Abstract
Preparations of isolated brain postsynaptic densities (PSDs) contain a characteristic set of proteins among which the most prominent has a molecular weight of approximately 50,000. Following the suggestion that this major PSD protein might be related to a similarly sized component of neurofilaments (F. Blomberg et al., 1977, J. Cell Biol., 74:214- 225), we searched for evidence of neurofilament proteins among the PSD polypeptides. This was done with a novel technique for detecting protein antigens in SDS-polyacrylamide gels (immunoblotting) and an antiserum that was selective for neurofilaments in immunohistochemical tests. As a control, an antiserum against glial filament protein (GFAP) was used because antisera against GFAP stain only glial cells in immunohistochemical tests. They would, therefore, not be expected to react with PSDs that occur only in neurons. The results of these experiments suggested that PSDs contain both neuronal and also glial filament proteins at higher concentrations than either synaptic plasma membranes, myelin, or myelinated axons. However, immunoperoxidase staining of histological sections with the same two antisera gave contradictory results, indicating that PSDs in intact brain tissue contain neither neuronal or glial filament proteins. This suggested that the intermediate filament proteins present in isolated PSD preparations were contaminants. To test this possibility, the proteins of isolated brain intermediate filaments were labeled with 125I and added to brain tissue at the start of a subcellular fractionation schedule. The results of this experiment confirmed that both neuronal and glial filament proteins stick selectively to PSDs during the isolation procedure. The stickiness of PSDs for brain cytoplasmic proteins indicates that biochemical analysis of subcellular fractions is insufficient to establish a given protein as a synaptic junctional component. An immunohistochemical localization of PSDs in intact tissue, which has now been achieved for tubulin, phosphoprotein I, and calmodulin, appears to be an essential accessory item of evidence. Our findings also corroborate recent evidence which suggests that isolated preparations of brain intermediate filaments contain both neuronal and glial filaments.
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- Anderton B. H., Ayers M., Thorpe R. Neurofilaments from mammalian central and peripheral nerve share certain polypeptides. FEBS Lett. 1978 Dec 1;96(1):159–163. doi: 10.1016/0014-5793(78)81083-7. [DOI] [PubMed] [Google Scholar]
- Bhattacharyya B., Volff J. Membrane-bound tubulin in brain and thyroid tissue. J Biol Chem. 1975 Oct 10;250(19):7639–7646. [PubMed] [Google Scholar]
- Blomberg F., Cohen R. S., Siekevitz P. The structure of postsynaptic densities isolated from dog cerebral cortex. II. Characterization and arrangement of some of the major proteins within the structure. J Cell Biol. 1977 Jul;74(1):204–225. doi: 10.1083/jcb.74.1.204. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bloom F. E., Ueda T., Battenberg E., Greengard P. Immunocytochemical localization, in synapses, of protein I, an endogenous substrate for protein kinases in mammalian brain. Proc Natl Acad Sci U S A. 1979 Nov;76(11):5982–5986. doi: 10.1073/pnas.76.11.5982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohen R. S., Blomberg F., Berzins K., Siekevitz P. The structure of postsynaptic densities isolated from dog cerebral cortex. I. Overall morphology and protein composition. J Cell Biol. 1977 Jul;74(1):181–203. doi: 10.1083/jcb.74.1.181. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cotman C. W., Banker G., Churchill L., Taylor D. Isolation of postsynaptic densities from rat brain. J Cell Biol. 1974 Nov;63(2 Pt 1):441–455. doi: 10.1083/jcb.63.2.441. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cotman C. W., Matthews D. A. Synaptic plasma membranes from rat brain synaptosomes: isolation and partial characterization. Biochim Biophys Acta. 1971 Dec 3;249(2):380–394. doi: 10.1016/0005-2736(71)90117-9. [DOI] [PubMed] [Google Scholar]
- Dahl D., Bignami A. Astroglial and axonal proteins in isolated brain filaments. I. Isolation of the glial fibrillary acidic protein and of an immunologically active cyanogen bromide peptide from brain filament preparations of bovine white matter. Biochim Biophys Acta. 1979 Jun 19;578(2):305–316. doi: 10.1016/0005-2795(79)90161-2. [DOI] [PubMed] [Google Scholar]
