Identification and differential subcellular localization of the neuronal class C and class D L-type calcium channel alpha 1 subunits

To identify and localize the protein products of genes encoding distinct L-type calcium channels in central neurons, anti-peptide antibodies specific for the class C and class D alpha 1 subunits were produced. Anti-CNC1 directed against class C immunoprecipitated 75% of the L-type channels solubilized from rat cerebral cortex and hippocampus. Anti-CND1 directed against class D immunoprecipitated only 20% of the L-type calcium channels. Immunoblotting revealed two size forms of the class C L-type alpha 1 subunit, LC1 and LC2, and two size forms of the class D L-type alpha 1 subunit, LD1 and LD2. The larger isoforms had apparent molecular masses of approximately 200-210 kD while the smaller isoforms were 180-190 kD, as estimated from electrophoresis in gels polymerized from 5% acrylamide. Immunocytochemical studies using CNC1 and CND1 antibodies revealed that the alpha 1 subunits of both L-type calcium channel subtypes are localized mainly in neuronal cell bodies and proximal dendrites. Relatively dense labeling was observed at the base of major dendrites in many neurons. Staining in more distal dendritic regions was faint or undetectable with CND1, while a more significant level of staining of distal dendrites was observed with CNC1, particularly in the dentate gyrus and the CA2 and CA3 areas of the hippocampus. Class C calcium channels were concentrated in clusters, while class D calcium channels were generally distributed in the cell surface membrane of cell bodies and proximal dendrites. Our results demonstrate multiple size forms and differential localization of two subtypes of L-type calcium channels in the cell bodies and proximal dendrites of central neurons. The differential localization and multiple size forms may allow these two channel subtypes to participate in distinct aspects of electrical signal integration and intracellular calcium signaling in neuronal cell bodies. The preferential localization of these calcium channels in cell bodies and proximal dendrites implies their involvement in regulation of calcium-dependent functions occurring in those cellular compartments such as protein phosphorylation, enzyme activity, and gene expression.

[1]  K. Campbell,et al.  The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel , 1988, Trends in Neurosciences.

[2]  H. Chin,et al.  Rat brain expresses an alternatively spliced form of the dihydropyridine-sensitive L-type calcium channel alpha 2 subunit. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[3]  P Hess,et al.  Calcium channels in vertebrate cells. , 1990, Annual review of neuroscience.

[4]  T. Snutch,et al.  Primary structure of a calcium channel that is highly expressed in the rat cerebellum. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[5]  R. J. Miller,et al.  Multiple calcium channels and neuronal function. , 1987, Science.

[6]  K. Campbell,et al.  Solubilization and biochemical characterization of the high affinity [3H]ryanodine receptor from rabbit brain membranes. , 1990, The Journal of biological chemistry.

[7]  T. Murphy,et al.  L-type voltage-sensitive calcium channels mediate synaptic activation of immediate early genes , 1991, Neuron.

[8]  H. Lester,et al.  Rat brain expresses a heterogeneous family of calcium channels. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[9]  M. Greenberg,et al.  The regulation and function of c-fos and other immediate early genes in the nervous system , 1990, Neuron.

[10]  B. Bean,et al.  Classes of calcium channels in vertebrate cells. , 1989, Annual review of physiology.

[11]  S. Narumiya,et al.  Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel , 1989, Nature.

[12]  R. B. Merrifield Solid phase peptide synthesis. I. the synthesis of a tetrapeptide , 1963 .

[13]  A. Brown,et al.  Induction of calcium currents by the expression of the α1-subunit of the dihydropyridine receptor from skeletal muscle , 1989, Nature.

[14]  William A. Catterall,et al.  Clustering of L-type Ca2+ channels at the base of major dendrites in hippocampal pyramidal neurons , 1990, Nature.

[15]  B. Jaffe,et al.  Methods of Hormone Radioimmunoassay , 1974 .

[16]  C. A. Thomas,et al.  Molecular cloning. , 1977, Advances in pathobiology.

[17]  K. Campbell,et al.  Sequence and expression of MRNAs encoding the α1 and α2 subunits of a DHP-sensitive calcium channel , 1988 .

[18]  J. Rosenbluth SUBSURFACE CISTERNS AND THEIR RELATIONSHIP TO THE NEURONAL PLASMA MEMBRANE , 1962, The Journal of cell biology.

[19]  K. Mizuno,et al.  Monoclonal Antibody , 2020, Definitions.

[20]  M. Biel,et al.  Primary structure of the beta subunit of the DHP-sensitive calcium channel from skeletal muscle. , 1989, Science.

[21]  T. Reese,et al.  Similarity of junctions between plasma membranes and endoplasmic reticulum in muscle and neurons , 1976, The Journal of cell biology.

