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1.
Neuroscience ; 146(1): 463-70, 2007 Apr 25.
Article in English | MEDLINE | ID: mdl-17320295

ABSTRACT

We used electron microscopy to determine the relative numbers of the three synaptic terminal types, RL (round vesicle, large terminal), RS (round vesicles, small terminal), and F (flattened vesicles), found in several representative thalamic nuclei in cats chosen as representative examples of first and higher order thalamic nuclei, where the first order nuclei relay subcortical information mainly to primary sensory cortex, and the higher order nuclei largely relay information from one cortical area to another. The nuclei sampled were the first order ventral posterior nucleus (somatosensory) and the ventral portion of the medial geniculate nucleus (auditory), and the higher order posterior nucleus (somatosensory) and the medial portion of the medial geniculate nucleus (auditory). We found that the relative percentage of synapses from RL terminals varied significantly among these nuclei, these values being higher for first order nuclei (12.6% for the ventral posterior nucleus and 8.2% for the ventral portion of the medial geniculate nucleus) than for the higher order nuclei (5.4% for the posterior nucleus, and 3.5% for the medial portion of the medial geniculate nucleus). This is consistent with a similar analysis of first and higher order nuclei for the visual system (the lateral geniculate nucleus and pulvinar, respectively). Since synapses from RL terminals represent the main information to be relayed, whereas synapses from F and RS terminals are modulatory in function, we conclude that there is relatively more modulation of the thalamic relay in the cortico-thalamo-cortical higher order pathway than in first order relays.


Subject(s)
Neural Pathways/anatomy & histology , Neurons/ultrastructure , Synapses/physiology , Thalamus/cytology , Animals , Cats , Microscopy, Electron, Transmission/methods , Microscopy, Immunoelectron/methods , Neurons/metabolism , Synapses/ultrastructure , gamma-Aminobutyric Acid/metabolism
2.
J Comp Neurol ; 440(4): 321-41, 2001 Nov 26.
Article in English | MEDLINE | ID: mdl-11745627

ABSTRACT

A major inhibitory input to the dorsal thalamus arises from neurons in the thalamic reticular nucleus (TRN), which use gamma-aminobutyric acid (GABA) as a neurotransmitter. We examined the synaptic targets of TRN terminals in the visual thalamus, including the A lamina of the dorsal lateral geniculate nucleus (LGN), the medial interlaminar nucleus (MIN), the lateral posterior nucleus (LP), and the pulvinar nucleus (PUL). To identify TRN terminals, we injected biocytin into the visual sector of the TRN to label terminals by anterograde transport. We then used postembedding immunocytochemical staining for GABA to distinguish TRN terminals as biocytin-labeled GABA-positive terminals and to distinguish the postsynaptic targets of TRN terminals as GABA-negative thalamocortical cells or GABA-positive interneurons. We found that, in all nuclei, the TRN provides GABAergic input primarily to thalamocortical relay cells (93-100%). Most of this input seems targeted to peripheral dendrites outside of glomeruli. The TRN does not appear to be a significant source of GABAergic input to interneurons in the visual thalamus. We also examined the synaptic targets of the overall population of GABAergic axon terminals (F1 profiles) within these same regions of the visual thalamus and found that the TRN contacts cannot account for all F1 profiles. In addition to F1 contacts on the dendrites of thalamocortical cells, which presumably include TRN terminals, another population of F1 profiles, most likely interneuron axons, provides input to GABAergic interneuron dendrites. Our results suggest that the TRN terminals are ideally situated to modulate thalamocortical transmission by controlling the response mode of thalamocortical cells.


Subject(s)
Cats/anatomy & histology , Synapses/ultrastructure , Thalamic Nuclei/cytology , Visual Pathways/cytology , Animals , Geniculate Bodies/cytology , Interneurons/chemistry , Interneurons/ultrastructure , Intralaminar Thalamic Nuclei/cytology , Lateral Thalamic Nuclei/cytology , Microscopy, Electron , Pulvinar/cytology , Synapses/chemistry , gamma-Aminobutyric Acid/analysis
3.
J Virol ; 75(4): 1761-9, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11160674

ABSTRACT

Penciclovir (PCV), an antiherpesvirus agent in the same class as acyclovir (ACV), is phosphorylated in herpes simplex virus (HSV)-infected cells by the viral thymidine kinase (TK). Resistance to ACV has been mapped to mutations within either the TK or the DNA polymerase gene. An identical activation pathway, the similarity in mode of action, and the invariant cross-resistance of TK-negative mutants argue that the mechanisms of resistance to PCV and ACV are likely to be analogous. A total of 48 HSV type 1 (HSV-1) and HSV-2 isolates were selected after passage in the presence of increasing concentrations of PCV or ACV in MRC-5 cells. Phenotypic analysis suggested these isolates were deficient in TK activity. Moreover, sequencing of the TK genes from ACV-selected mutants identified two homopolymeric G-C nucleotide stretches as putative hot spots, thereby confirming previous reports examining Acv(r) clinical isolates. Surprisingly, mutations identified in PCV-selected mutants were generally not in these regions but distributed throughout the TK gene and at similar frequencies of occurrence within A-T or G-C nucleotides, regardless of virus type. Furthermore, HSV-1 isolates selected in the presence of ACV commonly included frameshift mutations, while PCV-selected HSV-1 mutants contained mostly nonconservative amino acid changes. Data from this panel of laboratory isolates show that Pcv(r) mutants share cross-resistance and only limited sequence similarity with HSV mutants identified following ACV selection. Subtle differences between PCV and ACV in the interaction with viral TK or polymerase may account for the different spectra of genotypes observed for the two sets of mutants.


