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1.
Drug Deliv ; 5(3): 183-95, 1998.
Article in English | MEDLINE | ID: mdl-19569984

ABSTRACT

The objective of this study was to evaluate the potential of P(0) protein, a cell adhesion molecule from peripheral nerve myelin, as a targeting ligand for liposomes. To evaluate binding characteristics and identify possible binding domains, cell-interaction studies were carried out with P(0) protein reconstituted into liposomes (P(0) liposomes) under various conditions. P(0) liposomes with intact P(0) protein were tested after endoglycosidase F treatment (cleaves the carbohydrate moiety) or trypsin digestion (removes the hydrophobic portion, residues 1-79, leaving the carbohydrate portion intact). The cellular uptake was quantitated using radioactive lipids in the liposome bilayer and a liposome-entrapped water soluble compound (inulin). The presence of intact P(0) protein in the liposome bilayer increased the rate of interaction of liposomes 3-4 times with M21 melanoma and HTB-11 neuroblastoma cells (cells of neuroectodermal origin), two times with Caki-1 renal carcinoma cells, and marginally with 3T3 fibroblasts (mesodermal origin). This binding was inhibited by anti-chick P(0) antibodies and Fab fragments. A control transmembrane glycoprotein, glycophorin A., when reconstituted in liposomes had no effect on the binding of liposomes with M21 cells. The results indicate that P(0) protein plays a specific role in the binding of liposomes to cells. Removal of the N-asparagine linked carbohydrate from the P(0) protein in the liposomes resulted in an increase of their association with M21 cells five times that of control liposomes (no protein) and two times that of the non-endoglycosidase F-treated P(0) liposomes. To further characterize the binding domains of P(0) reconstituted into liposomes, competition studies were carried out in the presence of synthetic P(0)-peptides. The competition studies indicated that both the extracellular (residues 90-96) and intracellular (residues 201-207) domain of P(0) protein may be involved in the interaction with cell membranes. The results suggest that P(0) protein is capable of mediating specific heterophilic interactions with various cell lines and targeting to cells of neuroectodermal origin may be achieved.

2.
J Neurosci Res ; 44(6): 594-605, 1996 Jun 15.
Article in English | MEDLINE | ID: mdl-8794951

ABSTRACT

Apolipoprotein A-I (apo A-I), a major apolipoprotein synthesized by liver and intestine to facilitate transport of plasma lipids as lipoproteins, has been detected also in the avian sciatic nerve. The mRNA and protein levels of apo A-I have been shown to increase during the period of rapid myelination (LeBlanc et al.: J Cell Biol 109:1245-1256, 1989). In order to assess the synthesis of apo A-I protein and the processing of apo A-I isoforms during development, endoneurial slices of avian sciatic nerves from chicks during active myelination at 15 and 17 days embryonic and 1 day posthatch age were incubated with [35]S-methionine. The incubations were fractionated into secreted and intracellular fractions, and incorporation of the label was assessed for apo A-I protein. The pattern of labeling of Po protein, as a marker of myelination, was also determined in the intracellular and compact myelin fractions. Methionine incorporation into Po protein was highest in the intracellular compartment at the 15-day embryonic stage and decreased thereafter, with a corresponding increase in the myelin fraction. During these developmental periods, the levels of nascent apo A-I increased in both the secreted and intracellular fractions. The synthesis of apo A-I specifically increases in the secreted fraction compared with total protein synthesis. The processing of the pro-apo A-I is also developmentally regulated. In the intracellular compartment, there are approximately equal proportions of the acidic and basic isoforms. However, with increasing age, a higher proportion of the apo A-I is secreted as acidic isoforms. It is concluded that the secretion and processing of apo A-I is developmentally regulated in the chick sciatic nerve, in parallel with the process of active myelination.


Subject(s)
Apolipoprotein A-I/metabolism , Chickens/metabolism , Sciatic Nerve/metabolism , Animals , Chick Embryo , Electrophoresis, Polyacrylamide Gel , Isoelectric Focusing , Isomerism , Methionine/metabolism , Myelin Sheath/physiology , Nerve Tissue Proteins/biosynthesis , Organ Culture Techniques , Precipitin Tests , Sciatic Nerve/growth & development , Sciatic Nerve/ultrastructure , Subcellular Fractions/metabolism , Sulfur Radioisotopes
3.
Neurochem Res ; 20(10): 1239-48, 1995 Oct.
Article in English | MEDLINE | ID: mdl-8746811

