子质量(大于12000)的不可透析抑制剂均敏感。数据表明体内单核吞噬细胞增殖可能存在双重抑制剂控制。此外,体外培养的腹腔渗出细胞能够产生模拟体内抑制剂活性的抑制剂。