Subject(s)
Acyclovir/analogs & derivatives , Acyclovir/pharmacology , Antiviral Agents/pharmacology , Herpesvirus 1, Human/drug effects , Herpesvirus 2, Human/drug effects , Animals , Autoradiography , Cell Line , DNA, Viral/genetics , Drug Resistance, Microbial , Guanine , Herpesvirus 1, Human/genetics , Herpesvirus 1, Human/physiology , Herpesvirus 2, Human/genetics , Herpesvirus 2, Human/physiology , Humans , Mutation , Sequence Analysis, DNA , Thymidine Kinase/genetics , Thymidine Kinase/metabolism , Viral Plaque Assay
4.
Am J Physiol Renal Physiol ; 279(3): F426-39, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10966922

ABSTRACT

To gain further insights into the molecular mechanisms involved in acute renal failure, we have isolated a new gene from rat and human, named KSP32 (kidney-specific protein with a molecular mass of 32 kDa). KSP32 encodes a novel gene that shows little homology to other mammalian proteins. It, however, shares extensive homology with several proteins found in the nematode Caenorhabditis elegans and plants. The expression of KSP32 mRNA is highly restricted to kidney. In situ hybidization analysis revealed that the expression of KSP32 mRNA was prominent in the boundary of kidney cortex and outer medulla, exhibiting a raylike formation extending from the medulla into the cortex. Finally, KSP32 mRNA was dramatically downregulated in rat following induction of acute ischemic renal failure. Rapid loss of KSP32 mRNA expression was observed beginning at approximately 5 h following renal injury and mRNA levels remained depressed for at least 96 h. Both KSP32 mRNA levels as well as renal function recovered 14 days after injury. Administration of an endothelin receptor antagonist (SB-209670), known to restore renal function, significantly increased KSP32 expression.


Subject(s)
Acute Kidney Injury/physiopathology , Ischemia/physiopathology , Kidney Tubules, Proximal/physiology , Oxidoreductases , Proteins/genetics , Proteins/metabolism , Acute Kidney Injury/metabolism , Animals , Base Sequence , Cloning, Molecular , Down-Regulation/physiology , Gene Expression/physiology , Humans , In Situ Hybridization , Inositol Oxygenase , Ischemia/metabolism , Kidney Medulla/chemistry , Kidney Medulla/physiology , Kidney Tubules, Proximal/blood supply , Kidney Tubules, Proximal/chemistry , Molecular Sequence Data , Oxygenases , Polymerase Chain Reaction , RNA, Messenger/analysis , Rats , Rats, Sprague-Dawley , Sequence Homology, Amino Acid
5.
J Comp Neurol ; 416(4): 509-20, 2000 Jan 24.
Article in English | MEDLINE | ID: mdl-10660881

ABSTRACT

Previous electron microscopic studies of synaptic terminal distributions in the lateral geniculate nucleus have been flawed by potential sampling biases favoring larger synapses. We have thus re-investigated this in the geniculate A-laminae of the cat with an algorithm to correct this sampling bias. We used serial reconstructions with the electron microscope to determine the size of each terminal and synaptic type. We observed that RL (retinal) terminals are largest, F (local, GABAergic, inhibitory) terminals are intermediate in size, and RS (cortical and brainstem) terminals are smallest. We also found that synapses from RL terminals are largest, and thus most oversampled, and we used synaptic size data to correct for sampling errors. Doing so, we found that the relative synaptic percentages overall are 11.7% for RL terminals, 27.5% for F, and 60.8% for RS. Furthermore, we distinguished between relay cells and interneurons with post-embedding immunocytochemistry for GABA (relay cells are GABA negative and interneurons are GABA positive). Onto relay cells, RL terminals contributed 7.1%, F terminals contributed 30.9%, and RS terminals contributed 62.0%. Onto interneurons, RL terminals contributed 48.7%, F terminals contributed 24.4%, and RS terminals contributed 26.9%. We also found that RL terminals included many more separate synaptic contact zones (9.1 +/- 1.6) than did F terminals (2.6 +/- 0.2) or RS terminals (1.02 +/- 0.02). We used these data plus the calculation of overall percentages of each synaptic type to compute the relative percentage of each terminal type in the neuropil: RL terminals represent 1.8%, F terminals represent 14.5%, and RS terminals represent 83.7%. We argue that this relative synaptic paucity is typical for driver inputs (from retina), whereas modulator inputs (all others) require many more synapses to achieve their function.