ABSTRACT

Myelin deposition in developing chick sciatic nerve is associated with rapid synthesis of lipids, the major myelin protein Po and apo A-I, a major constituent of plasma lipoproteins. In order to understand possible roles of apo A-I in myelin assembly the synthesis and appearance of Po, apo A-I and lipids was studied in an intracellular fraction, an intralamellar fraction thought to be related to, or derived from, myelin and compact myelin from rapidly myelinating sciatic nerve of 1 day chicks. Incorporation with methionine or pulse-chase experiments indicated that initial synthesis of Po occurs in the intracellular fraction followed by movement to the intralamellar fraction and myelin. Incorporation of labelled oleate into phospholipids suggested that initial synthesis occurs in the intracellular and intralamellar fractions with slow movement to myelin. Incorporation of labelled galactose into cerebrosides suggested that initial synthesis occurs partially in myelin with slow loss from this fraction to the intralamellar fraction. However, incorporation of methionine into apo A-I indicated that initial synthesis occurred in the intracellular fraction with some transfer to the intralamellar fraction and secretion of a major portion into the incubation medium. It is concluded that the subcellular distribution of nascent apo A-I is not well coordinated with the distribution of other nascent constituents of the myelin membrane. The accumulation of nascent Po, phospholipids and cerebrosides in the intralamellar fraction compared to compact myelin suggests that this fraction may play a role as a precursor membrane or as a storage site for assembly of myelin constituents into compact myelin.


Subject(s)
Apolipoprotein A-I/biosynthesis , Cell Compartmentation/physiology , Lipids/biosynthesis , Myelin P0 Protein/biosynthesis , Nerve Fibers, Myelinated/metabolism , Sciatic Nerve/metabolism , Animals , Apolipoprotein A-I/metabolism , Chickens , Lipid Metabolism , Myelin P0 Protein/metabolism , Organ Culture Techniques , Precipitin Tests , Subcellular Fractions/metabolism
4.
Neurochem Res ; 20(3): 269-78, 1995 Mar.
Article in English | MEDLINE | ID: mdl-7541897

ABSTRACT

Apolipoprotein A-I (apo A-I), a soluble lipid transporter, and Po, the major glycoprotein of myelin, are actively synthesized during myelination. To explore the status of post-translational modifications of these proteins in the avian PNS during rapid myelination, endoneurial slices from one day old chick sciatic nerves were incubated with various radioactive precursors that could serve as indicators of such processes. The proteins were isolated from the incubation medium (secreted fraction), the 1% Triton-X-100-soluble intracellular-endoneurial (intracellular) fraction, and myelin-related and purified compact myelin fractions by immunoprecipitation with monospecific anti-apo A-I and or anti-Po antisera. Our results demonstrated that secreted apo A-I is fatty acylated, but not phosphorylated or sulfated. Avian Po protein was phosphorylated by a phorbol ester sensitive protein kinase. Sulfation, as well as fatty acylation, of avian Po protein was observed in organ culture using highly sensitive methods of detection. These results indicate that fatty acylation of secreted apo A-I and phosphorylation, sulfation and fatty acylation of Po have been conserved during evolution, and that these post-translational modifications may play a common function in various species.


Subject(s)
Apolipoprotein A-I/metabolism , Myelin Proteins/metabolism , Protein Processing, Post-Translational , Sciatic Nerve/metabolism , Animals , Chickens , Myelin P0 Protein , Organ Culture Techniques , Rats , Rats, Sprague-Dawley
5.
J Neurosci Res ; 34(1): 14-23, 1993 Jan.
Article in English | MEDLINE | ID: mdl-7678657

ABSTRACT

The effect of a permanent transection on myelin gene expression in a regenerating sciatic nerve and in an adult sciatic nerve was compared to establish the degree of axonal control exerted upon Schwann cells in each population. First, the adult sciatic nerve was crushed, and the distal segment allowed to regenerate. At 12 days post-crush, the sciatic nerve was transected distal to the site of crush to disrupt the Schwann cell-axonal contacts that had reformed. Messenger RNA (mRNA) levels coding for five myelin proteins were assayed in the distal segment of the crush-transected nerve after 9 days and were compared to corresponding levels in the distal segments of sciatic nerves at 21 days post-crush and 21 days post-transection using Northern blot and slot-blot analysis. Levels of mRNAs found in the distal segment of the transected and crush-transected nerve suggested that Schwann cells in the regenerating nerve and in the mature adult nerve are equally responsive to axonal influences. The crush-transected model allowed the genes that were studied to be classified according to their response to Schwann cell-axonal contact. The levels of mRNAs were 1) down-regulated to basal levels (P0 and MBP mRNAs), 2) down-regulated to undetectable levels (myelin-associated glycoprotein mRNAs), 3) upregulated (mRNAs encoding 2'3'-cyclic nucleotide phosphodiesterase and beta-actin), or 4) not stringently controlled by the removal of Schwann cell-axonal contact (proteolipid protein mRNAs). This novel experimental model has thus provided evidence that the expression of some of the important myelin genes during peripheral nerve regeneration is dependent on continuous signals from the ingrowing axons.


