Absorption of intraarticularly injected horseradish peroxidase in synoviocytes of rat synovial membrane: An ultrastructural—cytochemical study

Pernille Møller Graab˦k
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引用次数: 14

Abstract

The ability of type A and type S synoviocytes to absorb horseradish peroxidase (HRP) and the intracellular fate of this tracer were studied by electron microscopic cytochemistry. Different concentrations of HRP (0.1–5 mg/ml) were injected into the left knee joint of rats and at intervals ranging from 1 min to 24 hr after injection the synovial membrane was fixed and incubated for HRP. Type A synoviocytes showed a striking ability to absorb HRP at low concentrations. At 1 and 5 min after injection reaction product was localized in coated pits and coated vesicles (110 nm) as well as in smooth-walled vesicles, vacuoles, and tubules. At 15 min to 4 hr postinjection the lysosomal system became increasingly loaded with reaction product. At 24 h after injection reaction product had disappeared. At higher concentrations of HRP similar observations were made in the A cells, but reaction product was still apparent in lysosomes at 24 hr postinjection. With respect to type S synoviocytes no reaction product was detected within these cells at any time interval after injection of low concentrations of HRP. However, at 5 min after injection of higher concentrations of HRP reaction product was localized in smooth vesicles and vacuoles mainly restricted to the large cytoplasmic processes facing the joint cavity. At 30 min to 4 hr postinjection the lysosomal system became progressively more loaded with HRP reaction product. At 24 hr after injection reaction product still remained in the lysosomal system.

The present findings that type A and type S synoviocytes showed major differences with respect to endocytic capacity and cellular structures involved in absorption of HRP support the interpretation that the A and S cells represent two distinct types of cells and further suggest that endocytosis in these two types of cells serve different functions.

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关节内注射辣根过氧化物酶在大鼠滑膜滑膜细胞中的吸收:超微结构-细胞化学研究
用电镜细胞化学方法研究了A型和S型滑膜细胞对辣根过氧化物酶(HRP)的吸收能力及其示踪剂在细胞内的作用。将不同浓度的HRP (0.1 ~ 5mg /ml)注射到大鼠左膝关节内,注射后1 min ~ 24 hr固定滑膜孵育HRP。A型滑膜细胞具有显著的低浓度HRP吸收能力。注射后1分钟和5分钟,反应产物定位于包被凹坑和包被囊泡(110 nm)以及光滑壁囊泡、液泡和小管。注射后15分钟至4小时,溶酶体系统的反应产物负荷逐渐增加。注射后24 h反应产物消失。在较高浓度的HRP下,在A细胞中也有类似的观察结果,但在注射后24小时溶酶体中仍有明显的反应产物。注射低浓度HRP后,S型滑膜细胞在任何时间间隔内均未检测到反应产物。然而,在注射高浓度HRP后5分钟,反应产物定位于光滑的囊泡和液泡中,主要局限于面向关节腔的大细胞质突。在注射后30分钟至4小时,溶酶体系统逐渐增加HRP反应产物的负荷。注射后24小时,反应产物仍留在溶酶体系统中。目前的研究结果显示,A型和S型滑膜细胞在参与HRP吸收的内吞能力和细胞结构方面存在重大差异,这支持了A和S细胞代表两种不同类型细胞的解释,并进一步表明这两种细胞的内吞作用具有不同的功能。
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