期刊文献+

多核巨细胞在人发生物材料降解中的超微观察 被引量:1

Ultrastructural observation of multinuclear giant cell during the process of degeneration and clearing of human hair
下载PDF
导出
摘要 目的:在超微结构水平观察人发生物材料修复周围神经缺损过程中自身的降解与多核巨细胞的关系。方法:制备SD大鼠坐骨神经缺损模型,用人发生物材料来桥接缺损的坐骨神经,电镜观察巨噬细胞与多核巨细胞对降解的人发生物材料吞噬消化过程。结果:术后3周,巨噬细胞聚集在人发周围,毛小皮已经开始剥脱断裂;6周时,人发周围出现由多个巨噬细胞融合形成的多核巨细胞,均质状的崩解颗粒及部分毛小皮碎片被巨噬细胞吞噬;12周时,有些皮质颗粒已降解为角蛋白细丝,巨噬细胞内含有大量颗粒。结论:在人发生物材料的降解过程中,多核巨细胞作为屏障隔离了材料和宿主组织细胞,毛小皮断裂的碎片和疏松的皮质颗粒,被巨噬细胞所吞噬,然后在大量溶酶体酶的水解下,完成对人发生物材料的清除。 Objective: To observe the changes ofmultinuclear giant cell during the process of degeneration and elimination of human hair in repairing injured peripheral nerve. Methods: To prepare the SD rat model of sciatic nerve damage, and implant the human hair. Electronic microscopy was performed to explore the ultrastructural changes ofmultinuclear giant cell during the process of degeneration and clearing of human hair. Results: The hair cuticle was denudated and degraded at the 3rd week. The human hair was surrounded by many macrophages. At the 6th week after the human hair implantation, the human hair biomaterial was surrounded by multinuclear giant cells fused by many macrophages. Human hair cortex was homogenous and began to collapse. The fragments of human hair were surrounded and wrapped by macrophages. At the 12th week, some human hair was degenerated into filament and granules which were wrapped and degenerated by macrophages. Conclusions: During the process of degeneration of human hair, multinuclear giant cells isolate the biomaterial and the host organization cell as the barrier. The deciduous fragments of human hair are wrapped, digested and eliminated by lysosomal enzyme in macrophages.
出处 《中国临床解剖学杂志》 CSCD 北大核心 2008年第3期315-317,共3页 Chinese Journal of Clinical Anatomy
基金 国家自然科学基金资助项目(30070368)
关键词 人发 生物材料 巨噬细胞 多核巨细胞 human hair biomaterial macrophage multinuclear giant cell
  • 相关文献

参考文献8

二级参考文献33

  • 1朴英杰.去分化与细胞组织损伤再生[J].第一军医大学学报,2004,24(7):736-737. 被引量:6
  • 2刘连璞,曹启迪,肖焕才,安连兵,黄辉,朴英杰.109HH人工腱在兔体内腱化过程的电镜观察[J].中华外科杂志,1995,33(9):523-525. 被引量:26
  • 3[1]Fernandez VC, Bunge RP, Bunge MB. Schwann cells degrade myelin and proliferate in the absence of macrophages: evidence from in vitro studies of Wallerian degeneration [ J ]. J Neurocytol, 1995, 24(9): 667-79.
  • 4[2]Holtzman E, NovikoffAB. Lysosomes in the rat sciatic nerve following crush[J]. J Cell Biol, 1965, 27: 651-69.
  • 5[3]Beuche W, Friede RL. The role of non-resident cells in Wallerian degeneration[J]. J Neurocytol, 1984, 13(5): 767-96.
  • 6[4]Crang AJ, Blakemore WF. Observations on Wallerian degeneration in explant cultures of cat sciatic nerve[J]. J Neurocytol, 1986, 15(4): 471-82.
  • 7[5]Shen 7L, Lassner F, Bader A, et al. Cellular activity of resident macrophages during Wallerian degeneration [J]. Microsurgery,2000, 20(5): 255-61.
  • 8[6]Jander S, Lausberg F, Stoll G. Differential recruitment ofCDS+ macrophages during Wallerian degeneration in the peripheral end central nervous system[J]. Brain Pathol, 2001, 11(1): 27-38.
  • 9[7]Hirata K, Kawabuchi M. Myelin phagocytosis by macrophages and nonmacrophages during Wallerian degeneration [J]. Microsc Res Tech, 2002, 57(6): 541-7.
  • 10[8]Hah MH, Piao YJ, Guo DW, et al. The role of Schwann cells and macrophages in the removal of myelin during wallerian degeneration [J]. Acta Histochem Cytochem, 1989, 22(2): 161-72.

共引文献27

同被引文献1

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部