Laminar and columnar distribution of geniculo‐cortical fibers in the macaque monkey

Abstract Single cell recordings in monkey striate cortex have shown differences in response properties from one cell layer to the next and have also shown that the IVth layer, which receives most of its input from the geniculate, is subdivided into a mosaic of regions, some connected to the left eye, others to the right. In the present study small lesions were made in single layers or pairs of layers in the lateral geniculate body, and the striate cortex was later examined with a Fink‐Heimer modification of the Nauta method. We hoped to correlate the laminar distribution of axon terminals in the cortex with functional differences between layers, and to demonstrate the IVth‐layer mosaic anatomically. After lesions in either of the two most dorsal (parvocellular) layers, terminal degeneration was found mainly in layer IVc, with a second minor input to a narrow band in the upper part of IVa. A very few degenerating fibers ascended to layer I. In contrast, lesions in either of the two ventral (magnocellular) layers were followed by terminal degeneration confined, apparently, to IVb, or at times extending for a short distance into the upper part of IVc; no degeneration was seen in layer IVa or in layer I. After a lesion confined to a single geniculate layer, a section through the corresponding region of striate cortex showed discrete areas or bands of degeneration in layer IV, usually 0.5–1.0 mm long, separated by interbands of about the same extent in which there was no terminal degeneration. When serial sections were reconstructed to obtain a face‐on view of the layer‐IV mosaic, it appeared as a series of regular, parallel, alternating degeneration‐rich and degeneration‐poor stripes. When a geniculate lesion involved both layer VI (the most dorsal, with input from the contralateral eye) and the part of layer V directly below (ipsilateral eye), the cortical degeneration, as expected, occupied a virtually continuous strip in layer IVc and the reconstructed face‐on view of this layer showed a large confluent region of degeneration. In some of the reconstructions the cortical stripes seemed highly regular; in others there was a variable amount of cross connection between stripes. The stripes varied in width from 0.25 to 0.50 mm, and width did not seem to correlate with region of retinal representation. It is concluded that the long narrow stripes of alternating left‐eye and right‐eye input to layer IV are an anatomical counterpart of the physiologically observed ocular‐dominance columns. Because of this segregation of inputs, cells of layer IV are almost invariably influenced by one eye only. A cell above or below layer IV will be dominated by the eye supplying the nearest IVth layer stripe, but will generally, though not always, receive a subsidiary input from the other eye, presumably by diagonal connections from the nearest stripes supplied by that eye.