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1.
Ann Thorac Surg ; 110(6): 1909-1916, 2020 12.
Article in English | MEDLINE | ID: mdl-32504601

ABSTRACT

BACKGROUND: Learning curves and skill attrition with aging have been reported to impair outcomes in select surgical subspecialties, but their role in complex cardiac surgery remains unknown. METHODS: From 1986 to 2019, 2314 patients underwent reoperative cardiac surgery: coronary artery bypass grafting (n = 543), valve (n = 1527), or combined coronary artery bypass grafting and valve (n = 244). Thirty-four different surgeons in practice between 1 and 39 years were included. Standardized mortality ratio (observed-to-expected) was determined for all surgeons in each post-training year of experience. RESULTS: Risk-adjusted cumulative sum change-point analysis was used to define five distinct career phases: 0 to 4 years, 5 to 8 years, 9 to 17 years, 18 to 28 years, and 29 to 39 years. With 5 to 8 years and 18 to 28 years of experience, standardized mortality ratio was near unity (0.95 and 1.05, respectively) and lowest with 9 to 17 years of experience (0.78, P = .03). In the youngest experience group (0 to 4 years), observed and expected mortality were both highest, and standardized mortality ratio was elevated at 1.29, which approached statistical significance (P = .059). In the oldest experience group (29 to 39 years), expected mortality was low compared with most other groups but observed mortality increased, yielding a significantly elevated standardized mortality ratio at 1.53 (P = .032). CONCLUSIONS: Standardized mortality ratios with reoperative cardiac surgery were highest early and late in a surgeon's career and lowest in mid career. As surgeons gain experience, outcomes improve through the first two career decades, then stabilize in the third decade before declining in the fourth decade.


Subject(s)
Clinical Competence , Coronary Artery Bypass/mortality , Heart Valve Prosthesis Implantation/mortality , Postoperative Complications/epidemiology , Reoperation/mortality , Aged , Aged, 80 and over , Coronary Artery Bypass/adverse effects , Coronary Artery Bypass/statistics & numerical data , Heart Valve Prosthesis Implantation/adverse effects , Heart Valve Prosthesis Implantation/statistics & numerical data , Hospital Mortality , Humans , Learning Curve , Middle Aged , Time Factors
2.
Geriatr Gerontol Int ; 18(1): 42-49, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28762596

ABSTRACT

AIM: To determine whether home-based exercise can improve clinical outcomes in older patients with advanced chronic obstructive pulmonary disease using long-term oxygen therapy. METHODS: Information was provided to improve chronic obstructive pulmonary disease self-management before the onset of the present prospective 3-year cohort study. Patients selected either home-based exercise using a lower-limb cycle machine (ergo-bicycle; group E), or usual exercise (group U). To assess self-management, the Lung Information Needs Questionnaire was evaluated every 6 months. Clinical outcomes included the 6-min walk test, pulmonary function tests, the body mass index, airflow obstruction, dyspnea and exercise index, St. George's respiratory questionnaire, and the number of exacerbations and hospitalizations. RESULTS: A total of 136 patients (group E = 72; group U = 64), with a mean age of 74.2 years were enrolled. Total Lung Information Needs Questionnaire scores improved over 3 years for group E (P = 0.003). The distance of the 6-min walk test was well maintained in group E, but significantly decreased in group U (P < 0.001). The percentage of forced expiratory volume in 1 s at baseline was lower in group E (P = 0.016), but was maintained over 3 years, whereas a significant reduction was seen in group U (P = 0.001). The body mass index, airflow obstruction, dyspnea and exercise index significantly worsened in both groups over 3 years (group E: P = 0.011; group U: P < 0.001), whereas a significant decrease in the number of exacerbations was noted in group E (P = 0.009). CONCLUSIONS: Patients who undertook home-based exercise using an ergo-bicycle were able to maintain clinical outcomes including 6-min walk test distance and percentage of forced expiratory volume in 1 s predicted, and recorded fewer exacerbations over 3 years. Geriatr Gerontol Int 2018; 18: 42-49.


