Role of α7 Nicotinic Acetylcholine Receptor in Calcium Signaling Induced by Prion Protein Interaction with Stress-inducible Protein 1*

The prion protein (PrPC) is a conserved glycosylphosphatidylinositol-anchored cell surface protein expressed by neurons and other cells. Stress-inducible protein 1 (STI1) binds PrPC extracellularly, and this activated signaling complex promotes neuronal differentiation and neuroprotection via the extracellular signal-regulated kinase 1 and 2 (ERK1/2) and cAMP-dependent protein kinase 1 (PKA) pathways. However, the mechanism by which the PrPC-STI1 interaction transduces extracellular signals to the intracellular environment is unknown. We found that in hippocampal neurons, STI1-PrPC engagement induces an increase in intracellular Ca2+ levels. This effect was not detected in PrPC-null neurons or wild-type neurons treated with an STI1 mutant unable to bind PrPC. Using a best candidate approach to test for potential channels involved in Ca2+ influx evoked by STI1-PrPC, we found that α-bungarotoxin, a specific inhibitor for α7 nicotinic acetylcholine receptor (α7nAChR), was able to block PrPC-STI1-mediated signaling, neuroprotection, and neuritogenesis. Importantly, when α7nAChR was transfected into HEK 293 cells, it formed a functional complex with PrPC and allowed reconstitution of signaling by PrPC-STI1 interaction. These results indicate that STI1 can interact with the PrPC·α7nAChR complex to promote signaling and provide a novel potential target for modulation of the effects of prion protein in neurodegenerative diseases

A new Aspidoras (Siluriformes: Callichthyidae) from rio Paraguaçu basin, Chapada Diamantina, Bahia, Brazil

During a recent ichthyological survey in Chapada Diamantina, Estado da Bahia, Brazil, a new, very distinctive Aspidoras was discovered in tributaries of the upper rio Paraguaçu. The new taxon differs from its congeners mainly in having: a poorly-developed pigmentation pattern, restricted to minute scattered blotches on dorsal region of head and body, but grouped in small, irregular blotches along the lateral body plate junction; four or five caudal vertebra, anterior to compound caudal centrum, with neural and haemal spines placed posteriorly, close to post-zygapophyses; and post-zygapophyses of the precaudal vertebrae without dorsal expansions connected with their respective neural spines. The new species shares with Aspidoras velites dorsolateral body plates not touching their counterparts dorsally, and infraorbital bones with reduced flanges that are restricted to the latero-sensory canal. Both of these are considered reductive character states, probably indicating a paedomorphic condition to both species. The new species is also compared to Aspidoras maculosus, a congener which bears the most similar color pattern and is geographically closest to the new species