- Davison P. F., Winslow B. The protein subunit of calf brain neurofilament. J Neurobiol. 1974;5(2):119–133. doi: 10.1002/neu.480050204. [DOI] [PubMed] [Google Scholar]
- De Vries G. H., Eng L. F., Lewis D. L., Hadfield M. G. The protein composition of bovine myelin-free axons. Biochim Biophys Acta. 1976 Jul 19;439(1):133–145. doi: 10.1016/0005-2795(76)90169-0. [DOI] [PubMed] [Google Scholar]
- Feit H., Kelly P., Cotman C. W. Identification of a protein related to tubulin in the postsynaptic density. Proc Natl Acad Sci U S A. 1977 Mar;74(3):1047–1051. doi: 10.1073/pnas.74.3.1047. [DOI] [PMC free article] [PubMed] [Google Scholar]
- GRAY E. G. Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study. J Anat. 1959 Oct;93:420–433. [PMC free article] [PubMed] [Google Scholar]
- GRAY E. G., WHITTAKER V. P. The isolation of nerve endings from brain: an electron-microscopic study of cell fragments derived by homogenization and centrifugation. J Anat. 1962 Jan;96:79–88. [PMC free article] [PubMed] [Google Scholar]
- Gilbert D. S., Newby B. J. Neurofilament disguise, destruction and discipline. Nature. 1975 Aug 14;256(5518):586–589. doi: 10.1038/256586a0. [DOI] [PubMed] [Google Scholar]
- Goldman J. E., Schaumburg H. H., Norton W. T. Isolation and characterization of glial filaments from human brain. J Cell Biol. 1978 Aug;78(2):426–440. doi: 10.1083/jcb.78.2.426. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grab D. J., Berzins K., Cohen R. S., Siekevitz P. Presence of calmodulin in postsynaptic densities isolated from canine cerebral cortex. J Biol Chem. 1979 Sep 10;254(17):8690–8696. [PubMed] [Google Scholar]
- Hoffman P. N., Lasek R. J. The slow component of axonal transport. Identification of major structural polypeptides of the axon and their generality among mammalian neurons. J Cell Biol. 1975 Aug;66(2):351–366. doi: 10.1083/jcb.66.2.351. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones D. H., Matus A. I. Isolation of synaptic plasma membrane from brain by combined flotation-sedimentation density gradient centrifugation. Biochim Biophys Acta. 1974 Aug 9;356(3):276–287. doi: 10.1016/0005-2736(74)90268-5. [DOI] [PubMed] [Google Scholar]
- Kaiserman-Abramof I. R., Peters A. Some aspects of the morphology of Betz cells in the cerebral cortex of the cat. Brain Res. 1972 Aug 25;43(2):527–546. doi: 10.1016/0006-8993(72)90406-4. [DOI] [PubMed] [Google Scholar]
- Kelly P. T., Cotman C. W. Synaptic proteins. Characterization of tubulin and actin and identification of a distinct postsynaptic density polypeptide. J Cell Biol. 1978 Oct;79(1):173–183. doi: 10.1083/jcb.79.1.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Lee V., Yen S. H., Shelanski M. L. Biochemical correlates of astrocytic proliferation in the mutant Staggerer mouse. Brain Res. 1977 Jun 10;128(2):389–392. doi: 10.1016/0006-8993(77)91007-1. [DOI] [PubMed] [Google Scholar]
- Liem R. K., Yen S. H., Salomon G. D., Shelanski M. L. Intermediate filaments in nervous tissues. J Cell Biol. 1978 Dec;79(3):637–645. doi: 10.1083/jcb.79.3.637. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Markwell M. A., Fox C. F. Surface-specific iodination of membrane proteins of viruses and eucaryotic cells using 1,3,4,6-tetrachloro-3alpha,6alpha-diphenylglycoluril. Biochemistry. 1978 Oct 31;17(22):4807–4817. doi: 10.1021/bi00615a031. [DOI] [PubMed] [Google Scholar]
- Matus A. I., NG M., Jones D. H. Immunohistochemical localization of neurofilament antigen in rat cerebellum. J Neurocytol. 1979 Aug;8(4):513–525. doi: 10.1007/BF01214806. [DOI] [PubMed] [Google Scholar]
- Matus A. I., Taff-Jones D. H. Morphology and molecular composition of isolated postsynaptic junctional structures. Proc R Soc Lond B Biol Sci. 1978 Dec 4;203(1151):135–151. doi: 10.1098/rspb.1978.0097. [DOI] [PubMed] [Google Scholar]
- Matus A. I., Walters B. B., Mughal S. Immunohistochemical demonstration of tubulin associated with microtubules and synaptic junctions in mammalian brain. J Neurocytol. 1975 Dec;4(6):733–744. doi: 10.1007/BF01181633. [DOI] [PubMed] [Google Scholar]
