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1.
Neuroscience ; 149(1): 87-98, 2007 Oct 12.
Article in English | MEDLINE | ID: mdl-17826919

ABSTRACT

Matrix metalloproteinase-7 (MMP-7) belongs to a family of zinc dependent endopeptidases that are expressed in a variety of tissues including the brain. MMPs are known to be potent mediators of pericellular proteolysis and likely mediators of dynamic remodelling of neuronal connections. While an association between proteases and the neuronal synapse is emerging, a full understanding of this relationship is lacking. Here, we show that MMP-7 alters the structure and function of presynaptic terminals without affecting neuronal survival. Bath application of recombinant MMP-7 to cultured rat neurons induced long-lasting inhibition of vesicular recycling as measured by synaptotagmin 1 antibody uptake assays and FM4-64 optical imaging. MMP-7 application resulted in reduced abundance of vesicular and active zone proteins locally within synaptic terminals although their general levels remained unaltered. Finally, chronic application of the protease resulted in synaptic atrophy, including smaller terminals and fewer synaptic vesicles, as determined by electron microscopy. Together these results suggest that MMP-7 is a potent modulator of synaptic vesicle recycling and synaptic ultrastructure and that elevated levels of the enzyme, as may occur with brain inflammation, may adversely influence neurotransmission.


Subject(s)
Matrix Metalloproteinase 7/pharmacology , Neurons/drug effects , Synapses/drug effects , Synapses/pathology , Synaptic Vesicles/drug effects , Animals , Atrophy , Cells, Cultured , Embryo, Mammalian , Gene Expression Regulation/drug effects , Hippocampus/cytology , Humans , Matrix Metalloproteinase 1/pharmacology , Microscopy, Immunoelectron/methods , Protein Transport/drug effects , Pyridinium Compounds , Quaternary Ammonium Compounds , Rats , Rats, Sprague-Dawley , Synaptic Vesicles/metabolism , Synaptic Vesicles/ultrastructure , Synaptophysin/metabolism , Synaptotagmin I/metabolism , Vesicle-Associated Membrane Protein 2/metabolism
2.
Sci STKE ; 2001(95): pe1, 2001 Aug 14.
Article in English | MEDLINE | ID: mdl-11752671

ABSTRACT

Early in development, synapses with glycine or gamma-aminobutyric acid (GABA)-gated chloride channels exhibit the ability to depolarize postsynaptic cells. As the synapses mature and the gradient of chloride ions across the cell membrane is altered, these neurotransmitters signal an inhibitory response, hyperpolarizing the membrane and decreasing neuronal excitability. Kriegstein and Owens discuss how GABA-stimulated up-regulation of the expression of the potassium chloride cotransporter KCC2 may be the mechanism underlying this synaptic switch.


Subject(s)
Nerve Growth Factors/physiology , Synapses/physiology , gamma-Aminobutyric Acid/physiology , Animals , Synaptic Transmission/physiology
4.
Dev Neurosci ; 22(1-2): 25-33, 2000.
Article in English | MEDLINE | ID: mdl-10657695

ABSTRACT

Cell-cell signaling within the neocortical ventricular zone (VZ) has been shown to influence the proliferation of VZ precursor cells and the subsequent differentiation and fate of postmitotic neurons. Calcium (Ca(2+)), a ubiquitous second messenger implicated in the regulation of many aspects of development, may play a role in these signaling events. Accordingly, we have examined the spatiotemporal patterns of spontaneous intracellular free Ca(2+) ([Ca(2+)](i)) fluctuations of cells within the intact neocortical VZ. Previous observations have demonstrated that similar patterns of spontaneous [Ca(2+)](i) increase occur in both proliferative and postmitotic cortical cells, suggesting that they may be mechanistically similar. Our results suggest that the changes in [Ca(2+)](i) in VZ cells and cortical plate neurons are likely triggered by different mechansims, and imply that similar changes in [Ca(2+)](i) may underlie different signaling events during distinct phases of neocortical development.


