Dow P R, Shinn S L, Ovale W K
Am J Anat. 1980 Apr;157(4):375-88. doi: 10.1002/aja.1001570406.
The permeability of the normal muscle spindle capsule to the entrance of an exogenous protein tracer was assessed by the use of horseradish peroxidase (HRP). Adult mice were injected intravenously with a solution of HRP (MW 40,000). After varying intervals, ranging from two to 240 minutes, animals were perfused aortically with fixative, and anterior tibialis muscles were removed, processed, and examined. The results were evaluated by electron microscopic cytochemical techniques, and attention was directed to the movement of tracer and its relationship to the outer and inner capsule of the muscle spindle. HRP was first demonstrated in cytoplasmic vesicles crossing the continuous capillary endothelium supplying the muscle spindle, and was then detected in the interstitial space surrounding the outer capsule. In polar regions, HRP had entered the periaxial space by two minutes, and it was seen in cytoplasmic vesicles of the attenuated outer capsule. Later, HRP abutted the sarcolemma of intrafusal fibers, and by 12.5 minutes there was evidence of tracer in T-tubules of these muscle cells. Whereas at no time was tracer observed traversing any of the numerous intracellular junctions of the capsule, it appeared that polar regions were leaky and open-ended at their distal portions. The sensory equatorial zone was considerably less permeable to the entrance of tracer. Whereas HRP was visible intially in cytoplasmic vesicles of the subjacent capillary endothelium, it was not until 12.5 minutes that racer could be demonstrated within some vesicles of equatorial outer capsule cells. At later times, a small amount of HRP was observed in the equatorial periaxial space, where it was phagocytosed and finally sequestered by cells of the inner capsule as membrane-bound lysosomal deposits. Consequently, at no time was tracer incorported into either intrafusal fibers or their sensory nerve terminals. Thus, in contract to polar regions, the muscle spindle capsule in the equatorial zone appears to be effective in preventing the indiscriminate penetration of HRP from the bloodstream. This suggests dissimilar paths of tracer movement from the microvasculature into sensory and non-sensory regions of the muscle spindle.
利用辣根过氧化物酶(HRP)评估正常肌梭囊对外源性蛋白质示踪剂进入的通透性。给成年小鼠静脉注射HRP(分子量40,000)溶液。在2至240分钟的不同间隔后,通过主动脉灌注固定剂处死动物,取出胫前肌,进行处理并检查。通过电子显微镜细胞化学技术评估结果,并关注示踪剂的移动及其与肌梭外囊和内囊的关系。HRP首先在穿过供应肌梭的连续毛细血管内皮的细胞质小泡中被发现,然后在围绕外囊的间质空间中被检测到。在两极区域,HRP在两分钟时已进入轴周间隙,并在变薄的外囊的细胞质小泡中可见。后来,HRP邻近视神经纤维的肌膜,到12.5分钟时,在这些肌细胞的T小管中有示踪剂存在的证据。尽管在任何时候都未观察到示踪剂穿过囊的众多细胞间连接,但似乎两极区域在其远端部分是渗漏的且开口的。感觉赤道区对示踪剂进入的通透性要低得多。虽然HRP最初在相邻毛细血管内皮的细胞质小泡中可见,但直到12.5分钟时,示踪剂才在赤道外囊细胞的一些小泡中被证实存在。在更晚的时候,在赤道轴周间隙中观察到少量HRP,它被内囊细胞吞噬,最终作为膜结合溶酶体沉积物被内囊细胞隔离。因此,示踪剂在任何时候都未被纳入神经纤维或其感觉神经末梢。因此,与两极区域不同,赤道区的肌梭囊似乎能有效防止HRP从血流中无差别地渗透。这表明示踪剂从微脉管系统进入肌梭感觉和非感觉区域的路径不同。