Subject(s)
Cats/anatomy & histology , Geniculate Bodies/ultrastructure , Synapses/ultrastructure , Algorithms , Animals , Geniculate Bodies/metabolism , Image Processing, Computer-Assisted , Immunohistochemistry , Microscopy, Electron , Nerve Endings/metabolism , Nerve Endings/ultrastructure , gamma-Aminobutyric Acid/metabolism
6.
Am J Ophthalmol ; 128(1): 21-30, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10482090

ABSTRACT

PURPOSE: To describe intentional placement of intraocular lens haptics in the ciliary sulcus of patients with uveitis who are at high risk for postoperative posterior synechiae and lens dislocation. METHODS: We reviewed our experience with 16 eyes of 12 patients with uveitis who underwent cataract surgery with ciliary sulcus fixation of intraocular lenses. Patients were followed for a median of 16.5 months (range, 9 to 44 months) after surgery. We evaluated eyes for surgical technique and the following preoperative and postoperative factors: best-corrected visual acuity, intraocular pressure, anterior chamber cells, and posterior synechiae. The following additional postoperative factors were sought: lens dislocation, lens edge capture, and evidence of pigment dispersion. RESULTS: Posterior synechiae were present in 13 eyes before surgery; postoperative posterior synechiae developed in only three of these eyes. These adhesions resulted in lens edge capture in one eye and limited lens decentration in another. Scant pigment was present on the lens optic or in the anterior chamber, suggesting pigment dispersion, in four eyes. We found no evidence of consistently increased anterior segment inflammation or intraocular pressure after surgery when compared with preoperative levels for this group of patients. Postoperative posterior synechiae were seen more often in eyes that had can-opener anterior capsulotomy than in eyes that had continuous, curvilinear capsulorhexis (P = .036). CONCLUSIONS: Ciliary sulcus fixation allows the intraocular lens to serve as a physical barrier between the iris and the lens capsule remnants. This technique may be useful for reducing the risk of postoperative posterior synechiae in patients with uveitis without increasing the risk of other postoperative problems.


Subject(s)
Capsulorhexis , Ciliary Body/surgery , Lens Implantation, Intraocular/methods , Lenses, Intraocular , Phacoemulsification , Suture Techniques , Uveitis, Anterior/complications , Adult , Aged , Aged, 80 and over , Female , Follow-Up Studies , Humans , Intraocular Pressure , Iris Diseases/complications , Male , Middle Aged , Postoperative Complications/prevention & control , Tissue Adhesions , Uveitis, Anterior/pathology , Visual Acuity
7.
Article in English | MEDLINE | ID: mdl-10477044

ABSTRACT

Leukotriene B4 (LTB4) and 12-(R)-hydroxy-5,8,10,14-eicosatetraenoic acid (12-[R]-HETE) have been postulated to contribute to the pathophysiology of inflammatory diseases. SB 201993, (E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4-methoxyphenyl)octyl] oxy]-2-pyridinyl] methyl] thio] methyl] benzoic acid, identified from a chemical series designed as ring-fused analogs of LTB4, was evaluated as an antagonist of LTB4- and 12-(R)-HETE-induced responses in vitro and for anti-inflammatory activity in vivo. SB 201993 competitively antagonized [3-H]-LTB4 binding to intact human neutrophils (Ki = 7.6 nM) and to membranes of RBL 2H3 cells expressing the LTB4 receptor (RBL 2H3-LTB4R; IC50 = 154 nM). This compound demonstrated competitive antagonism of LTB4- and 12-(R)-HETE-induced Ca2+ mobilization responses in human neutrophils (IC50s of 131 nM and 105 nM, respectively) and inhibited LTB4-induced Ca2+ mobilization in human cultured keratinocytes (IC50 = 61 nM), RBL 2H3-LTB4R cells (IC50 = 255 nM) and mouse neutrophils (IC50 = 410 nM). SB 201993 showed weak LTD4-receptor binding affinity (Ki = 1.9 microM) and inhibited 5-lipoxygenase (IC50 of 3.6 microM), both in vitro and ex vivo. In vivo, SB 201993 inhibited LTB4-induced neutrophil infiltration in mouse skin and produced dose-related, long lasting topical anti-inflammatory activity against the fluid and cellular phases of arachidonic acid-induced mouse ear inflammation (ED50 of 580 microg/ear and 390 microg/ear, respectively). Similarly, anti-inflammatory activity was also observed in the murine phorbol ester-induced cutaneous inflammation model (ED50 of 770 and 730 microg/ear, respectively, against the fluid and cellular phases). These results indicate that SB 201993 blocks the actions of LTB4 and 12-(R)-HETE and inhibits a variety of inflammatory responses; and thus may be a useful compound to evaluate the role of these mediators in disease models.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Benzoates/pharmacology , Pyridines/pharmacology , Receptors, Leukotriene B4/antagonists & inhibitors , 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid/pharmacology , Animals , Binding, Competitive , Calcimycin/pharmacology , Calcium/blood , Calcium/metabolism , Cell Membrane/metabolism , Cells, Cultured , Guinea Pigs , Humans , Ionophores/pharmacology , Keratinocytes/drug effects , Keratinocytes/metabolism , Leukotriene B4/blood , Leukotriene B4/pharmacology , Male , Mice , Neutrophils/drug effects , Neutrophils/metabolism
8.
J Comp Neurol ; 390(2): 247-55, 1998 Jan 12.
Article in English | MEDLINE | ID: mdl-9453668