Subject(s)
Exercise Therapy , Home Care Services , Pulmonary Disease, Chronic Obstructive/therapy , Aged , Humans , Prospective Studies , Treatment Outcome
3.
J Neurochem ; 142(3): 378-391, 2017 08.
Article in English | MEDLINE | ID: mdl-28512742

ABSTRACT

Differentiation of oligodendroglial progenitor cells (OPCs) into myelinating oligodendrocytes is known to be regulated by the microenvironment where they differentiate. However, current research has not verified whether or not oligodendroglial lineage cells (OLCs) derived from different anatomical regions of the central nervous system (CNS) respond to microenvironmental cues in the same manner. Here, we isolated pure OPCs from rat neonatal forebrain (FB) and spinal cord (SC) and compared their phenotypes in the same in vitro conditions. We found that although FB and SC OLCs responded differently to the same external factors; they were distinct in proliferation response to mitogens, oligodendrocyte phenotype after differentiation, and cytotoxic responses to α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate-type glutamate receptor-mediated excitotoxicity at immature stages of differentiation in a cell-intrinsic manner. Moreover, transcriptome analysis identified genes differentially expressed between these OPC populations, including those encoding transcription factors (TFs), cell surface molecules, and signaling molecules. Particularly, FB and SC OPCs retained the expression of FB- or SC-specific TFs, such as Foxg1 and Hoxc8, respectively, even after serial passaging in vitro. Given the essential role of these TFs in the regional identities of CNS cells along the rostrocaudal axis, our results suggest that CNS region-specific gene regulation by these TFs may cause cell-intrinsic differences in cellular responses between FB and SC OLCs to extracellular molecules. Further understanding of the regional differences among OPC populations will help to improve treatments for demyelination in different CNS regions and to facilitate the development of stem cell-derived OPCs for cell transplantation therapies for demyelination. Cover Image for this issue: doi. 10.1111/jnc.13809.


Subject(s)
Cell Differentiation/physiology , Cell Lineage/physiology , Neurons/cytology , Oligodendroglia/cytology , Prosencephalon/cytology , Stem Cells/cytology , Animals , Cells, Cultured , Demyelinating Diseases/metabolism , Gene Expression Regulation/physiology , Oligodendroglia/metabolism , Prosencephalon/metabolism , Rats
4.
J Card Surg ; 32(2): 159-161, 2017 Feb.
Article in English | MEDLINE | ID: mdl-28076895

ABSTRACT

Left ventricular noncompaction (LVNC) may result in systolic left ventricular (LV) failure resulting in the need for heart transplantation. LV assist devices (LVAD) have been used to bridge these patients to transplantation; however, the extensive trabeculations found in these patients predispose them to thromboembolic events and pump thrombosis. We describe a patient with LVNC in whom an aggressive surgical approach was used to debride the LV cavity of trabeculations to successfully implant an LVAD.


Subject(s)
Cardiac Surgical Procedures/methods , Cardiomyopathies/surgery , Heart Ventricles/surgery , Heart-Assist Devices , Ventricular Function, Left/physiology , Adult , Cardiomyopathies/diagnosis , Cardiomyopathies/physiopathology , Echocardiography , Female , Heart Ventricles/diagnostic imaging , Heart Ventricles/physiopathology , Humans , Tomography, X-Ray Computed
5.
J Neurosci ; 34(32): 10729-42, 2014 Aug 06.
Article in English | MEDLINE | ID: mdl-25100604