- Matus A. I., Walters B. B. Ultrastructure of the synaptic junctional lattice isolated from mammalian brain. J Neurocytol. 1975 Jun;4(3):369–375. doi: 10.1007/BF01102119. [DOI] [PubMed] [Google Scholar]
- PALAY S. L. Synapses in the central nervous system. J Biophys Biochem Cytol. 1956 Jul 25;2(4 Suppl):193–202. doi: 10.1083/jcb.2.4.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PALAY S. L. The morphology of synapses in the central nervous system. Exp Cell Res. 1958;14(Suppl 5):275–293. [PubMed] [Google Scholar]
- Peters A., Kaiserman-Abramof I. R. The small pyramidal neuron of the rat cerebral cortex. The synapses upon dendritic spines. Z Zellforsch Mikrosk Anat. 1969 Sep 22;100(4):487–506. doi: 10.1007/BF00344370. [DOI] [PubMed] [Google Scholar]
- Rueger D. C., Dahl D., Bignami A. Purification of a brain-specific astroglial protein by immunoaffinity chromatography. Anal Biochem. 1978 Sep;89(2):360–371. doi: 10.1016/0003-2697(78)90364-0. [DOI] [PubMed] [Google Scholar]
- Rueger D. C., Huston J. S., Dahl D., Bignami A. Formation of 100 A filaments from purified glial fibrillary acidic protein in vitro. J Mol Biol. 1979 Nov 25;135(1):53–68. doi: 10.1016/0022-2836(79)90340-1. [DOI] [PubMed] [Google Scholar]
- Schachner M., Hedley-Whyte E. T., Hsu D. W., Schoonmaker G., Bignami A. Ultrastructural localization of glial fibrillary acidic protein in mouse cerebellum by immunoperoxidase labeling. J Cell Biol. 1977 Oct;75(1):67–73. doi: 10.1083/jcb.75.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schachner M., Smith C., Schoonmaker G. Immunological distinction between neurofilament and glial fibrillary acidic proteins by mouse antisera and their immunohistological characterization. Dev Neurosci. 1978;1(1):1–14. doi: 10.1159/000112548. [DOI] [PubMed] [Google Scholar]
- Schlaepfer W. W., Hasler M. B. Characterization of the calcium-induced disruption of neurofilaments in rat peripheral nerve. Brain Res. 1979 May 25;168(2):299–309. doi: 10.1016/0006-8993(79)90171-9. [DOI] [PubMed] [Google Scholar]
- Schlaepfer W. W., Lynch R. G. Immunofluorescence studies of neurofilaments in the rat and human peripheral and central nervous system. J Cell Biol. 1977 Jul;74(1):241–250. doi: 10.1083/jcb.74.1.241. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Therien H. M., Mushynski W. E. Isolation of synaptic junctional complexes of high structural integrity from rat brain. J Cell Biol. 1976 Dec;71(3):807–822. doi: 10.1083/jcb.71.3.807. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thorpe R., Delacourte A., Anderton B. H. The isolation of brain 10 nm filament polypeptides from urea-extracts of brain white matter. FEBS Lett. 1979 Jul 1;103(1):148–151. doi: 10.1016/0014-5793(79)81269-7. [DOI] [PubMed] [Google Scholar]
- Thorpe R., Delacourte A., Ayers M., Bullock C., Anderton B. H. The polypeptides of isolated brain 10nm filaments and their association with polymerized tubulin. Biochem J. 1979 Aug 1;181(2):275–284. doi: 10.1042/bj1810275. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tucker R. W., Pardee A. B., Fujiwara K. Centriole ciliation is related to quiescence and DNA synthesis in 3T3 cells. Cell. 1979 Jul;17(3):527–535. doi: 10.1016/0092-8674(79)90261-7. [DOI] [PubMed] [Google Scholar]
- Ueda T., Greengard P., Berzins K., Cohen R. S., Blomberg F., Grab D. J., Siekevitz P. Subcellular distribution in cerebral cortex of two proteins phosphorylated by a cAMP-dependent protein kinase. J Cell Biol. 1979 Nov;83(2 Pt 1):308–319. doi: 10.1083/jcb.83.2.308. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walters B. B., Matus A. I. Tubulin in postynaptic junctional lattice. Nature. 1975 Oct 9;257(5526):496–498. doi: 10.1038/257496a0. [DOI] [PubMed] [Google Scholar]
- Wang Y. J., Mahler H. R. Topography of the synaptosomal membrane. J Cell Biol. 1976 Nov;71(2):639–658. doi: 10.1083/jcb.71.2.639. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yen S. H., Dahl D., Schachner M., Shelanski M. L. Biochemistry of the filaments of brain. Proc Natl Acad Sci U S A. 1976 Feb;73(2):529–533. doi: 10.1073/pnas.73.2.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yen S. H., Liem R. K., Kelly P. T., Cotman C. W., Shelanski M. L. Membrane linked proteins at CNS synapses. Brain Res. 1977 Aug 19;132(1):172–175. doi: 10.1016/0006-8993(77)90717-x. [DOI] [PubMed] [Google Scholar]