Subject(s)
Axons/physiology , Gene Expression Regulation , Myelin Sheath/physiology , Nerve Regeneration/physiology , Sciatic Nerve/physiology , Signal Transduction , Animals , Cell Communication , Denervation , Myelin Basic Protein/genetics , Nerve Crush , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Schwann Cells/physiology , Sciatic Nerve/metabolism
6.
Brain Res Mol Brain Res ; 15(1-2): 40-6, 1992 Sep.
Article in English | MEDLINE | ID: mdl-1279349

ABSTRACT

2',3'-Cyclic nucleotide 3'-phosphodiesterase (CNPase) is an enzyme associated with central nervous system myelination. Although present in the mammalian peripheral nerve, it is not clear what its role is during myelination nor how the expression of this gene is regulated in the PNS. In this study, CNPase gene expression was studied in the crushed and permanently transected rat sciatic nerve, two models of peripheral nerve neuropathy. The Schwann cells of the crushed nerve initially demyelinate, remain in a non-myelinating condition until active regeneration induces remyelination (10-21 days after injury), whereas those of the permanently transected nerve remain in a quiescent, non-myelinating state after the initial demyelination. An increase of CNPase mRNA levels is observed during degeneration and remains high whether the peripheral nerve is regenerating or not, suggesting transcriptional activation of CNPase mRNA and/or increased CNPase mRNA stability as a response to nerve injury. In contrast, the steady state level of CNPase protein did not increase during degeneration or regeneration suggesting either negative translational regulation of CNPase gene expression or a higher turnover of this protein in the injured peripheral nerve. Furthermore, CNPase activity dropped sharply during early degeneration and remained low in the quiescent cells of the permanently transected nerve while it increased in the regenerating nerve. The results suggest that although transcriptional or post-transcriptional regulation of CNPase gene expression is not dependent on Schwann cell-axonal contact, the activity of CNPase appears to be dependent on myelination and indirectly dependent on the presence of axons in the peripheral nerve.


Subject(s)
2',3'-Cyclic-Nucleotide Phosphodiesterases/biosynthesis , Peripheral Nervous System Diseases/enzymology , 2',3'-Cyclic-Nucleotide Phosphodiesterases/metabolism , Animals , Blotting, Northern , Blotting, Western , Gene Expression Regulation, Enzymologic , In Vitro Techniques , Nerve Crush , Nerve Degeneration , RNA/biosynthesis , Rats , Rats, Sprague-Dawley , Sciatic Nerve/metabolism
7.
J Pharm Sci ; 80(11): 1020-8, 1991 Nov.
Article in English | MEDLINE | ID: mdl-1726112

ABSTRACT

The effect of P0 protein (a cell adhesion molecule from avian peripheral nerve myelin) on the rate of interaction of liposomes with human M21 melanoma cells was investigated. Liposome uptake by the cells was quantitated using radioactive lipids and liposome-entrapped drugs under various conditions. Liposomes containing P0 protein and [14C]dipalmitoylphosphatidylcholine:cholesterol (10:1 molar ratio) had an interaction rate with M21 cells three times higher than control vesicles of the same lipid composition but without the protein after incubation at 37 or 4 degrees C. The presence of P0 protein could be detected on the surface of melanoma cells by immunofluorescence after incubation. Binding to the cell surface and endocytosis of P0 liposomes was suggested from the sensitivity of cell-associated proteoliposomes to trypsin, metabolic inhibitors, and low temperature. Liposomal encapsulation highly increased the association of model compounds [( 3H]methotrexate and [3H]inulin) with cells. The proteoliposomes appeared to be leaky in the incubation medium, which led to the delivery of a lower amount of drug into cells than could be expected from their initial drug content. The results suggest that the attachment of liposomes to the cell surface can increase their drug delivery potential, because the binding triggers endocytic processes or a juxtapositional temporary permeability increase of liposome and cellular membrane that can lead to the uptake of drug from liposomes.