[22]  K. Siegesmund The fine structure of subsurface cisterns , 1968, The Anatomical record.

[23]  P. Lory,et al.  Acceleration of activation and inactivation by the β subunit of the skeletal muscle calcium channel , 1991, Nature.

[24]  P. Ellinor,et al.  Molecular cloning of multiple subtypes of a novel rat brain isoform of the α 1 subunit of the voltage-dependent calcium channel , 1991, Neuron.

[25]  R Llinás,et al.  Blocking and isolation of a calcium channel from neurons in mammals and cephalopods utilizing a toxin fraction (FTX) from funnel-web spider poison. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[26]  S. Vincent,et al.  Structure and functional expression of a member of the low voltage-activated calcium channel family. , 1993, Science.

[27]  W. Catterall,et al.  Subunit structure of dihydropyridine-sensitive calcium channels from skeletal muscle. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[28]  D. Logothetis,et al.  Elementary properties and pharmacological sensitivities of calcium channels in mammalian peripheral neurons , 1989, Neuron.

[29]  M. Smith,et al.  Expression of dihydropyridine‐sensitive brain calcium channels in the rat central nervous system , 1992, FEBS letters.

[30]  M. Adams,et al.  P-type calcium channels blocked by the spider toxin ω-Aga-IVA , 1992, Nature.

[31]  J. Nagy,et al.  [3H]Ryanodine binding sites in rat brain demonstrated by membrane binding and autoradiography , 1991, Brain Research.

[32]  C. Kozak,et al.  A brain L-type calcium channel alpha 1 subunit gene (CCHL1A2) maps to mouse chromosome 14 and human chromosome 3. , 1991, Genomics.

[33]  W. Catterall,et al.  Specific phosphorylation of a COOH-terminal site on the full-length form of the alpha 1 subunit of the skeletal muscle calcium channel by cAMP-dependent protein kinase. , 1992, The Journal of biological chemistry.

[34]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[35]  T. Deerinck,et al.  Identification and localization of ryanodine binding proteins in the avian central nervous system , 1990, Neuron.

[36]  M S Doscher,et al.  Solid-phase peptide synthesis. , 1977, Methods in enzymology.

[37]  S. Fleischer,et al.  Biochemistry and biophysics of excitation-contraction coupling. , 1989, Annual review of biophysics and biophysical chemistry.

[38]  H. Glossmann,et al.  Molecular properties of calcium channels. , 1990, Reviews of physiology, biochemistry and pharmacology.

[39]  T. Snutch,et al.  Distinct calcium channels are generated by alternative splicing and are differentially expressed in the mammalian CNS , 1991, Neuron.

[40]  K. Mikoshiba,et al.  Molecular Diversity of Voltage‐Dependent Calcium Channel , 1993, Annals of the New York Academy of Sciences.

[41]  K. De Jongh,et al.  Subunits of purified calcium channels: a 212-kDa form of alpha 1 and partial amino acid sequence of a phosphorylation site of an independent beta subunit. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[42]  V. Flockerzi,et al.  Primary structure of the receptor for calcium channel blockers from skeletal muscle , 1987, Nature.

[43]  W. Catterall,et al.  Subunit structure and localization of dihydropyridine-sensitive calcium channels in mammalian brain, spinal cord, and retina , 1990, Neuron.

[44]  K. Mikoshiba,et al.  Two types of ryanodine receptors in mouse brain: Skeletal muscle type exclusively in Purkinje cells and cardiac muscle type in various neurons , 1992, Neuron.

[45]  J. Nakai,et al.  Primary structure and functional expression from complementary DNA of a brain calcium channel , 1991, Nature.

[46]  Michael E. Adams,et al.  P-type calcium channels in rat central and peripheral neurons , 1992, Neuron.

[47]  M. Kennedy Regulation of neuronal function by calcium , 1989, Trends in Neurosciences.

[48]  K. De Jongh,et al.  Characterization of the two size forms of the alpha 1 subunit of skeletal muscle L-type calcium channels. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[49]  B. Adams,et al.  Muscular dysgenesis in mice: a model system for studying excitation‐contraction coupling , 1990, The FASEB Journal.

[50]  Y. Mori,et al.  Molecular cloning and characterization of a novel calcium channel from rabbit brain , 1992, FEBS letters.

[51]  A. Fabiato,et al.  Calcium and cardiac excitation-contraction coupling. , 1979, Annual review of physiology.

[52]  Mark E. Williams,et al.  Structure and functional expression of α 1, α 2, and β subunits of a novel human neuronal calcium channel subtype , 1992, Neuron.

[53]  M. Biel,et al.  The roles of the subunits in the function of the calcium channel. , 1991, Science.

[54]  James I. Morgan,et al.  Role of ion flux in the control of c-fos expression , 1986, Nature.