نبذة مختصرة : Reeler heterozygous mice (reln(+/-)) are seemingly normal but haplodeficient in reln, a gene implicated in autism. Structural/neurochemical alterations in the reln(+/-) brain are subtle and difficult to demonstrate. Therefore, the usefulness of these mice in translational research is still debated. As evidence implicated several synapse-related genes in autism and the cerebellar vermis is structurally altered in the condition, we have investigated the expression of synaptophysin 1 (SYP1) and contactin 6 (CNTN6) within the vermis of reln(+/-) mice. Semi-thin plastic sections of the vermis from adult mice of both sexes and different genotypes (reln(+/-) and reln(+/+)) were processed with an indirect immunofluorescence protocol. Immunofluorescence was quantified on binary images and statistically analyzed. Reln(+/-) males displayed a statistically significant reduction of 11.89% in the expression of SYP1 compared to sex-matched wild-type animals, whereas no differences were observed between reln(+/+) and reln(+/-) females. In reln(+/-) male mice, reductions were particularly evident in the molecular layer: 10.23% less SYP1 than reln(+/+) males and 5.84%
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