ABSTRACT

Motoneuron death after transection of the axons (axotomy) in neonates is believed to share the same mechanistic bases as naturally occurring programmed cell death during development. The c-Jun N-terminal kinase pathway is activated in both forms of motoneuron death, but it remains unknown to what extent these two forms of motoneuron death depend on this pathway and which upstream kinases are involved. We found that numbers of facial motoneurons are doubled in neonatal mice deficient in either ZPK/DLK (zipper protein kinase, also known as dual leucine zipper kinase), a mitogen-activated protein kinase kinase kinase, or in MKK4/MAP2K4, a mitogen-activated protein kinase kinase directly downstream of ZPK/DLK, and that the facial motoneurons in those mutant mice are completely resistant to axotomy-induced death. Conditional deletion of MKK4/MAP2K4 in neurons further suggested that ZPK/DLK and MKK4/MAP2K4-dependent mechanisms underlying axotomy-induced death are motoneuron autonomous. Nevertheless, quantitative analysis of facial motoneurons during embryogenesis revealed that both ZPK/DLK and MKK4/MAP2K4-dependent and -independent mechanisms contribute to developmental elimination of excess motoneurons. In contrast to MKK4/MAP2K4, mice lacking MKK7/MAP2K7, another mitogen-activated protein kinase kinase directly downstream of ZPK/DLK, conditionally in neurons did not have excess facial motoneurons. However, some MKK7/MAP2K7-deficient facial motoneurons were resistant to axotomy-induced death, indicating a synergistic effect of MKK7/MAP2K7 on axotomy-induced death of these facial motoneurons. Together, our study provides compelling evidence for the pivotal roles of the ZPK/DLK and MKK4/MAP2K4-dependent mechanism in axotomy-induced motoneuron death in neonates and also demonstrates that axotomy-induced motoneuron death is not identical to developmental motoneuron death with respect to the involvement of ZPK/DLK, MKK4/MAP2K4 and MKK7/MAP2K7.


Subject(s)
Central Nervous System/pathology , Facial Nerve Injuries/pathology , MAP Kinase Kinase 4/metabolism , MAP Kinase Kinase Kinases/metabolism , Signal Transduction/physiology , Animals , Animals, Newborn , Axotomy/adverse effects , Calcium-Binding Proteins/metabolism , Cell Death/physiology , Central Nervous System/growth & development , Central Nervous System/metabolism , Choline O-Acetyltransferase/metabolism , Dextrans , Disease Models, Animal , Facial Nerve Injuries/metabolism , Gene Expression Regulation, Developmental/genetics , Gene Expression Regulation, Developmental/physiology , MAP Kinase Kinase 4/genetics , MAP Kinase Kinase Kinases/genetics , Mice , Mice, Transgenic , Microfilament Proteins/metabolism , Nestin/genetics , Nestin/metabolism , Phosphopyruvate Hydratase/metabolism , Proto-Oncogene Proteins c-jun/metabolism , Rhodamines , Signal Transduction/genetics
6.
J Neuroinflammation ; 9: 227, 2012 Sep 28.
Article in English | MEDLINE | ID: mdl-23020843