ABSTRACT

Laminae A and A1 of the lateral geniculate nucleus in the cat are generally considered to be a structurally and functionally matched pair of inputs from two eyes, although there are subtle light microscopic and physiological differences. The present study aims to display ultrastructural differences between these two laminae based on electron microscopic observances on the connectivity patterns of their afferents onto two main cell types: relay cells, and interneurons present in this nucleus. In a design of population measurement from randomized sample areas in laminae A and A1 from six brains, all synaptic contacts made by three terminal types of the geniculate nucleus were identified, and a number of relative distribution properties were analyzed. When the A-laminae were considered as a homogeneous structure, the distribution of the three terminal types on geniculate cells was similar to previously reported results, confirming the validity of the sampling strategies used; RLP (retinal) terminals provided one-fifth of all synapses, whereas RD (from cortex and brainstem) and F (inhibitory) types constituted one-half and one-third, respectively. The relay cells alone received a similar composition of afferents. However, interneurons alone received approximately equal amounts of synapses from the three sources. Similar analyses comparing the distributions in lamina A and A1 revealed that RD and F terminals, but not RLP terminals, innervate these two laminae differently; more RD and fewer F terminals were found in lamina A1. This difference was also present in the distribution of terminals on relay cells alone, but not on interneurons. These results suggest that (1) retinal terminals form a significantly larger fraction of the input to interneurons than to relay cells; correspondingly, cortex and brainstem provide a smaller fraction of all inputs to interneurons than to relay cells; and (2) laminae A and A1 are not strictly equivalent projection sites of the two retinae. The results are discussed in relation to the Y-cell subpopulation in lamina A1 that is involved in corticotectal, as well as corticogeniculate circuits, as opposed to Y-cells of lamina A that are involved in only the latter.


Subject(s)
Brain Mapping , Cats/physiology , Geniculate Bodies/ultrastructure , Interneurons/physiology , Synapses/physiology , Animals , Microscopy, Electron
9.
Am J Respir Cell Mol Biol ; 17(1): 106-13, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9224216

ABSTRACT

DNA differential display analysis (DD-PCR) was utilized to identify genes that are expressed in airway epithelium and are relevant to airway inflammation; cytokine-mediated induction of gene expression and inhibition of that induction by glucocorticoids were the criteria for selection. The IB3-1 cell line was cultured in the presence of tumor necrosis factor-alpha (TNF-alpha), dexamethasone, or dimethyl sulfoxide (DMSO) as a control, and analyzed via DD-PCR and Northern blot analyses. With this approach, two TNF-alpha-inducible and dexamethasone (DEX)-sensitive expressed sequence tags (EST8 and EST19) were identified. In IB3-1 cells, TNF-alpha increased messenger RNA (mRNA) expression of EST8 (34%, P < or = 0.005) and EST19 (41%, P < or = 0.01), whereas dexamethasone reduced this expression to resting levels. This pattern of mRNA expression was also observed in normal human bronchial epithelial cells (EST8: 21%, P < or = 0.009; EST19: 11%, P < or = 0.02) and in the basophil leukemia cell line KU812 (EST8: 34%, P < or = 0.01). Through basic local alignment search tool (BLAST) analysis, it was determined that these ESTs exhibited significant homology with the monomeric G protein rhoC (EST8: 100% homology, P = 1.6 x 10(-100)) and the UFO tyrosine kinase receptor (EST19: 86% homology, 5.3 x 10(-28).


Subject(s)
Bronchi/metabolism , DNA , Gene Expression , Polymerase Chain Reaction/methods , Transcription, Genetic , Base Sequence , Cell Line , Cloning, Molecular , Cytokines/pharmacology , Data Display , Dexamethasone/pharmacology , Dimethyl Sulfoxide/pharmacology , Epithelium/metabolism , Gene Expression/drug effects , Glucocorticoids/pharmacology , Humans , Inflammation , Molecular Sequence Data , RNA, Messenger/biosynthesis , Sequence Alignment , Sequence Homology, Nucleic Acid , Sequence Tagged Sites , Transcription, Genetic/drug effects , Tumor Cells, Cultured , Tumor Necrosis Factor-alpha/pharmacology
10.
Genomics ; 41(2): 169-76, 1997 Apr 15.
Article in English | MEDLINE | ID: mdl-9143491

