Nerve axons in the central and peripheral nervous system are normally surrounded by satellite cells. These cells, known as Schwann cells in the peripheral nervous system, interact with axons to form a myelin sheath, so allowing nerve impulses to proceed at high speed. Schwann cells are thought to differ from neurones in their membrane properties in one important aspect: they lack excitability. Using the patch-clamp technique we have now measured directly the ionic currents across the membrane of single Schwann cells cultured from newborn rabbits. Surprisingly, we found that these Schwann cells possess voltage-gated sodium and potassium channels that are similar to those present in neuronal membranes.
Population response of [Ca2+]i in cultured cortical astrocytes to excitatory amino acids was measured at room temperature using the calcium-sensitive dye fura-2. Quisqualic acid (QA), glutamate (Glu), and kainic acid (KA) caused a peak increase in [Ca2+]i in the order QA greater than Glu greater than KA. No response to N-methyl-D-aspartic acid (NMDA) was observed whether or not Mg2+ was present externally. Both QA and Glu (100 microM) frequently elicited a decaying oscillatory [Ca2+]i response during sustained agonist application; the period of oscillations initially was 23.5 sec and increased as the response was damped. Comparatively, the [Ca2+]i response to KA was nonoscillatory. Both responses to Glu and KA were reduced slightly by antagonist gamma- D-glutamylaminomethyl-sulfonic acid (1 mM), but virtually were abolished by kynurenic acid (3 mM). Replacement of external Na+ by choline had no significant effect on the Glu response. Removal of external Ca2+ reduced the peak response to QA, Glu, and KA to 40, 34, and 18%, respectively; and markedly reduced the degree of QA- and Glu- induced [Ca2+]i oscillations. Pretreatment with phorbol esters, a potent activator of protein kinase C, blocked the [Ca2+]i response to Glu but not KA. It is concluded that cortical astrocytes express Glu receptors of the non-NMDA type in culture and that receptor activation leads to Ca2+ influx and release of internal Ca2+. Mobilization of Ca2+ apparently occurs via the known Glu-mediated hydrolysis of inositol lipids, which may come under negative-feed-back control by protein kinase C activation. Oscillatory [Ca2+]i signaling offers the possibility of a dynamic population response in an electrically coupled glial network.
Genetic analysis in mice has revealed a key genetic pathway, SUMO-specific protease 2 (SENP2)-Mdm2-p53, essential for trophoblast development. Targeted disruption of SENP2 impairs the G-S transition required for mitotic and endoreduplication cell cycles during the expansion of trophoblast stem cells and their differentiation into polyploidy cells, respectively. The disruption disturbed the subcellular distribution and SUMO modification of Mdm2, leading to interference with p53 degradation. Here, we further explore the mechanism underlying SENP2-mediated regulation of Mdm2 in p53-induced cellular stress. We identify a specific isoform of SENP2 necessary and sufficient to negatively regulate the p53-dependent transcription and its related stress responses. This isoform-specific effect is attributed to the differential compartmentalization of SENP2. SUMO conjugation of Mdm2 induces its co-localization and association with SENP2 in promyelocytic leukemia bodies. Biochemical studies show that SENP2 catalyzes the desumoylation process of Mdm2. SENP2-dependent regulation of Mdm2 is sensitive to its p53-binding activity. Our findings led us to propose a mechanism underlying the SENP2-mediated regulation of Mdm2 that is critical for genome integrity in p53-dependent stress responses. Cell Death and Differentiation (2011) 18, 1005-1015; doi:10.1038/cdd.2010.168; published online 24 December 2010Small ubiquitin-related modifier (SUMO, also known as sentrin) is a member of the ubiquitin-like modifier family. 1 This covalent conjugation process is reversible and highly evolutionarily conserved among species. 2 SUMO functions in a manner similar to ubiquitin, where it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitination with a well-established role in targeting protein degradation, SUMO modification is involved in a variety of cellular processes, including protein trafficking, transcriptional regulation, cell survival and death, and protein stability. 3 Many sumoylated proteins have been shown to preferentially accumulate in specific complexes such as the nuclear pore and promyelocytic leukemia (PML) bodies. 4,5 Similar to ubiquitination, sumoylation requires processing, conjugation and transfer. The transfer process, which covalently conjugates SUMO polypeptides to their targets, is catalyzed by E3 ligases. 6 The reverse desumoylation process is mediated by SUMO-specific proteases (SENPs). Although SENPs have been linked to catalyze SUMO modification in various physiological systems, their roles in mammalian development and pathogenesis remain largely elusive.We previously demonstrated that SENP2 is essential for modulating the p53/Mdm2 circuit in trophoblast development. 7 Targeted disruption of SENP2 in mice impaired the G-S transition required for mitotic and endoreduplication cell cycles during expansion of trophoblast stem (TS) cells and their differentiation into polyploid cells, respectively. 7 The SENP2 ablation apparently disturbed the subcellular distributi...
We have identified the glutamate receptor genes expressed by developing and adult rat optic nerve. Results from PCR suggested that of the ionotropic glutamate receptor (GluR) gene family, only GluR1 and GluR3 subunits are expressed by optic nerve. However, Northern blot analysis demonstrated that only the GluR1 subtype is expressed at appreciable levels. In situ hybridization histochemistry of GluR1 was performed and a diffuse pattern of expression was observed in both postnatal day 15 and adult optic nerve. Restriction mapping of the GluR1 PCR product indicated the expression of the flip alternative splice version in optic nerve. The detected GluR1 message was not due to axons because no loss of expression was observed after the degeneration of axons. PCR analysis also revealed the presence of a metabotropic glutamate receptor in optic nerve.
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