ABSTRACT

BACKGROUND: Recent fate-mapping studies establish that microglia, the resident mononuclear phagocytes of the CNS, are distinct in origin from the bone marrow-derived myeloid lineage. Interferon regulatory factor 8 (IRF8, also known as interferon consensus sequence binding protein) plays essential roles in development and function of the bone marrow-derived myeloid lineage. However, little is known about its roles in microglia. METHODS: The CNS tissues of IRF8-deficient mice were immunohistochemically analyzed. Pure microglia isolated from wild-type and IRF8-deficient mice were studied in vitro by proliferation, immunocytochemical and phagocytosis assays. Microglial response in vivo was compared between wild-type and IRF8-deficient mice in the cuprizon-induced demyelination model. RESULTS: Our analysis of IRF8-deficient mice revealed that, in contrast to compromised development of IRF8-deficient bone marrow myeloid lineage cells, development and colonization of microglia are not obviously affected by loss of IRF8. However, IRF8-deficient microglia demonstrate several defective phenotypes. In vivo, IRF8-deficient microglia have fewer elaborated processes with reduced expression of IBA1/AIF1 compared with wild-type microglia, suggesting a defective phenotype. IRF8-deficient microglia are significantly less proliferative in mixed glial cultures than wild-type microglia. Unlike IRF8-deficient bone marrow myeloid progenitors, exogenous macrophage colony stimulating factor (colony stimulating factor 1) (M-CSF (CSF1)) restores their proliferation in mixed glial cultures. In addition, IRF8-deficient microglia exhibit an exaggerated growth response to exogenous granulocyte-macrophage colony stimulating factor (colony stimulating factor 2) (GM-CSF (CSF2)) in the presence of other glial cells. IRF8-deficient microglia also demonstrate altered cytokine expressions in response to interferon-gamma and lipopolysaccharide in vitro. Moreover, the maximum phagocytic capacity of IRF8-deficient microglia is reduced, although their engulfment of zymosan particles is not overtly impaired. Defective scavenging activity of IRF8-deficient microglia was further confirmed in vivo in the cuprizone-induced demyelination model in mice. CONCLUSIONS: This study is the first to demonstrate the essential contribution of IRF8-mediated transcription to a broad range of microglial phenotype. Microglia are distinct from the bone marrow myeloid lineage with respect to their dependence on IRF8-mediated transcription.


Subject(s)
Interferon Regulatory Factors/physiology , Microglia/metabolism , Phenotype , Animals , Animals, Newborn , Antigens, CD/metabolism , Antigens, Differentiation, Myelomonocytic/metabolism , Brain/cytology , CD11b Antigen/metabolism , Calcium-Binding Proteins/genetics , Calcium-Binding Proteins/metabolism , Cell Proliferation/drug effects , Cells, Cultured , Cuprizone/toxicity , Demyelinating Diseases/chemically induced , Disease Models, Animal , Flow Cytometry , Gene Expression Regulation/drug effects , Gene Expression Regulation/genetics , Interferon Regulatory Factors/deficiency , Interferon Regulatory Factors/metabolism , Mice , Mice, Inbred C57BL , Mice, Knockout , Microfilament Proteins/genetics , Microfilament Proteins/metabolism , Monoamine Oxidase Inhibitors/toxicity , Myelin Sheath/pathology , Phagocytosis/genetics , Phenylurea Compounds/pharmacology , Spinal Cord/metabolism , Spinal Cord/pathology
7.
Neurobiol Aging ; 33(3): 499-509, 2012 Mar.
Article in English | MEDLINE | ID: mdl-20594620

ABSTRACT

Accumulating evidence indicates that white matter degeneration contributes to the neural disconnections that underlie Alzheimer's disease pathophysiology. Although this white matter degeneration is partly attributable to axonopathy associated with neuronal degeneration, amyloid ß (Aß) protein-mediated damage to oligodendrocytes could be another mechanism. To test this hypothesis, we studied effects of soluble Aß in oligomeric form on survival and differentiation of cells of the oligodendroglial lineage using highly purified oligodendroglial cultures from rats at different developmental stages. Aß oligomer at 10 µM or higher reduced survival of mature oligodendrocytes, whereas oligodendroglial progenitor cells (OPCs) were relatively resistant to the Aß oligomer-mediated cytotoxicity. Further study revealed that Aß oligomer even at 1 µM accelerated 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) formazan exocytosis in mature oligodendrocytes, and, more significantly, inhibited myelin sheet formation after induction of in vitro differentiation of OPCs. These results imply a novel pathogenetic mechanism underlying Aß oligomer-mediated white matter degeneration, which could impair myelin maintenance and remyelination by adult OPCs, resulting in accumulating damage to myelinating axons thereby contributing to neural disconnections.