Subject(s)
Cell Adhesion Molecules, Neuronal , Melanoma/metabolism , Myelin Proteins , Myelin Sheath/chemistry , Peripheral Nerves/chemistry , Dextrans/administration & dosage , Drug Carriers , Fluorescent Antibody Technique , Folic Acid , Humans , Inulin/administration & dosage , Lipid Metabolism , Liposomes , Methotrexate/administration & dosage , Microscopy, Fluorescence , Myelin P0 Protein , Tumor Cells, Cultured
8.
J Neurochem ; 56(5): 1754-62, 1991 May.
Article in English | MEDLINE | ID: mdl-1707441

ABSTRACT

The proteolipid protein (PLP) is the major protein in the myelin sheath of the CNS. It was recently reported that PLP coding transcripts are also found in the PNS, although the protein was not detectable in peripheral nerve myelin. In the present investigation, levels of mRNA for PLP in sciatic nerve were studied during development and following transection and crush injury. Results were compared to those for P0, the major PNS myelin protein, and the myelin-associated glycoprotein (MAG). PLP transcript levels were very low at 21 days in sciatic nerve and remained unchanged in the adult sciatic nerve. This contrasts markedly with P0 and MAG mRNAs, which are expressed at high levels during development and decrease in content significantly by adulthood. The level of PLP messages was reduced approximately 40% in the quiescent Schwann cells in the distal segment of the sciatic nerve at 21 days after permanent transection, yet P0 mRNA levels were very low, and MAG mRNAs were undetectable in this tissue. The distal segment of the crush-injured sciatic nerve is characterized by transient demyelination followed by rapid myelination. PLP mRNA levels remained comparatively unaffected in the 3-week period following crush injury. RNase protection experiments using two antisense riboprobes confirmed that levels of PLP-derived protected fragments, corresponding to PLP and DM-20 messages, remained unchanged in the developing and adult sciatic nerve. These results indicate that myelin-specific P0 and MAG genes are tightly controlled at the level of transcription through Schwann cell-axonal interactions, whereas PLP transcription in the peripheral nerve remains nearly dissociated from axonal influences.


Subject(s)
Axons/physiology , Proteolipids/genetics , RNA, Messenger/metabolism , Sciatic Nerve/metabolism , Animals , Brain/metabolism , Gene Expression Regulation , Membrane Glycoproteins , Myelin P0 Protein , Myelin Proteins/genetics , Myelin Sheath/physiology , Myelin-Associated Glycoprotein , Nerve Regeneration , Rats , Sciatic Nerve/physiology , Transcription, Genetic
9.
Toxicol Appl Pharmacol ; 108(3): 428-35, 1991 May.
Article in English | MEDLINE | ID: mdl-1708532

ABSTRACT

Trimethyltin (TMT) is an alkyltin that targets neurons of the limbic system. A gene probe (i.e., mRNA) for myelin basic protein (MBP), a major component of central nervous system myelin, was used to monitor this toxic neuropathy in Sprague-Dawley rats. Animals were administered a single intraperitoneal injection of TMT-hydroxide at a neuropathic (8.0 mg/kg/body wt) or nonneuropathic (0.8 mg/kg/body wt) dose and sampled at 1, 3, or 7 days postexposure to correlate the progression of hippocampal neuropathology with probe (i.e., MBP-mRNA) levels. Microscopic examination of the brain showed only moderate but progressive damage over the 7-day postexposure period in animals treated with the neuropathic dose. Neuronal loss was first observed in the dendate gyrus and CA4 at 1 day postexposure, and progressed to the CA3c sector at 3 and 7 days postexposure. Elsewhere in the brain, minimal involvement of the entorhinal cortex neurons occurred 3 days postexposure and intensified by 7 days. No histological damage was seen at the nonneuropathic (0.8 mg/kg) dose. For gene probe analysis, the brain was divided into anterior and posterior halves. In rats treated with the neuropathic dose of TMT, the anterior brain showed progressive depressions of MBP-mRNA levels over the 1-, 3-, and 7-day postexposure period that correlated with increasing hippocampal neuropathology. The posterior brain showed no significant changes in MBP-mRNA levels with respect to that of controls over the same time period. At the nonneuropathic dose (0.8 mg/kg) a significant depression of MBP-mRNA levels occurred in the anterior brain at 7 days postexposure in the absence of overt histological damage.


