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Merck
  • Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.

Peripheral nervous system genes expressed in central neurons induce growth on inhibitory substrates.

PloS one (2012-06-16)
William J Buchser, Robin P Smith, Jose R Pardinas, Candace L Haddox, Thomas Hutson, Lawrence Moon, Stanley R Hoffman, John L Bixby, Vance P Lemmon
摘要

Trauma to the spinal cord and brain can result in irreparable loss of function. This failure of recovery is in part due to inhibition of axon regeneration by myelin and chondroitin sulfate proteoglycans (CSPGs). Peripheral nervous system (PNS) neurons exhibit increased regenerative ability compared to central nervous system neurons, even in the presence of inhibitory environments. Previously, we identified over a thousand genes differentially expressed in PNS neurons relative to CNS neurons. These genes represent intrinsic differences that may account for the PNS's enhanced regenerative ability. Cerebellar neurons were transfected with cDNAs for each of these PNS genes to assess their ability to enhance neurite growth on inhibitory (CSPG) or permissive (laminin) substrates. Using high content analysis, we evaluated the phenotypic profile of each neuron to extract meaningful data for over 1100 genes. Several known growth associated proteins potentiated neurite growth on laminin. Most interestingly, novel genes were identified that promoted neurite growth on CSPGs (GPX3, EIF2B5, RBMX). Bioinformatic approaches also uncovered a number of novel gene families that altered neurite growth of CNS neurons.

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脱铁转铁蛋白 人, powder, BioReagent, suitable for cell culture, ≥98% (agarose gel electrophoresis)
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亚硒酸钠, BioReagent, suitable for cell culture, ≥98%
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聚-D-赖氨酸 氢溴酸盐, mol wt 30,000-70,000
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牛血清白蛋白 来源于牛血清, lyophilized powder, essentially globulin free, BioReagent, suitable for cell culture
Sigma-Aldrich
Gö 6976, Gö 6976, CAS 136194-77-9, is a cell-permeable, reversible, and ATP-competitive inhibitor of PKC (IC₅₀ = 7.9 nM for rat brain). Exhibits selectively for PKCα (IC₅₀ = 2.3 nM) and βI (IC₅₀ = 6.2 nM).