Cellular and molecular signals involved in axon elongation versus collateral and arbor formation may be intrinsic to developing neurons, or they may derive from targets. To identify signals regulating axon growth modes, we have developed a culture system in which trigeminal ganglion cells are challenged by various target tissues. Embryonic day 15 (E15) rat trigeminal ganglion explants were placed between peripheral (vibrissa pad) and central nervous system targets. Normally, bipolar trigeminal ganglion cells extend one process to the vibrissa pad and another to the brainstem trigeminal complex. Under coculture conditions, the peripheral processes invade the vibrissa pad explants and form a characteristic circumfollicular pattern. Central processes of E15 ganglion cells invade many, but not all, central nervous system tissues. In isochronic (E15) central nervous system explants such as brainstem, olfactory bulb, or neocortex, these central processes elongate and form a "tract" but have virtually no arbors. However, in more mature targets (e.g., a section from postnatal brainstem or neocortex), they form arbors instead of a tract. We conclude from these observations that whether trigeminal axons elongate to form a tract, or whether they begin to arborize, is dictated by the target tissue and not by an intrinsic developmental program of the ganglion cell body. The explant coculture system is an excellent model for analysis of the molecular basis of neuron-target interactions.Nocturnal rodents acquire much information about their environment through a chain of neuronal assemblies that bridges the whiskers and the cerebral cortex (1). Neocortical cells receiving this information are organized into modules or "barrels" whose distribution reflects the spatial organization of the whiskers; equivalent patterns of neuronal projection are found in the trigeminal regions ofbrainstem and thalamus (1). Neurons of the trigeminal ganglion constitute the first level of this pathway. They have peripheral and central processes that project to the whisker pad and brainstem, respectively. Brainstem afferent terminations are clustered in relation to a corresponding arrangement of postsynaptic neurons ("barrelettes"), which reflects the arrangement of whiskers on the snout (1). Because of the point-to-point representation of the vibrissae along the trigeminal neuraxis, this system has provided a model for investigations of axontarget interactions in the formation of sensory maps in the brain (1).During development, axons exhibit two distinct growth modes. Initially they elongate, without branching, toward their target and form a tract (2-8). Next, parent axons in the tract emit collaterals, which penetrate target zones and form arbors therein; as development proceeds, some collaterals are eliminated, whereas others are elaborated. These two major modes of axon growth, elongation and collateral/arborThe publication costs of this article were defrayed in part by page charge payment. This article must therefore be hereby marked "...