Subject(s)
Myelin Basic Protein , Nervous System/drug effects , RNA, Messenger , Trimethyltin Compounds/toxicity , Animals , Blotting, Northern , DNA Probes , Hippocampus/drug effects , Hippocampus/pathology , Male , Nucleic Acid Hybridization , RNA, Messenger/analysis , Rats , Rats, Inbred Strains
10.
Neurotoxicology ; 12(4): 715-32, 1991.
Article in English | MEDLINE | ID: mdl-1724557

ABSTRACT

Cumulative exposure to the neurotoxicant acrylamide produces axonal damage in the distal ends of both central (CNS) and peripheral (PNS) nerve fibers and subsequent hind-limb paralysis. The messenger RNA which codes for the PNS myelin glycoprotein P0 (P0-mRNA) was used to monitor this toxic neuropathy in Sprague Dawley rats prior to, concurrent with, and subsequent to, ultrastructurally and immunocytochemically defined nerve damage. Rats were dosed every other day with acrylamide (50 mg/kg, IP) and sampled intermittently throughout a 4 week exposure period. Slot blot and Northern gel analyses of the proximal and distal sciatic nerve were used to determine a quantitated measure of P0-mRNA. Twenty-four hours after the first treatment, in the absence of ultrastructural damage, P0-mRNA increased 55% over control levels in the distal sciatic nerve. After 12 treatments, and concomitant with the appearance of spinal cord and PNS neuropathic damage and hindlimb dysfunction, P0-mRNA decreased 45% below control levels. Levels of P0-mRNA from rats exposed to 12 treatments of acrylamide but allowed to recover for 40 days, returned to 79% of control values to reflect the regeneration and remyelination occurring in the distal sciatic nerve. In spite of these fluctuations in levels of P0-mRNA, immunocytochemical staining of P0 protein in plastic sections of the distal sciatic nerve was present throughout all sample times. These results suggest that changes in neural specific mRNAs are sensitive to neurotoxic damage and can be used to monitor the pathogenesis of nerve degeneration.


Subject(s)
Acrylamides/toxicity , Axons/drug effects , Glycoproteins/genetics , Myelin Proteins/genetics , Myelin Sheath/drug effects , Peripheral Nerves/drug effects , RNA, Messenger/analysis , Acrylamide , Animals , Blotting, Northern , DNA Probes , Immunoenzyme Techniques , Male , Microscopy, Electron , Myelin P0 Protein , Nerve Regeneration/physiology , Nucleic Acid Hybridization , Rats , Rats, Inbred Strains
11.
Neurotoxicology ; 12(2): 265-76, 1991.
Article in English | MEDLINE | ID: mdl-1720231

ABSTRACT

Triethyltin (TET) is a neurotoxicant that produces severe but transient cerebral edema, characterized ultrastructurally by vacuolation of the intraperiod line of central nervous system (CNS) myelin. TET has been reported to depress levels of myelin basic protein (MBP), a protein thought to play a critical role in myelin compaction. In the present study, the genomic expression (i.e., mRNA) of MBP was monitored throughout the pathogenesis of TET-induced myelin edema and recovery in Sprague-Dawley rats given a single injection of a neuropathic (8.0 mg/kg) or non-neuropathic (0.8 mg/kg) dose of TET-bromide. Levels of MBP-mRNA from the anterior and posterior brain were collected 1 hr, 3 hr, 2d, and 7d, postexposure. The optic nerve and caudal brainstem, representing anterior and posterior brain sites, respectively, were examined at the same time-points for ultrastructural evidence of edema and recovery. Our data indicate that neuropathic doses (8.0 mg/kg) of TET significantly stimulated MBP transcript throughout the brain at all exposure time-points. The magnitude and time-course of this stimulation differed in the anterior and posterior brain, with the latter region showing higher levels of MBP-mRNA. In the posterior brain, the highest levels of mRNA correlated with the appearance of edema in the caudal brainstem. In the anterior brain, MBP-mRNA levels were only marginally increased over controls. Ultrastructural evidence of myelin edema was confined to the brainstem in rats treated with neuropathic dose of TET. Intralamellar vacuolation appeared at 3 hr and 2d postexposure and could be correlated with peak levels of MBP transcript, whereas, recompacted myelin, which appeared by 7d postexposure, was associated with declining levels of the mRNA. Ultrastructural changes in the oligodendroglia were suggestive of metabolic stimulation and correlated with high MBP-mRNA levels. In summary, these data indicate that an initial genomic event in TET-induced myelin edema is stimulation of MBP transcript.