Subject(s)
Calcium/metabolism , Cerebral Ventricles/embryology , Neocortex/embryology , Neurons/metabolism , Animals , Cerebral Ventricles/cytology , Cycloleucine/analogs & derivatives , Cycloleucine/pharmacology , Embryo, Mammalian/metabolism , Embryonic and Fetal Development/physiology , Intracellular Membranes/metabolism , Mice , Neocortex/cytology , Neurons/drug effects , Osmolar Concentration , Rats , Rats, Sprague-Dawley , Receptors, Metabotropic Glutamate/agonists , Ryanodine Receptor Calcium Release Channel/physiology
6.
J Neurophysiol ; 82(2): 570-83, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10444657

ABSTRACT

Evidence from several brain regions suggests gamma-aminobutyric acid (GABA) can exert a trophic influence during development, expanding the role of this amino acid beyond its function as an inhibitory neurotransmitter. Proliferating precursor cells in the neocortical ventricular zone (VZ) express functional GABA(A) receptors as do immature postmigratory neurons in the developing cortical plate (CP); however, GABA(A) receptor properties in these distinct cell populations have not been compared. Using electrophysiological techniques in embryonic and early postnatal neocortex, we find that GABA(A) receptors expressed by VZ cells have a higher apparent affinity for GABA and are relatively insensitive to receptor desensitization compared with neurons in the CP. GABA-induced current magnitude increases with maturation with the smallest responses found in recordings from precursor cells in the VZ. No evidence was found that GABA(A) receptors on VZ cells are activated synaptically, consistent with previous data suggesting that these receptors are activated in a paracrine fashion by nonsynaptically released ligand. After neurons are born and migrate to the CP, they begin to demonstrate spontaneous synaptic activity, the majority of which is GABA(A) mediated. These spontaneous GABA(A) postsynaptic currents (sPSCs) first were detected at embryonic day 18 (E18). At birth, approximately 50% of recordings from cortical neurons demonstrated GABA(A)-mediated sPSCs, and this value increased with age. GABA(A)-mediated sPSCs were action potential dependent and arose from local GABAergic interneurons. GABA application could evoke action potential-dependent PSCs in neonatal cortical neurons, suggesting that during the first few postnatal days, GABA can act as an excitatory neurotransmitter. Finally, N-methyl-D-aspartate (NMDA)- but not non-NMDA-mediated sPSCs were also present in early postnatal neurons. These events were not observed in cells voltage clamped at negative holding potentials (-60 to -70 mV) but were evident when the holding potential was set at positive values (+30 to +60 mV). Together these results provide evidence for the early maturation of GABAergic communication in the neocortex and a functional change in GABA(A)-receptor properties between precursor cells and early postmitotic neurons. The change in GABA(A)-receptor properties may reflect the shift from paracrine to synaptic receptor activation.


Subject(s)
Neocortex/physiology , Receptors, GABA-A/physiology , Signal Transduction/physiology , Animals , Cell Division/physiology , Embryonic and Fetal Development/physiology , Mitosis/physiology , Neocortex/embryology , Neocortex/growth & development , Patch-Clamp Techniques , Rats , Rats, Sprague-Dawley , Synaptic Transmission/physiology
7.
J Neurosci ; 18(14): 5374-88, 1998 Jul 15.
Article in English | MEDLINE | ID: mdl-9651220

ABSTRACT

Changes in intracellular free calcium concentration ([Ca2+]i) are known to influence a variety of events in developing neurons. Although spontaneous changes of [Ca2+]i have been examined in immature cortical neurons, the calcium dynamics of cortical precursor cells have received less attention. Using an intact cortical mantle and confocal laser microscopy, we examined the spatiotemporal patterns of spontaneous [Ca2+]i fluctuations in neocortical ventricular zone (VZ) cells in situ. The majority of activity consisted of single cells that displayed independent [Ca2+]i fluctuations. These events occurred in cells throughout the depth of the VZ. Immunohistochemical staining confirmed that these events occurred primarily in precursor cells rather than in postmitotic neurons. When imaging near the ventricular surface, synchronous spontaneous [Ca2+]i increases were frequently observed in pairs of adjacent cells. Cellular morphology, time-lapse imaging, and nuclear staining demonstrated that this activity occurred in mitotically active cells. A third and infrequently encountered pattern of activity consisted of coordinated spontaneous increases in [Ca2+]i in groups of neighboring VZ cells. The morphological characteristics of these cells and immunohistochemical staining suggested that the coordinated events occurred in gap junction-coupled precursor cells. All three patterns of activity were dependent on the release of Ca2+ from intracellular stores. These results demonstrate distinct patterns of spontaneous [Ca2+]i change in cortical precursor cells and raise the possibility that these dynamics may contribute to the regulation of neurogenesis.


