Georgescu H I, Mendelow D, Evans C H
Ferguson Laboratory for Orthopaedic Research, University of Pittsburgh, School of Medicine, Pennsylvania 15261.
In Vitro Cell Dev Biol. 1988 Oct;24(10):1015-22. doi: 10.1007/BF02620875.
We have isolated a continuous cell line from soft tissue lining the knee joints of rabbits. Designated HIG-82, this line was produced by spontaneous establishment of an aging, late-passage culture of primary cells. Like unpassaged, primary cells, HIG-82 cells can be activated by a number of stimuli, including phorbol myristate acetate (PMA), interleukin-1 (IL-1), and the endocytosis of latex beads. Activated cells secrete collagenase, gelatinase, caseinase (stromelysin), and prostaglandin E2 (PGE2) into their culture medium. Pseudodiploid, HIG-82 cells combine a high plating efficiency with a doubling time of approximately 24 h. As primary tissue of this origin is difficult to obtain in large quantities and shows cellular heterogeneity, the HIG-82 cell line should facilitate research into the biology and biochemistry of the fibroblastic cells that line the diarthrodial joints of mammals. Such cells are likely to be important in the pathophysiology of various arthritides.
我们从兔膝关节的软组织中分离出了一个连续细胞系。该细胞系命名为HIG-82,是通过原代细胞老化、传代后期的自发建立而产生的。与未传代的原代细胞一样,HIG-82细胞可被多种刺激激活,包括佛波酯(PMA)、白细胞介素-1(IL-1)以及乳胶珠的内吞作用。激活的细胞会向其培养基中分泌胶原酶、明胶酶、酪蛋白酶(基质溶解素)和前列腺素E2(PGE2)。HIG-82细胞为假二倍体,具有较高的接种效率,倍增时间约为24小时。由于这种来源的原代组织难以大量获取且表现出细胞异质性,HIG-82细胞系应有助于对哺乳动物滑膜关节内衬的成纤维细胞的生物学和生物化学进行研究。这类细胞可能在各种关节炎的病理生理学中具有重要意义。