Subject(s)
Alzheimer Disease/metabolism , Amyloid beta-Peptides/toxicity , Myelin Sheath/pathology , Peptide Fragments/toxicity , Stem Cells/drug effects , Wallerian Degeneration/metabolism , Alzheimer Disease/etiology , Alzheimer Disease/pathology , Amyloid beta-Peptides/metabolism , Animals , Animals, Newborn , Myelin Sheath/drug effects , Nerve Fibers, Myelinated/metabolism , Nerve Fibers, Myelinated/pathology , Oligodendroglia/drug effects , Oligodendroglia/pathology , Peptide Fragments/metabolism , Primary Cell Culture , Rats , Rats, Inbred Lew , Stem Cells/pathology , Tumor Cells, Cultured , Wallerian Degeneration/pathology
8.
Tissue Eng Part A ; 17(23-24): 2931-42, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21882895

ABSTRACT

Fibrin is a promising matrix for use in promoting nerve repair given its natural occurrence in peripheral nerve injuries, and the biophysical properties of this matrix can be regulated to modulate tissue regeneration. In this study, we examined the effect of physical and mechanical properties of fibrin gels on dorsal root ganglia (DRG) neurite extension. Increases in fibrinogen concentration increased the number of fibrin strands, resulting in decreased pore size and increased stiffness. Neurite extension was reduced when DRG explants were cultured within fibrin gels of increasing fibrinogen concentrations (from 9.5 to 141 mg/mL). The addition of NaCl also increased the number of fibrin strands, reducing fiber diameter and porosity, while increasing mechanical strength, and reductions in neurite extension correlated with increases in NaCl content. We determined that neurite extension within fibrin gels is dependent on fibrinolysis and is mediated by the secretion of serine proteases and matrix metalloproteinases by entrapped DRGs, as confirmed by culturing cells in the presence of inhibitors against these enzymes and real-time-polymerase chain reaction. Taken together, the results of this study provide new insight into the effect of fibrin gel biophysical properties on neurite extension and suggest new opportunities to improve the efficacy of these materials when used as nerve guidance conduits.


Subject(s)
Fibrin/pharmacology , Gels/pharmacology , Mechanical Phenomena/drug effects , Neurites/drug effects , Neurites/metabolism , Animals , Fibrin/ultrastructure , Fibrinogen/pharmacology , Ganglia, Spinal/drug effects , Ganglia, Spinal/growth & development , Humans , Matrix Metalloproteinase Inhibitors , Matrix Metalloproteinases/genetics , Matrix Metalloproteinases/metabolism , Mice , Mice, Inbred C57BL , Protease Inhibitors/pharmacology , Proteolysis/drug effects , Serine Proteases/genetics , Serine Proteases/metabolism , Sodium Chloride/pharmacology , Time Factors
9.
J Magn Reson Imaging ; 34(5): 1080-91, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21932362

ABSTRACT

PURPOSE: To establish the correspondence between the two histologically observable and diffusion tensor MRI (DTMRI) measurements of myolaminae orientation for the first time and show that single myolaminar orientations observed in local histology may result from histological artifact. MATERIALS AND METHODS: DTMRI was performed on six sheep left ventricles (LV), then corresponding direct histological transmural measurements were made within the anterobasal and lateral-equatorial LV. Secondary and tertiary eigenvectors of the diffusion tensor were compared with each of the two locally observable sheet orientations from histology. Diffusion tensor invariants were calculated to compare differences in microstructural diffusive properties between histological locations with one observable sheet population and two observable sheet populations. RESULTS: Mean difference ± 1SD between DTMRI and histology measured sheet angles was 8° ± 27°. Diffusion tensor invariants showed no significant differences between histological locations with one observable sheet population and locations with two observable sheet populations. CONCLUSION: DTMRI measurements of myolaminae orientations derived from the secondary and tertiary eigenvectors correspond to each of the two local myolaminae orientations observed in histology. Two local sheet populations may exist throughout LV myocardium, and one local sheet population observed in histology may be a result of preparation artifact.


