The cellular distribution of the type 3 serotonin receptor (5HT 3 R) in the rat brain was established immunocytochemically by using a polyclonal antibody raised against a synthetic peptide from the deduced amino-acid sequence of the cloned 5HT 3 R. The 5HT 3 Rimmunoreactive neurons were found in the
Developmental shift in expression of netrin receptors in the rat spinal cord: Predominance of UNC-5 homologues in adulthood
β Scribed by Colleen Manitt; Katherine M. Thompson; Timothy E. Kennedy
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 394 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0360-4012
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β¦ Synopsis
Abstract
Netrins are a family of secreted proteins required for normal neural development. Netrinβ1 is expressed at similar levels in the adult rat spinal cord and the embryonic CNS, suggesting that it contributes to adult CNS function. Here we show that the netrin receptors dcc, neogenin, unc5h1, unc5h2, and unc5h3 are also expressed in the adult rat spinal cord. Lower levels of DCC and neogenin were detected in the adult relative to the embryonic CNS. Conversely, the adult spinal cord contains increased levels of UNCβ5 homologues in comparison with the embryo. Multiple mRNA transcripts detected by Northern blot analysis suggested that netrin receptors might be encoded by alternatively spliced mRNAs. We have identified a novel alternatively spliced mRNA encoding UNC5H1, UNC5H1^Ξ^TSP1, which lacks the first of the two extracellular thrombospondin domains. This novel splice variant is the major transcript detected in the early embryonic CNS, although both splice variants are expressed in the adult. Previously identified alternatively spliced mRNAs encoding DCC and neogenin were also detected. Dcc, neogenin, unc5h1, unc5h2, and unc5h3 are expressed by subsets of neurons. Robust expression of unc5h2 was found in glia. These findings suggest that uncβ5 homologues constitute a major mode of netrinβ1 signal transduction in the adult spinal cord and may be involved in phenomena analogous to axon repulsion, such as inhibiting process extension and collateral sprouting. Β© 2004 WileyβLiss, Inc.
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