Subject(s)
Calcium/metabolism , Cerebral Ventricles/metabolism , Neurons/metabolism , Stem Cells/metabolism , Animals , Cellular Senescence/physiology , Cerebral Ventricles/cytology , Immunohistochemistry , In Vitro Techniques , Rats , Rats, Sprague-Dawley , Time Factors
8.
J Neurosci ; 17(18): 7037-44, 1997 Sep 15.
Article in English | MEDLINE | ID: mdl-9278539

ABSTRACT

Cells within the ventricular zone (VZ) of developing neocortex are coupled together into clusters by gap junction channels. The specific role of clustering in cortical neurogenesis is unknown; however, clustering provides a means for spatially restricted local interactions between subsets of precursors and other cells within the VZ. In the present study, we have used a combination of 5-bromo-2'-deoxyuridine (BrDU) pulse labeling, intracellular biocytin labeling, and immunocytochemistry to determine when in the cell cycle VZ cells couple and uncouple from clusters and to determine what cell types within the VZ are coupled to clusters. Our results indicate that clusters contain radial glia and neural precursors but do not contain differentiating or migrating neurons. In early neurogenesis, all precursors in S and G2 phases of the cell cycle are coupled, and approximately half of the cells in G1 are coupled. In late neurogenesis, however, over half of the cells in both G1 and S phases are not coupled to VZ clusters, whereas all cells in G2 are coupled to clusters. Increased uncoupling in S phase during late neurogenesis may contribute to the greater percentage of VZ cells exiting the cell cycle at this time. Consistent with this hypothesis, we found that pharmacologically uncoupling VZ cells with octanol decreases the percentage of VZ cells that enter S phase. These results demonstrate that cell clustering in the VZ is restricted to neural precursors and radial glia, is dynamic through the cell cycle, and may play a role in regulating neurogenesis.


Subject(s)
Cell Communication/physiology , Cerebral Cortex/embryology , Cerebral Ventricles/embryology , Animals , Bromodeoxyuridine/metabolism , Cell Cycle , Cerebral Cortex/cytology , Cerebral Ventricles/cytology , Epithelial Cells , Female , G1 Phase , G2 Phase , Gap Junctions/metabolism , Lysine/analogs & derivatives , Lysine/metabolism , Mice , Pregnancy , S Phase , Tubulin/analysis
9.
J Neurosci ; 16(20): 6414-23, 1996 Oct 15.
Article in English | MEDLINE | ID: mdl-8815920

ABSTRACT

Gramicidin perforated-patch-clamp recordings in brain slices were used to obtain an accurate assessment of the developmental change in the GABAA receptor reversal potential (EGABAA) in embryonic and early postnatal rat neocortical cells including neuroepithelial precursor cells, cortical plate neurons, and postnatal neocortical neurons. Our results demonstrate that there is a progressive negative shift in EGABAA with the most positive values found in the youngest cortical precursor cells. At the early stages of neocortical development, EGABAA is determined by the chloride (Cl-) gradient, and the internal chloride concentration ([Cl-]i) decreases with development. EGABAA is positive to the resting potential, indicating that GABA serves to depolarize developing neocortical cells. Consistent with this conclusion, GABAA receptor activation with muscimol was found-to increase the internal calcium concentration ([Ca2+]i) in both embryonic and early postnatal neocortical cells through the activation of voltage-gated calcium channels (VGCCs). Postnatal cells exhibit spontaneous postsynaptic synaptic currents, which are eliminated by bicuculline methiodide (BMI) but not glutamate receptor antagonists and reverse at the Cl- equilibrium potential. Likewise, brief spontaneous increases in [Ca2+]i, sensitive to BMI and TTX, are observed at the same ages, suggesting that endogenous synaptic GABAA receptor activation can depolarize cells and activate VGCCs. These results suggest that GABAA receptor-mediated depolarization may influence early neocortical developmental events, including neurogenesis and synaptogenesis, through the activation of Ca(2+)-dependent signal transduction pathways.


Subject(s)
Calcium/metabolism , Cerebral Cortex/growth & development , Receptors, GABA/physiology , gamma-Aminobutyric Acid/pharmacology , Animals , Animals, Newborn/metabolism , Cerebral Cortex/drug effects , Gramicidin/pharmacology , Muscimol/pharmacology , Patch-Clamp Techniques , Rats , Rats, Sprague-Dawley , Time Factors
10.
Neuron ; 15(6): 1287-98, 1995 Dec.
Article in English | MEDLINE | ID: mdl-8845153

ABSTRACT

We have found that, during the early stages of cortical neurogenesis, both GABA and glutamate depolarize cells in the ventricular zone of rat embryonic neocortex. In the ventricular zone, glutamate acts on AMPA/kainate receptors, while GABA acts on GABAA receptors. GABA induces an inward current at resting membrane potentials, presumably owing to a high intracellular Cl- concentration maintained by furosemide-sensitive Cl- transport. GABA and glutamate also produce increases in intracellular Ca2+ in ventricular zone cells, in part through activation of voltage-gated Ca2+ channels. Furthermore, GABA and glutamate decrease the number of embryonic cortical cells synthesizing DNA. Depolarization with K+ similarly decreases DNA synthesis, suggesting that the neurotransmitters act via membrane depolarization. Applied alone, GABAA and AMPA/kainate receptor antagonists increase DNA synthesis, indicating that endogenously released amino acids influence neocortical progenitors in the cell cycle. These results demonstrate a novel role for amino acid neurotransmitters in regulating neocortical neurogenesis.


