We have performed genetic linkage analysis in 13 large multiply affected families, to test the hypothesis that there is extensive heterogeneity of linkage for genetic subtypes of schizophrenia. Our strategy consisted of selecting 13 kindreds containing multiple affected cases in three or more generations, an absence of bipolar affective disorder, and a single progenitor source of schizophrenia with unilineal transmission into the branch of the kindred sampled. DNA samples from these families were genotyped with 365 microsatellite markers spaced at approximately 10-cM intervals across the whole genome. We observed LOD scores >3.0 at five distinct loci, either in the sample as a whole or within single families, strongly suggesting etiological heterogeneity. Heterogeneity LOD scores >3.0 in the sample as a whole were found at 1q33.2 (LOD score 3.2; P=.0003), 5q33.2 (LOD score 3.6; P=.0001), 8p22.1-22 (LOD score 3.6; P=.0001), and 11q21 (LOD score 3.1; P=.0004). LOD scores >3.0 within single pedigrees were found at 4q13-31 (LOD score 3.2; P=.0003) and at 11q23.3-24 (LOD score 3.2; P=.0003). A LOD score of 2.9 was also found at 20q12.1-11.23 within in a single family. The fact that other studies have also detected LOD scores >3.0 at 1q33.2, 5q33.2, 8p21-22 and 11q21 suggests that these regions do indeed harbor schizophrenia-susceptibility loci. We believe that the weight of evidence for linkage to the chromosome 1q22, 5q33.2, and 8p21-22 loci is now sufficient to justify intensive investigation of these regions by methods based on linkage disequilibrium. Such studies will soon allow the identification of mutations having a direct effect on susceptibility to schizophrenia.

In the feline visual system, neurons exhibiting sensitivity to the length of a moving contour were first observed in the cortex and described as 'hypercomplex cells'. In these cells an increase in stimulus length beyond an optimal value leads to a rapid decline in response. This decline has been attributed to an intracortical inhibitory input which may be driven by layer VI cells with very long receptive fields. It is now clear, however, that cells in the dorsal lateral geniculate nucleus (dLGN), exhibit a degree of length tuning similar to that of cortical 'hypercomplex cells', suggesting that this response property could be generated subcortically. Alternatively, as the dLGN receives a massive corticofugal projection from layer VI cells in the visual cortex, it is possible that this input has a function in generating length tuning in the dLGN. We have investigated this issue by comparing the length tuning of dLGN cells with and without corticofugal feedback. The data show that corticofugal feedback makes a highly significant contribution to the length tuning of dLGN cells. This raises the possibility that length tuning is an emergent property of the geniculo-cortical loop.

In a previous study, we have shown that the corticofugal projection to the dLGN enhances inhibitory mechanisms underlying length tuning. This suggests that the inhibitory influences deriving from the corticofugal feedback should exhibit characteristics that reflect the response properties of orientation-tuned layer VI cells. Here we report data obtained from experiments using a bipartite visual stimulus, with an inner section over the dLGN cell receptive field centre and an outer section extending beyond it. For both X and Y cells there was a modulation of the strength of the surround antagonism of centre responses that was dependent on the orientation alignment of contours in the two components of the stimulus. Layer VI cells showed maximal responses when the two components were aligned to the same orientation; dLGN cells showed a minimal response. Varying the orientation alignment of the inner and outer components of the stimulus in a randomised, interleaved fashion showed that bringing the stimulus into alignment resulted in a 24.28% increase in the surround antagonism of the centre response. Blocking cortical activity showed this effect of alignment to be strongly dependent on corticofugal feedback. This effect of orientation alignment appears to apply for any absolute orientation of the alignment condition and supports the view that an entire subset of cortical orientation columns generate the feedback influencing any given dLGN cell. This mechanism makes dLGN cells sensitive to the orientation domain discontinuities in elongated contours moving across their receptive field.

Two approaches were adopted to study the pattern of connectivity between the cat visual cortex and lateral geniculate nucleus. Fourteen individual cortico-geniculate axons were labeled and reconstructed after intracellular or extracellular injection of biocytin into regions of known receptive-field position and ocular dominance preference, and the distribution of boutons from multi-axon clusters was mapped in three dimensions and compared with the locations of strategically placed geniculate recordings made in the same tissue. The results show that the feedback has an accurate retinotopic component but that individual axons are both more extensive and more selective than described previously. Area 17 feedback axons terminate primarily in layers A and A1, but the distribution of terminal boutons is strongly biased (3:1 ratio) toward the layer that matches their eye preference. Thus, those driven by the contralateral eye preferentially target layer A, and those driven by the ipsilateral eye target layer A1. Each axon also innervates the perigeniculate nucleus (PGN), but the pattern is otherwise variable, suggesting that there are different axonal classes. The terminal fields of individual axons are much larger than described previously, with a maximum spread of 500-1500 microns. Nevertheless, the projection from a given location in area 17 has a center of maximum terminal density 400-500 microns across, which is in retinotopic correspondence with the aggregate receptive field of the cortical cells of origin. The surrounding zone of relatively sparse boutons, however, must permit corticofugal cells to influence visual processing well beyond the regions over which their own responses summate. It follows that any geniculate cell receives corticofugal input covering an equally extensive area of visual space.