ABSTRACT

Human cathepsin K is a recently described cysteine protease with high sequence homology to cathepsins S and L, members of the papain superfamily of cysteine proteases. Cathepsin K is abundantly and selectively expressed in osteoclasts and may perform a specialized role in osteoclast-mediated bone resorption. In the present study, the genomic organization and chromosomal localization of human cathepsin K (HGMW-approved symbol CTSK) were determined. Intron-exon boundaries were identified by PCR on human genomic DNA, and subsequently a P1 genomic clone containing the full-length gene was isolated. Cathepsin K spans approximately 12.1 kb of genomic DNA and is composed of eight exons and seven introns. The genomic organization of cathepsin K is similar to that of cathepsins S and L. The gene was mapped to chromosome 1q21 by fluorescence in situ hybridization. Primer walking on the P1 genomic clone identified 1108 bp of 5' flanking sequence and 459 bp of 3' flanking sequence. Ribonuclease protection assay and 5' RACE indicated a single transcriptional start site 49 bp upstream of the initiator Met codon. Analysis of the 5' flanking region indicates that this gene lacks canonical TATA and CAAT boxes and contains multiple potential transcription regulatory sites. The characterization of the cathepsin K gene and its promoter may provide valuable insights not only into its osteoclast-selective expression, but also into the molecular mechanisms responsible for osteoclast activation.


Subject(s)
Cathepsins/genetics , Chromosomes, Human, Pair 1 , Base Sequence , Binding Sites , Cathepsin K , Chromosome Mapping , DNA, Complementary , Genome , Humans , In Situ Hybridization, Fluorescence , Molecular Sequence Data , Transcription, Genetic
11.
Proc Natl Acad Sci U S A ; 94(4): 1517-20, 1997 Feb 18.
Article in English | MEDLINE | ID: mdl-9037085

ABSTRACT

Terminals of a morphological type known as RD (for round vesicles and dense mitochondria, which we define here as the aggregate of types formerly known as RSD and RLD, where "S" is small and "L" is large) constitute at least half of the synaptic inputs to the feline lateral geniculate nucleus, which represents the thalamic relay of retinal input to cortex. It had been thought that the vast majority of these RD terminals were of cortical origin, making the corticogeniculate pathway by far the largest source of input to geniculate relay cells. However, another source of RD terminals recently identified derives from cholinergic cells of the brainstem parabrachial region. (These cells also contain NO.) We used techniques of electron microscopy to determine quantitatively the relative contribution of cortex and brainstem to the population of RD terminals. We identified corticogeniculate terminals by orthograde transport of biocytin injected into the visual cortex and identified brainstem terminals by immunocytochemical labeling for choline acetyltransferase or brain NO synthase (the synthesizing enzymes for acetylcholine and NO, respectively). We estimated the relative numbers of corticogeniculate and brainstem terminals with a two-step algorithm: First, we determined the relative probability of sampling each terminal type in our material, and then we calculated what mixture of identified corticogeniculate and brainstem terminals was needed to recreate the size distribution of the parent RD terminal population. We conclude that brainstem terminals comprise roughly one-half of the RD population. Thus, the cortical input is perhaps half as large and the brainstem input is an order of magnitude larger than had been thought. This further suggests that the brainstem inputs might play a surprisingly complex and subtle role in the control of the geniculocortical relay.


Subject(s)
Brain Stem , Geniculate Bodies/ultrastructure , Neural Pathways , Synapses/ultrastructure , Visual Cortex , Algorithms , Animals , Axonal Transport , Cats , Choline O-Acetyltransferase/isolation & purification , Immunohistochemistry , Lysine/analogs & derivatives , Lysine/metabolism
12.
J Comp Neurol ; 377(4): 535-49, 1997 Jan 27.
Article in English | MEDLINE | ID: mdl-9007191

ABSTRACT

We used immunohistochemistry in cats to demonstrate the presence of brain nitric oxide synthase (BNOS) in cholinergic fibers within the A-laminae of the lateral geniculate nucleus. We used a double labeling procedure with electron microscopy and found that all terminals labeled for choline acetyltransferase (ChAT) in the geniculate A-laminae were double labeled for BNOS. Also, some interneuron dendrites, identified by labeling for gamma-aminobutyric acid (GABA), contained BNOS, but relay cell dendrites did not. We then compared parabrachial and corticogeniculate terminals, identifying the former by BNOS/ChAT labeling and the latter by orthograde transport of biocytin injected into cortical area 17, 18, or 19. All corticogeniculate terminals and most BNOS- or ChAT-positive brainstem terminals displayed RSD morphology, whereas some brainstem terminals exhibited RLD morphology. However, parabrachial terminals were larger, on average, than corticogeniculate terminals. We also found that parabrachial terminals were located both inside and outside of glomeruli, and they always contacted relay cell dendrites proximally among retinal terminals (the retinal recipient zone). In contrast, the cortical terminals were limited to peripheral dendrites (the cortical recipient zone). Thus, little if any overlap exists in the distribution of parabrachial and corticogeniculate terminals on the dendrites of relay cells.