Subject(s)
Edema/metabolism , Myelin Basic Protein/metabolism , Myelin Sheath , RNA, Messenger/biosynthesis , Triethyltin Compounds/toxicity , Animals , Blotting, Northern , Central Nervous System Diseases/chemically induced , Central Nervous System Diseases/genetics , Central Nervous System Diseases/metabolism , DNA/genetics , DNA Probes , Edema/chemically induced , Edema/genetics , Male , Myelin Basic Protein/genetics , Nucleic Acid Hybridization , Rats , Rats, Inbred Strains
12.
Dev Neurosci ; 12(1): 22-33, 1990.
Article in English | MEDLINE | ID: mdl-1688760

ABSTRACT

The distal segments of the crush-injured and permanently transected sciatic nerve provide models to study Schwann cell activity in the presence and absence of Schwann cell-axonal contact, respectively. We examined the quantity and quality of transcript coding for the myelin-associated glycoprotein (MAG) over a 3-week period following crush injury and at 35 days after transection to investigate possible regulation of this gene during nerve injury and subsequent repair. Northern blot and slot blot analysis indicated a sharp decrease in levels of MAG mRNA 2 days after crush injury which was followed by a progressive increase in levels of message between 7 and 21 days after injury. Western blot analysis showed that levels of MAG protein decreased substantially 7 days after crush injury, which returned to 70% of the adult value by 21 days after injury. MAG mRNA and protein were undetectable by Northern and Western analysis, respectively, in the distal segment of the sciatic nerve 35 days after permanent transection. This infers distinct down-regulation of MAG gene expression after permanent transection of a peripheral nerve. These comparative studies of MAG transcripts and encoded protein may indicate regulation of MAG gene expression at the level of transcription, and possibly at the level of post-transcription in these experimental models of peripheral neuropathies.


Subject(s)
Gene Expression Regulation , Myelin Proteins/genetics , Nerve Regeneration , Schwann Cells/physiology , Sciatic Nerve/metabolism , Animals , Myelin Proteins/metabolism , Myelin-Associated Glycoprotein , RNA, Messenger/metabolism , Rats , Rats, Inbred Strains , Schwann Cells/metabolism , Sciatic Nerve/cytology
13.
J Cell Biol ; 109(3): 1245-56, 1989 Sep.
Article in English | MEDLINE | ID: mdl-2504730

ABSTRACT

The expression of the apolipoprotein A-I (apo A-I) gene was investigated in the myelinating sciatic nerve. Hybridization analysis with an apo A-I cDNA probe obtained from a cDNA library of mRNA isolated from rapidly myelinating chick sciatic nerve indicated that apo A-I coding transcripts increase during development in the chick sciatic nerve in parallel with the increase of myelin lamellae. Substantial apo A-I-like immunoreactivity in chick sciatic nerve homogenates was detected by Western blotting. The amount of antigen increased from the 15-d embryonic stage to 1 d posthatch and then decreased. Two subcellular fractions corresponding to the cytoplasmic compartments were particularly enriched in apo A-I. apo A-I immunoreactivity was also found in highly purified myelin preparations. Immunohistochemical staining provided further evidence for the presence of apo A-I in the endoneurial compartment of the sciatic nerve. Electron microscopic examination of these fractions after negative staining showed the presence of spherical and disc-shaped particles resembling high density lipoproteins. The presence of apo A-I, cholesterol esters, phospholipids, and triacylglycerols in ultracentrifugal fractions corresponding to serum lipoproteins and the behavior of apo A-I on nondenaturing gradient gels implied that apo A-I was associated with lipid. Studies with short-term organ cultures of sciatic nerves from 1-d chicks strengthened the evidence for local synthesis and secretion of apo A-I and apo A-I-containing lipoproteins by this tissue. These results establish that the apo A-I gene is actively expressed in developing sciatic nerve during the period of rapid myelination. These findings support the hypothesis that apo A-I synthesized within the nerve participates in the local transport of lipids used in myelin biosynthesis.


Subject(s)
Apolipoproteins A/genetics , Genes , Lipoproteins, HDL/genetics , Nerve Fibers, Myelinated/metabolism , RNA, Messenger/genetics , Sciatic Nerve/growth & development , Transcription, Genetic , Aging , Animals , Apolipoprotein A-I , Apolipoproteins A/biosynthesis , Chick Embryo , Chickens , DNA/genetics , DNA/isolation & purification , Immunohistochemistry , Nerve Fibers, Myelinated/ultrastructure , Organ Culture Techniques , Sciatic Nerve/metabolism , Subcellular Fractions/metabolism
14.
Brain Res ; 464(2): 133-41, 1988 Sep.
Article in English | MEDLINE | ID: mdl-2464407