Subject(s)
Cerebral Cortex/cytology , DNA/biosynthesis , Glutamic Acid/pharmacology , Stem Cells/drug effects , Stem Cells/metabolism , gamma-Aminobutyric Acid/pharmacology , Animals , Cell Polarity/drug effects , Cerebral Cortex/embryology , Cerebral Cortex/metabolism , Patch-Clamp Techniques , Rats , Rats, Sprague-Dawley
11.
Neuron ; 9(3): 505-13, 1992 Sep.
Article in English | MEDLINE | ID: mdl-1524828

ABSTRACT

The neuroendocrine bag cell neurons of the marine mollusk Aplysia produce prolonged inhibition that lasts for more than 2 hr. We purified a peptide from the abdominal ganglion that mimics this inhibition. Mass spectrometry and microsequence analysis indicate that the peptide is 40 aa long and is amidated at its carboxyl terminus. It is highly homologous to vertebrate neuropeptide Y (NPY) and other members of the pancreatic polypeptide family. As determined from cloned cDNA, the gene coding for the precursor protein shares a common structural organization with genes encoding precursors of the vertebrate family. The peptides may therefore have arisen from a common ancestral gene. Bag cell neurons are immunoreactive for Aplysia NPY, and Northern blot analysis indicates that as with its vertebrate counterparts, the peptide is abundantly expressed in the CNS. This suggests that peptides related to NPY may have important functions in the nervous system of Aplysia as well as in other invertebrates.


Subject(s)
Aplysia/metabolism , Cloning, Molecular , Neural Inhibition , Neurons/drug effects , Neuropeptide Y/genetics , Neuropeptides/pharmacology , Sequence Homology, Nucleic Acid , Amino Acid Sequence , Animals , Base Sequence , Immunohistochemistry , Invertebrate Hormones/metabolism , Molecular Sequence Data , Neurons/physiology , Neuropeptide Y/metabolism , Neuropeptides/genetics , Protein Precursors/chemistry , Protein Precursors/metabolism , Vertebrates/metabolism
12.
J Neurobiol ; 23(6): 656-70, 1992 Aug.
Article in English | MEDLINE | ID: mdl-1359004

ABSTRACT

Alpha-bag cell peptide [alpha-BCP (Ala-Pro-Arg-Leu-Arg-Phe-Tyr-Ser-Leu)] is a neurotransmitter that mediates bag cell-induced inhibition of left-upper-quadrant (LUQ) neurons L2, L3, L4, and L6 in the abdominal ganglion of Aplysia. Our recent biochemical studies have shown that alpha-BCP[1-9] is cleaved into alpha-BCP[1-2], [3-9], [1-5], [6-9], and [7-9] by a combination of three distinct peptidase activities located within the extracellular spaces of the CNS: A diaminopeptidase-IV (DAP-IV)-like enzyme cleaves alpha-BCP[1-9] at the 2-3 peptide bond; a neutral metalloendopeptidase (NEP)-like enzyme cleaves either alpha-BCP[1-9] or alpha-BCP[3-9] at the 5-6 bond; an aminopeptidase M-II (APM-II)-like enzyme cleaves alpha-BCP[6-9] at the 6-7 bond, but cleaves neither alpha-BCP[1-9], nor the other ganglionic peptidase products. To further understand the manner in which alpha-BCP is inactivated after release, that is loses its electrophysiological activity, we studied its structure-activity relationship by recording intracellularly from LUQ neurons in isolated abdominal ganglia that were arterially perfused with peptides dissolved in artificial sea water. The effects of alpha-BCP[1-9] and 15 of its fragments ([1-8], [1-7], [1-6], [1-5], [2-9], [3-9], [3-8], [6-9], [7-9], [8-9], [6-7], [6-8], [1-2], Phe, Tyr) indicated that the sequence Phe6-Tyr7 was both necessary and sufficient to produce LUQ inhibitory activity.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Aplysia/physiology , Extracellular Space/metabolism , Neurons/physiology , Neurotransmitter Agents/physiology , Oligopeptides/physiology , Action Potentials , Amino Acid Sequence , Animals , Chromatography, High Pressure Liquid , Electrophysiology , Eye/innervation , Ganglia/cytology , Molecular Sequence Data , Ocular Physiological Phenomena , Structure-Activity Relationship
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