Subject(s)
Brain Mapping , Cats/physiology , Geniculate Bodies/enzymology , Mesencephalon/physiology , Nerve Endings/enzymology , Visual Cortex/physiology , Animals , Cats/metabolism , Immunohistochemistry , Nitric Oxide Synthase/analysis , Visual Pathways/enzymology
13.
J Neurosci ; 16(24): 8181-92, 1996 Dec 15.
Article in English | MEDLINE | ID: mdl-8987843

ABSTRACT

Glutamate has an important neuromodulatory role in synaptic transmission through metabotropic glutamate receptors (mGluRs) linked to a variety of G-protein-coupled second messenger pathways. Activation of these receptors on relay cells in the lateral geniculate nucleus (LGN) with the agonist trans-(1S,3R)-1-amino-1, 3-cyclopentanedicarboxylic acid produces a membrane depolarization that inactivates the low-threshold Ca2+ spike, causing a transition from burst to tonic response mode. The excitatory effects of metabotropic receptor activation in the LGN appear to be produced through the receptors linked to phosphoinositide hydrolysis and apparently only through activation of the corticogeniculate pathway. Two mGluRs, mGluR1alpha (a splice variant of mGluR1) and mGluR5, are linked to the phosphoinositide system. We examined the localization of these receptors with affinity-purified, anti-peptide, polyclonal antibodies raised to the C-terminal region of each receptor protein. Under examination with the light microscope, we found that both types of receptors are present in the geniculate neuropil and in that of the overlying thalamic reticular nucleus, including the perigeniculate nucleus. We also examined the ultrastructural localization of immunolabel with the electron microscope, using a postembedding immunogold marker to identify terminals, dendrites, and somata that contain GABA. Label for the antibody directed against mGluR1alpha was primarily localized in the dendrites of relay cells, postsynaptic to various terminal types. Of these, terminal profiles normally associated with corticogeniculate inputs predominated, whereas retinal terminal profiles were scarce. Label for the antibody directed against mGluR5 label was prominent in inhibitory F2-terminal profiles associated with the retinal input to relay cells. In the perigeniculate nucleus, both mGluRs were localized to dendrites. The distribution of the two phosphoinositide-linked mGluRs in the LGN suggests very different functional roles for the two receptor types. We conclude from these data that mGluR1 appears to have a dominant role in corticogeniculate control of response mode through the feedback glutamatergic pathway from layer VI, whereas mGluR5 is positioned to affect retinogeniculate activation of relay cells through feed forward glomerular interactions.


Subject(s)
Cerebral Cortex/physiology , Geniculate Bodies/physiology , Receptors, Metabotropic Glutamate/physiology , Retina/physiology , Afferent Pathways/physiology , Animals , Cats , Dendrites/metabolism , Dendrites/ultrastructure , Geniculate Bodies/metabolism , Geniculate Bodies/ultrastructure , Immunohistochemistry , Microscopy, Electron , Nerve Endings/physiology , Nerve Endings/ultrastructure , Receptors, Metabotropic Glutamate/metabolism , Synapses/physiology , Synapses/ultrastructure , Tissue Distribution
14.
Am J Ophthalmol ; 122(4): 520-5, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8862049

ABSTRACT

PURPOSE: To compare measurements of optic nerve topography of ocular hypertensive patients with those of normal subjects and primary open-angle glaucoma patients. METHODS: Three age-matched study groups of 46 ocular hypertensive patients, 46 primary open-angle glaucoma patients, and 46 normal subjects were recruited from patients and volunteers of a glaucoma referral practice. Optic nerve topography was measured using a confocal scanning laser tomograph, the Heidelberg Retina Tomograph. The following optic nerve parameters were evaluated: disk area, cup/disk area ratio, cup shape, height in contour, rim area, rim volume, maximum cup depth, cup area, cup volume, retinal height, and retinal cross-section area. For this cross-sectional study, analysis of variance was used to evaluate overall differences among the three subject groups and the Tukey-Kramer multiple comparison test to evaluate differences between the means of two groups. RESULTS: Statistically significant differences among study groups were found for all topographic optic nerve parameters evaluated. Despite considerable overlap in optic nerve parameter measurements among the study groups, mean values of ocular hypertensive eyes were intermediate between those for normal and primary open-angle glaucoma eyes. Statistically significant differences were found between ocular hypertensive and glaucomatous eyes for all optic nerve parameters measured, and between ocular hypertensive and normal eyes for disk area, height in contour, rim area, and rim volume. CONCLUSIONS: In age-matched groups, mean measurements of certain topographic optic nerve parameters of ocular hypertensive eyes differ from those of normal and glaucomatous eyes.


Subject(s)
Glaucoma, Open-Angle/pathology , Lasers , Ocular Hypertension/pathology , Ophthalmoscopy/methods , Optic Disk/pathology , Optic Nerve/pathology , Cross-Sectional Studies , Humans , Middle Aged , Tomography/instrumentation
15.
Genome Res ; 6(10): 980-5, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8908517

ABSTRACT

Defects in the human GALK1 gene result in galactokinase deficiency and cataract formation. We have isolated this gene and established its structural organization. The gene contains 8 exons and spans approximately 7.3 kb of genomic DNA. The GALK1 promoter was localized and found to have many features in common with other housekeeping genes, including high GC content, several copies of the binding site for the Sp1 transcription factor, and the absence of TATA-box and CCAAT-box motifs typically present in eukaryotic Pol II promoters. Analysis by 5'-RACE PCR indicates that the GALK1 mRNA is heterogeneous at the 5' terminus, with transcription sites occurring at many locations between 21 and 61 bp upstream of the ATG start site of the coding region. In vitro translation experiments of the GALK1 cDNA indicate that the protein is cytosolic and not associated with the endoplasmic reticulum membrane.