ABSTRACT

The crush-injured sciatic nerve provides a model to study Schwann cell regulation of myelin gene expression during the process of demyelination and remyelination. In order to investigate the possible transcriptional regulation of myelin gene expression, the quantity, quality and translational efficiency of PO (the major myelin glycoprotein) and MBP (the myelin basic proteins) coding messages were investigated as a function of time following crush-injury of the adult rat sciatic nerve. Northern blot analysis indicated that the size of the PO and MBP transcripts remain unchanged in the distal segments of crushed sciatic nerves at 1, 2, 4, 7, 10, 14 and 21 days after crush-injury. Dot-blot analysis showed a sharp drop in levels of PO and MBP coding transcripts 1 day after crush-injury with the lowest steady-state levels at 4-7 days. Message levels were found to increase after 7 days, the highest increase in levels of message was found to be between 10 and 14 days. The highest steady-state level of both transcripts was observed at 21 days. In vitro translation and immunoprecipitation of PO-translated products from various stages of crush-injury also indicated this trend. The pattern of gene expression of PO- and MBP-coding transcripts parallel each other and follow the pattern of demyelination and remyelination. The results are also consistent with our previous interpretation which suggests that PO and MBP gene expression is regulated at the level of transcription and that these two genes might be coordinately expressed. Western blot analysis of PO protein from these stages revealed a similar decrease and then increase in the levels of the protein.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Gene Expression Regulation , Genes , Myelin Proteins/genetics , Sciatic Nerve/injuries , Transcription, Genetic , Adult , Animals , Blotting, Northern , Humans , Myelin P0 Protein , Poly A/genetics , Poly A/isolation & purification , RNA/genetics , RNA/isolation & purification , RNA, Messenger/genetics , RNA, Messenger/isolation & purification , Rats , Reference Values , Sciatic Nerve/metabolism , Time Factors
15.
Neurochem Res ; 12(4): 377-84, 1987 Apr.
Article in English | MEDLINE | ID: mdl-2439933

ABSTRACT

The major protein (PO) in PNS myelin is an integral membrane glycoprotein with a molecular weight of about 30 K. The level of PO protein in the developing sciatic nerve of the chicken was monitored by a solid-phase immunoassay and densitometry of Coomassie blue stained polyacrylamide gels. The most rapid rate of accumulation of PO protein occurred after 16 days of embryonic development. In addition to the 30 K PO protein, a number of higher molecular weight proteins could be distinctly detected by immunoblotting. Amongst these high molecular weight proteins, a species with an apparent molecular weight of 42 K was specifically immunostained with epitope-selected polyclonal antibodies against PO protein. This 42 K protein could be first detected after 16 days of embryonic development and increased rapidly following the pattern of myelination in the sciatic nerve. The enzyme endoglycosidase F, which specifically removes N-asparagine linked high mannose and complex carbohydrates from glycoproteins, converted the PO and 42 K proteins to lower molecular weight forms, which could be specifically immunostained by epitope selected polyclonal antibodies to the PO protein. Subcellular fractionation of the 17-day embryonic nerve demonstrated that the 42 K protein was enriched in myelin and microsomal subfractions relative to the total homogenate. These results indicate that the 42 K immuno-crossreactive protein might be chemically and functionally related to the PO protein of the PNS myelin.


Subject(s)
Myelin Proteins/analysis , Peripheral Nerves/analysis , Animals , Cell Fractionation , Chickens , Epitopes/analysis , Molecular Weight , Myelin P0 Protein , Myelin Proteins/immunology , Sciatic Nerve/analysis
16.
Brain Res ; 388(1): 57-67, 1987 Apr.
Article in English | MEDLINE | ID: mdl-2438000

ABSTRACT

Regulation of myelin protein gene expression in the presence and absence of myelin assembly can be assessed using crushed or permanently transected adult sciatic nerves of rats. The P0 glycoprotein and the myelin basic protein (MBP) are the major myelin-specific proteins of the peripheral nervous system. The steady-state level of P0 and MBP messenger RNA was determined by dot-blot analysis of poly(A)+ RNA from crushed and transected nerves of rats at 35 days post operation. The rat P0-specific cDNA clone, pSN63c, and mouse MBP-specific cDNA clone, pHF43, were used as probes. The level and quality of the poly(A)+ RNA was assessed by in vitro translation and immunoprecipitation of the translation products with anti-chick P0 antibody. Comparison of the steady-state level of P0 and MBP transcripts and the level of anti-P0 immunoprecipitated translation products from RNA extracts of permanently transected, crushed, adult control and 21-day-old control rat nerves indicated that the level of P0 and MBP messages was significantly reduced in the permanently transected model, whereas it was restored to normal in the crushed sciatic nerve 35 days post injury. These results suggest that regulation of P0 and MBP gene expression most likely occurs at the transcriptional or post-transcriptional level in the two models of peripheral neuropathies. Northern blot analysis indicated the absence of differential splicing of the message in crushed or transected nerves. The experiments also indicate that these two important gene products required for myelin synthesis and assembly seem to be co-regulated. However, the data do not rule out the possibility that regulation of gene expression may also occur at the level of translation or post-translational processing.


