“…Since the 1980s, with the advent of immunohistochemical strategies for identifying cell types, researcher had begun correlating cell-specific neurochemical marker expression (typically Ca 2+ -binding proteins, neuropeptides and certain receptors) with morphological and electrophysiological characterization in order to distinguish several subtypes of GABAergic interneurons (Kubota et al, 1993, 2011; Kubota and Kawaguchi, 1994, 1997; Cauli et al, 2014). Recent advances suggest that neurons expressing an unidentified cytoplasmic antigen Rat-303 (Hockfield, 1987; Hockberger et al, 1994; Geurts et al, 2001), the metabotropic glutamate and serotonin receptors (Neki et al, 1996; Geurts et al, 2001, 2002; Simat et al, 2007; Sillitoe et al, 2008), the neuropeptide somatostatin (SOM; Johansson et al, 1984; Geurts et al, 2001; Galas et al, 2017) and Ca 2+ -binding proteins such as parvalbumin and calretinin, respectively (PRV and CRT; Schneeberger et al, 1985; Rogers, 1989; Geurts et al, 2001; Schwaller et al, 2002; Bastianelli, 2003; Pibiri et al, 2017), account for nearly 100% of cerebellar GABAergic interneurons. Rat-303 antibody selectively stains Golgi cells and LCs (Hockfield, 1987; Rogers, 1989; Dieudonné and Dumoulin, 2000; Geurts et al, 2001, 2002).…”