Subject(s)
Galactokinase/genetics , Amino Acid Sequence , Base Sequence , DNA, Complementary , Exons , Humans , Introns , Molecular Sequence Data , Promoter Regions, Genetic , Transcription, Genetic
16.
J Biol Chem ; 271(14): 8488-92, 1996 Apr 05.
Article in English | MEDLINE | ID: mdl-8626550

ABSTRACT

CSBP p38 is a mitogen-activated protein kinase that is activated in response to stress, endotoxin, interleukin 1, and tumor necrosis factor. Using a catalytically inactive mutant (D168A) of human CSBP2 as the bait in a yeast two-hybrid screen, we have identified and cloned a novel kinase which shares approximately 70% amino acid identity to mitogen-activated protein kinase-activated protein kinase (MAPKAP kinase)-2, and thus was designated MAPKAP kinase-3. The binding of CSBP to MAPKAP kinase-3 was confirmed in vitro by the precipitation of epitope-tagged CSBP1, CSBP2, and CSBP2(D168A) and endogenous CSBP from mammalian cells by a bacterially expressed GST-MAPKAP kinase-3 fusion protein and in vivo by co-precipitation of the epitope-tagged proteins co-expressed in HeLa cells. MAPKAP kinase-3 was phosphorylated by both CSBP1 and CSBP2 and was then able to phosphorylate HSP27 in vitro. Treatment of HeLa cells with sorbitol or TNF resulted in activation of CSBP and MAPKAP kinase-3 and activation of MAPKAP kinase-3 could be blocked by preincubation of cells with SB203580, a specific inhibitor of CSBP kinase activity. These data suggest that MAPKAP kinase-3 is activated by stress and cytokines and is a novel substrate of CSBP both in vitro and in vivo.


Subject(s)
Calcium-Calmodulin-Dependent Protein Kinases/metabolism , Mitogen-Activated Protein Kinases , Protein Serine-Threonine Kinases/genetics , Amino Acid Sequence , Animals , Cells, Cultured , Chlorocebus aethiops , Cloning, Molecular , HeLa Cells , Heat-Shock Proteins/metabolism , Humans , Intracellular Signaling Peptides and Proteins , Molecular Sequence Data , Protein Binding , Protein Serine-Threonine Kinases/metabolism , Sequence Alignment , Sequence Homology, Amino Acid , Substrate Specificity , p38 Mitogen-Activated Protein Kinases
17.
Am J Ophthalmol ; 120(6): 732-8, 1995 Dec.
Article in English | MEDLINE | ID: mdl-8540546

ABSTRACT

PURPOSE: To evaluate the association between quantitative nerve fiber layer measurements and visual field loss in patients with primary open-angle glaucoma. METHODS: Quantitative retinal nerve fiber layer measurements were obtained in 53 patients with primary open-angle glaucoma by using confocal scanning laser ophthalmoscopy (cross-section area) and confocal scanning laser polarimetry (retardation ratio). For each eye, three images were obtained with each instrument. An image that was the mean of those three was created and used in all analyses. We investigated the association between global, regional, and hemifield differences in retinal nerve fiber layer measurements and visual field loss with linear regression techniques. RESULTS: The retardation ratio decreased with increasing mean visual field loss, measured both globally and regionally; R2 (the amount of variation explained by the model) ranged from 8% to 21%. Retinal nerve fiber layer cross-section area was not significantly associated with global measures of visual field loss. The inferior visual field mean deviation increased with decreasing superior retinal nerve fiber layer cross-section area (R2 = 8.2%, P = .04); superior visual field mean deviation was not associated with inferior retinal nerve fiber layer cross-section area (R2 = 2.6%, P = .25). Hemifield differences in visual field mean deviation increased with increasing hemifield differences in retinal nerve fiber layer cross-section area (R2 = 20.0%, P < .001), but not with retardation ratio (R2 = 0.9%, P = .48). CONCLUSIONS: Quantitative measures of the retinal nerve fiber layer using both confocal scanning laser ophthalmoscopy and confocal scanning laser polarimetry were correlated with visual field loss in glaucoma patients.