Subject(s)
Gene Expression Regulation , Myelin Proteins/genetics , Myelin Sheath/physiology , Peripheral Nerves/physiology , RNA, Messenger/analysis , Animals , Cloning, Molecular , DNA , Myelin P0 Protein , Nerve Regeneration , Protein Biosynthesis , Rats
18.
Comp Biochem Physiol B ; 87(4): 895-905, 1987.
Article in English | MEDLINE | ID: mdl-2444388

ABSTRACT

1. The mammalian PO gene exhibits low homology to the avian PO gene and transcript. 2. The avian PO mRNA is smaller than the mammalian mRNA. 3. The primary structure of mammalian and avian PO proteins differ in their molecular weight, isoelectric point, and chymotryptic peptide pattern. 4. Similarity between the PO proteins is indicated by immuno-cross-reactivity of the anti-chicken PO IgG to mammalian PO proteins. 5. Similarities at the level of amino acid sequence could provide insight on the structure and function of the PO protein.


Subject(s)
Brain/metabolism , Myelin Proteins/genetics , Myelin Sheath/metabolism , Sciatic Nerve/metabolism , Animals , Chickens , Genes , Myelin P0 Protein , Nucleic Acid Hybridization , Organ Specificity , Poly A/genetics , Protein Biosynthesis , RNA/genetics , RNA, Messenger , Rats , Species Specificity
19.
Brain Res ; 352(2): 302-5, 1985 Jun.
Article in English | MEDLINE | ID: mdl-2411357

ABSTRACT

Poly(A+)RNA from sciatic nerves of embryos and chicks was translated in a rabbit reticulocyte cell-free system. The 30-K mol. wt. PO protein which is the major and specific protein constituent of peripheral nervous system myelin was used as a marker of myelin synthesis in the preparations. Immunoprecipitation of total translation products with rabbit anti-PO protein antibody showed the presence of a 29K protein band on the autoradiograms. The intensity of this specific immunoprecipitated band increased significantly from very low levels with RNA from the 15-day embryonic nerve to a maximum with extracts from 1-day-old chicks. This increase parallels that of the rapid deposition of the PO protein in the developing sciatic nerve in vivo. The experiments demonstrate for the first time, that it is possible to show synthesis of PO protein in vitro using exogenous RNA as the template.


Subject(s)
Myelin Proteins/genetics , Peripheral Nerves/metabolism , Protein Biosynthesis , RNA, Messenger/metabolism , Animals , Chick Embryo , Chickens , Myelin P0 Protein , Myelin Proteins/biosynthesis , RNA, Messenger/isolation & purification , Rabbits , Reticulocytes/metabolism
20.
Muscle Nerve ; 8(2): 120-4, 1985 Feb.
Article in English | MEDLINE | ID: mdl-2414650

ABSTRACT

To investigate whether various myelin markers could detect pathological changes in myelination, the activity of 2'-3'-cyclic nucleotide 3'-phosphodiesterase (CNP) and the level of PO protein were compared in the peripheral nervous system (PNS) of the dystrophic mouse and chicken and their phenotypically normal siblings. The same comparison was made for subcellular fractions of these nerves. The level of PO protein and the activity of CNP were normal in the spinal roots of sciatic nerves of the 129B6F1/Jdy/dy strain of dystrophic mouse. These parameters were slightly but significantly lower in the spinal roots of the 129REJ/dy/dy strain of dystrophic mouse. These results suggest that the 129B6F1/Jdy/dy mutant and the 129REJ/dy/dy mutant mouse might not have the same type of biochemical abnormality in their PNS. The specific activity of CNP and the proportion of PO protein increased significantly in the various regions of the PNS of 1-day-old chicks when compared to that of the 18-day-old embryos. Subcellular fractionation of peripheral nerves indicated that these components were enriched in the crude myelin fraction. These results support the conclusion that PO protein and CNP are suitable markers of myelinogenesis in the PNS of the chick. These parameters were normal in the line 413 dystrophic chicken. These results do not support the conclusion of a systemic membrane defect in the PNS of the dystrophic mouse and chicken.


Subject(s)
2',3'-Cyclic-Nucleotide Phosphodiesterases/metabolism , Muscular Dystrophies/metabolism , Myelin Proteins/metabolism , Phosphoric Diester Hydrolases , 2',3'-Cyclic Nucleotide 3'-Phosphodiesterase , Animals , Chickens , Mice , Mice, Mutant Strains , Muscular Dystrophies/genetics , Muscular Dystrophies/physiopathology , Myelin P0 Protein , Myelin Sheath/physiology , Peripheral Nerves/physiopathology , Subcellular Fractions/metabolism
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