Horton J C, Hocking D R
Beckman Vision Center, University of California, San Francisco, San Francisco, California 94143-0730, USA.
J Neurosci. 1997 May 15;17(10):3684-709. doi: 10.1523/JNEUROSCI.17-10-03684.1997.
Visual deprivation induced by monocular eyelid suture, a laboratory model for congenital cataract, results in shrinkage of ocular dominance columns serving the closed eye. We performed monocular suture in macaques at ages 1, 3, 5, 7, and 12 weeks to define the critical period for plasticity of ocular dominance columns. After a minimum survival of 8 months, complete montages of [3H]proline-labeled columns were reconstructed from flat-mounts of striate cortex in both hemispheres. In any given monkey, visual deprivation induced the columns throughout striate cortex (V1) to retract the same distance from their original borders in layer IVcbeta. After deprivation, the widest columns remained in the foveal representation and along the V1/V2 border, where columns are widest in control animals. The narrowest deprived columns belonged to the ipsilateral eye, especially along the horizontal meridian and in the periphery, where columns are narrowest in control animals. At the earliest age that we tested (1 week), visual deprivation reduced the columns to fragments. These fragments always coincided with a cytochrome oxidase patch, or a short string of patches, in the upper layers. More severe column shrinkage occurred in layer IVcbeta (parvo) than layer IVcalpha (magno). The geniculate input to the patches in layer III (konio) appeared normal after deprivation, despite loss of CO activity. Surprisingly, the blind spot representation of the open eye was shrunken by monocular deprivation, although binocular competition is absent in this region. Our principal finding was that eyelid suture at age 1 week caused the most severe column shrinkage. With suture at later ages, the degree of column shrinkage showed a progressive decline. Deprivation commencing at age 12 weeks caused no column shrinkage. These results imply that primate visual cortex is most vulnerable to deprivation during the first weeks of life. Our experiments should provide further impetus for the treatment of children with congenital cataract at the earliest possible age.
单眼眼睑缝合诱导的视觉剥夺是先天性白内障的一种实验室模型,会导致为闭眼服务的眼优势柱缩小。我们在1、3、5、7和12周龄的猕猴身上进行单眼缝合,以确定眼优势柱可塑性的关键期。在至少存活8个月后,从两个半球纹状皮层的平展标本中重建了完整的[³H]脯氨酸标记柱蒙太奇图像。在任何给定的猴子中,视觉剥夺导致整个纹状皮层(V1)的柱从其在IVcβ层的原始边界缩回相同的距离。剥夺后,最宽的柱保留在中央凹代表区以及V1/V2边界沿线,在对照动物中这些区域的柱最宽。最窄的剥夺柱属于同侧眼,尤其是沿水平子午线和周边区域,在对照动物中这些区域的柱最窄。在我们测试的最早年龄(1周),视觉剥夺使柱缩小为碎片。这些碎片总是与上层的细胞色素氧化酶斑或一小串斑重合。IVcβ层(小细胞)比IVα层(大细胞)发生更严重的柱收缩。尽管CO活性丧失,但剥夺后III层(侏儒细胞)中斑的膝状体输入看起来正常。令人惊讶的是,尽管该区域不存在双眼竞争,但单眼剥夺会使睁眼的盲点代表区缩小。我们的主要发现是,1周龄时的眼睑缝合导致最严重的柱收缩。随着缝合年龄的增加,柱收缩程度逐渐下降。12周龄开始的剥夺未导致柱收缩。这些结果表明,灵长类动物视觉皮层在生命的最初几周对剥夺最敏感。我们的实验应该为尽早治疗先天性白内障儿童提供进一步的动力。