Subject(s)
Glaucoma/pathology , Glaucoma/physiopathology , Retina/pathology , Visual Fields , Aged , Female , Humans , Male , Microscopy, Confocal , Middle Aged , Nerve Fibers/pathology
18.
Biochem Biophys Res Commun ; 209(2): 385-92, 1995 Apr 17.
Article in English | MEDLINE | ID: mdl-7733904

ABSTRACT

A full-length clone encoding the human VIP-2 receptor was isolated from a human placenta cDNA library. The 1317-bp cDNA insert encodes a protein of 438 amino acids which is a member of the seven transmembrane domain G-protein-coupled receptor superfamily. Expression of the human VIP-2 receptor in COS-7 cells confered high affinity binding to [125I] VIP (IC50 = 0.93 nM), which was displaced by unlabeled PACAP-38 (IC50 = 6.2 nM). VIP and PACAP-38 were equipotent in stimulating accumulation of cAMP in COS-7 cells transfected with the human VIP-2 receptor. Northern blot analysis revealed two VIP-2 receptor mRNAs of 4.6 kb and 2.3 kb in size which were expressed predominantly in the human skeletal muscle and to a lesser extent in the human brain, heart, pancreas and placenta.


Subject(s)
Receptors, Vasoactive Intestinal Peptide/genetics , Amino Acid Sequence , Animals , Base Sequence , Cloning, Molecular , Gene Expression , Humans , Molecular Sequence Data , Oligonucleotide Probes/chemistry , RNA, Messenger/genetics , Rats , Receptors, Vasoactive Intestinal Peptide, Type II , Sequence Alignment , Sequence Homology, Amino Acid
19.
J Comp Neurol ; 348(4): 481-510, 1994 Oct 22.
Article in English | MEDLINE | ID: mdl-7836559

ABSTRACT

We examined the projection from the basal forebrain to thalamic and cortical regions of the visual system in cats, with particular reference to the visual sector of the thalamic reticular nucleus, the lateral geniculate nucleus, and the striate cortex. First, we made injections of wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP) into the visual sector of the thalamic reticular nucleus and found cells labeled by retrograde transport in the lateral nucleus basalis magnocellularis. Injection of biocytin into the basal forebrain resulted in the anterograde labeling of a dense band of fibers and terminals within the entire thalamic reticular nucleus; this labeling extended through the visual sector including the perigeniculate nucleus. No orthograde labeling was found in the lateral geniculate nucleus. Next, we addressed the issue of putative neurotransmitters used by this pathway using a variety of immunocytochemical and histochemical markers. In this fashion, we identified two populations of cells in the nucleus basalis magnocellularis of the cat; large cholinergic cells that contain choline acetyltransferase, NADPH-diaphorase, and calbindin and that project to striate cortex and smaller cells that contain gamma-aminobutyric acid (GABA), glutamic acid decarboxylase, and parvalbumin and that project to the visual sector of the thalamic reticular nucleus. We also examined at the electron microscopic level terminals in the visual sector of the thalamic reticular nucleus that were labeled from a biocytin injection in the basal forebrain. Most of these terminals form symmetric contacts onto dendrites and were revealed by postembedding immunocytochemical staining to be positive for GABA.


Subject(s)
Cats/anatomy & histology , Prosencephalon/anatomy & histology , Thalamic Nuclei/anatomy & histology , gamma-Aminobutyric Acid/physiology , Acetylcholine/physiology , Animals , Histocytochemistry , Immunohistochemistry , Neural Pathways/anatomy & histology , Neurons/physiology , Prosencephalon/cytology
20.
J Comp Neurol ; 259(2): 165-92, 1987 May 08.
Article in English | MEDLINE | ID: mdl-3584556

ABSTRACT

In order to describe the circuitry of a single retinal X-cell axon in the lateral geniculate nucleus, we physiologically characterized such an axon in the optic tract and injected it intra-axonally with horseradish peroxidase. Subsequently, we recovered the axon and employed electron microscopic techniques to examine the distribution of synapses from 18% of its labeled terminals by reconstructing the unlabeled postsynaptic neurons through a series of 1,200 consecutive thin sections. We found remarkable selectivity for the axon's output, since only four of the 43 available neurons in a limited portion of the terminal arbor receive synapses from labeled terminals. Moreover, the distribution of these synapses on the four neurons, which we term cells 1 through 4, varies with respect to synapses from other classes of terminals that contact the same cells, including synapses from unlabeled retinal terminals. For cells 1 and 3, the labeled terminals provide 49% and 33%, respectively, of their retinal synapses, and these are located on both dendritic shafts and appendages. Synapses from the injected axon to these cells are thus integrated with those from other retinal axons. For cell 2, the labeled terminals provide 100% of its retinal synapses, but these synapses converge on clusters of dendritic appendages where they are integrated with convergent inhibitory inputs. Finally, for cell 4, the labeled terminals provide less than 2% of its retinal inputs, and these are distally located; we suggest that these synapses are remnants of physiologically inappropriate miswiring that occurs during development. The findings from this study support a concept of selectivity in neuronal circuitry in the mammalian central nervous system and also reveal some of the diverse integrative properties of neurons in the lateral geniculate nucleus.


Subject(s)
Geniculate Bodies/ultrastructure , Retina/ultrastructure , Retinal Ganglion Cells/ultrastructure , Synapses/ultrastructure , Animals , Axons/ultrastructure , Cats , Dendrites/ultrastructure , Horseradish Peroxidase , Microscopy, Electron , Neurons/classification , Neurons/ultrastructure , Visual Pathways/physiology , Visual Pathways/ultrastructure
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