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金鱼视网膜顶盖投射的活动驱动锐化:频闪照明下的发育会阻止锐化。

Activity-driven sharpening of the retinotectal projection in goldfish: development under stroboscopic illumination prevents sharpening.

作者信息

Schmidt J T, Buzzard M

机构信息

Department of Biological Sciences, State University of New York, Albany 12222.

出版信息

J Neurobiol. 1993 Mar;24(3):384-99. doi: 10.1002/neu.480240310.

Abstract

Blocking or synchronizing activity during regeneration of the retinotectal projection prevents both the sharpening of the retinotopic map recorded on tectum and the refinement of the structure of individual arbors within the plane of the map, and this refinement is triggered by N-methyl-D-aspartate (NMDA) receptors. We tested whether activity-driven refinement also occurs during development of the projection in larval and young adult goldfish. Shortly after hatching, larval goldfish were placed into tanks within light-tight chambers illuminated by a xenon strobe at 1 Hz for 14 h of each daily cycle. Fish were reared for 1.5-2 years, until large enough to record in our retinotectal mapping apparatus (6 cm length). Age- and size-matched controls had normal maps with multiunit receptive fields (MURFs) recorded at each tectal point of 10.8 degrees (0.16 S.E.M., n = 5), whereas the strobe-reared fish had only roughly retinotopic maps with much enlarged MURFs averaging 26.7 degrees (1.41 S.E.M., n = 5). This enlargement represents an abnormal convergence onto each tectal point, as the maps failed to sharpen during development. The arbors of individual retinal axons were stained with horseradish peroxidase (HRP) in larval fish and in adult strobe-reared and control fish. They were drawn with camera lucida from tectal whole mounts, and analyzed for spatial extent in the plane of the retinotopic map, order of branching, number of branch endings, depth of termination, and caliber of the parent axon. Arbors from larval fish (1-2 weeks) were small (approximately 50 x 40 microns) with less than 10 branches, occupied a single strata, and could not be separated into different classes by caliber of axon. The 87 arbors stained in control adult fish (6 cm long) were much like previously examined adult arbors, with those from fine, medium, and coarse axons averaging 115, 166, and 194 microns in extent, respectively, and having 17-24 branch endings. The 110 arbors from 12 strobe-reared fish were often abnormal. Although the fasciculation was normal, the extrafascicular routes were abnormal with reversing turns. The axons often had branches along their course, and these branches were scattered across a wider extent, rather than forming a distinct cluster. In contrast, neither the number of branches nor the depths of termination was significantly changed in any group. The coarse caliber arbors were most abnormal, being 64% longer and 30% wider than controls. The fine caliber arbors were also significantly larger by about 20%, but the medium caliber arbors were not enlarged.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在视网膜顶盖投射再生过程中阻断或同步活动,会阻止记录在顶盖上的视网膜拓扑图的锐化以及该图平面内单个树突结构的细化,而这种细化是由N-甲基-D-天冬氨酸(NMDA)受体触发的。我们测试了活动驱动的细化在幼体和年轻成年金鱼投射发育过程中是否也会发生。孵化后不久,将幼体金鱼放入不透光的暗箱中的水箱中,每个日周期用氙频闪灯以1赫兹的频率照射14小时。将鱼饲养1.5至2年,直到长得足够大可以在我们的视网膜顶盖映射装置中进行记录(体长6厘米)。年龄和大小匹配的对照组具有正常的图谱,在每个顶盖点记录的多单位感受野(MURF)为10.8度(0.16标准误,n = 5),而频闪灯饲养的鱼只有大致的视网膜拓扑图,MURF大大扩大,平均为26.7度(1.41标准误,n = 5)。这种扩大代表了在发育过程中每个顶盖点上异常的汇聚,因为图谱未能锐化。在幼体鱼以及成年频闪灯饲养和对照鱼中,用辣根过氧化物酶(HRP)对单个视网膜轴突的树突进行染色。从顶盖整装标本用明箱绘图仪绘制它们,并分析其在视网膜拓扑图平面内的空间范围、分支顺序、分支末端数量、终止深度以及母轴突的直径。幼体鱼(1至2周)的树突较小(约50×40微米),分支少于10个,占据单个层,并且不能根据轴突直径分为不同类别。对照成年鱼(体长6厘米)中染色的87个树突与之前检查的成年树突非常相似,来自细、中、粗轴突的树突范围分别平均为115、166和194微米,并有17至24个分支末端。12条频闪灯饲养的鱼的110个树突常常异常。虽然束状化正常,但束外路径异常,有反向转弯。轴突通常在其行程中有分支,并且这些分支分布在更广泛的范围内,而不是形成一个明显的簇。相比之下,任何一组中的分支数量和终止深度均未显著改变。粗直径的树突最异常,比对照组长64%,宽30%。细直径的树突也显著大了约20%,但中直径的树突没有扩大。(摘要截断于400字)

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