Expression of a synapse‐associated membrane protein, P84/SHPS‐1, and its ligand, IAP/CD47, in mouse retina
ZP Mi, P Jiang, WL Weng, FP Lindberg… - Journal of …, 2000 - Wiley Online Library
ZP Mi, P Jiang, WL Weng, FP Lindberg, V Narayanan, CF Lagenaur
Journal of Comparative Neurology, 2000•Wiley Online LibraryP84 and integrin associated protein (IAP) are heterophilic binding partners that are
expressed in the central nervous system in addition to a variety of other tissues. Both
molecules are known to be involved in cell signaling in nonneural tissues. In the retina, both
molecules are expressed prominently in plexiform layers, suggesting a possible association
with synapses. Here, we examined the cellular expression and ultrastructural localization of
the two molecules in the developing mouse retina. Both appeared to be expressed at one or …
expressed in the central nervous system in addition to a variety of other tissues. Both
molecules are known to be involved in cell signaling in nonneural tissues. In the retina, both
molecules are expressed prominently in plexiform layers, suggesting a possible association
with synapses. Here, we examined the cellular expression and ultrastructural localization of
the two molecules in the developing mouse retina. Both appeared to be expressed at one or …
Abstract
P84 and integrin associated protein (IAP) are heterophilic binding partners that are expressed in the central nervous system in addition to a variety of other tissues. Both molecules are known to be involved in cell signaling in nonneural tissues. In the retina, both molecules are expressed prominently in plexiform layers, suggesting a possible association with synapses. Here, we examined the cellular expression and ultrastructural localization of the two molecules in the developing mouse retina. Both appeared to be expressed at one or both sides of synaptic sites, although the expression of IAP in the retina precedes that of P84. Examination of transgenic IAP‐null retinae revealed a failure of P84 to become associated with synaptic sites, suggesting the interaction of P84 with IAP was necessary for P84's synaptic localization. These findings suggest that the signaling activities of P84 and IAP are localized to sites of synaptic contact in the retina. Thus this pair of synapse‐associated molecules represents a bidirectional signaling system that could function to modify synaptic activity or possibly trophic interactions between central neurons. J. Comp. Neurol. 416:335–344, 2000. © 2000 Wiley‐Liss, Inc.