Subject(s)
Diffusion Magnetic Resonance Imaging/methods , Heart Ventricles/pathology , Myocardium/pathology , Algorithms , Animals , Artifacts , Image Processing, Computer-Assisted , Male , Models, Anatomic , Models, Statistical , Reproducibility of Results , Sheep
10.
J Neurosci ; 31(20): 7223-8, 2011 May 18.
Article in English | MEDLINE | ID: mdl-21593306

ABSTRACT

Activation of mitogen-activated protein kinase pathways is critically involved in naturally occurring programmed cell death of motoneurons during development, but the upstream mediators remain undetermined. We found that mice deficient in ZPK, also called DLK (ZPK/DLK), an upstream kinase in these pathways, have twice as many spinal motoneurons as do their wild-type littermates. Nuclear HB9/MNX1-positive motoneuron pools were generated similarly in the spinal cord of both ZPK/DLK-deficient and wild-type embryos. Thereafter, however, significantly less apoptotic motoneurons were found in ZPK/DLK-deficient embryos compared with wild-type embryos, resulting in retention of excess numbers of motoneurons after birth. Notably, these excess motoneurons remained viable without atrophic changes in the ZPK/DLK-deficient mice surviving into adulthood. Analysis of the diaphragm and the phrenic nerve revealed that clustering and innervation of neuromuscular junctions were indistinguishable between ZPK/DLK-deficient and wild-type mice, whereas the proximal portion of the phrenic nerve of ZPK/DLK-deficient mice contained significantly more axons than the distal portion. This result supports the hypothesis that some excess ZPK/DLK-deficient motoneurons survived without atrophy despite failure to establish axonal contact with their targets. This study provides compelling evidence for a critical role for ZPK/DLK in naturally occurring programmed cell death of motoneurons and suggests that ZPK/DLK could become a strategic therapeutic target in motor neuron diseases in which aberrant activation of the apoptogenic cascade is involved.


Subject(s)
Apoptosis/physiology , MAP Kinase Kinase Kinases/physiology , Motor Neurons/enzymology , Animals , Cell Death/physiology , Female , MAP Kinase Kinase Kinases/deficiency , Male , Mice , Mice, Knockout , Motor Neurons/cytology
11.
J Neuroinflammation ; 8: 8, 2011 Jan 24.
Article in English | MEDLINE | ID: mdl-21261980

ABSTRACT

BACKGROUND: Administration of exogenous interferon-γ (IFNγ) aggravates the symptoms of multiple sclerosis (MS), whereas interferon-ß (IFNß) is used for treatment of MS patients. We previously demonstrated that IFNγ induces apoptosis of oligodendroglial progenitor cells (OPCs), suggesting that IFNγ is more toxic to OPCs than IFNß. Thus we hypothesized that a difference in expression profiles between IFNγ-inducible and IFNß-inducible genes in OPCs would predict the genes responsible for IFNγ-mediated cytotoxic effects on OPCs. We have tested this hypothesis particularly focusing on the interferon regulatory factors (IRFs) well-known transcription factors up-regulated by IFNs. METHODS: Highly pure primary rat OPC cultures were treated with IFNγ and IFNß. Cell death and proliferation were assessed by MTT reduction, caspase-3-like proteinase activity, Annexin-V binding, mitochondrial membrane potential, and BrdU-incorporation. Induction of all nine IRFs was comprehensively compared by quantitative PCR between IFNγ-treated and IFNß-treated OPCs. IRFs more strongly induced by IFNγ than by IFNß were selected, and tested for their ability to induce OPC apoptosis by overexpression and by inhibition by dominant-negative proteins or small interference RNA either in the presence or absence of IFNγ. RESULTS: Unlike IFNγ, IFNß did not induce apoptosis of OPCs. Among nine IRFs, IRF1 and IRF8 were preferentially up-regulated by IFNγ. In contrast, IRF7 was more robustly induced by IFNß than by IFNγ. Overexpressed IRF1 elicited apoptosis of OPCs, and a dominant negative IRF1 protein partially protected OPCs from IFNγ-induced apoptosis, indicating a substantial contribution of IRF1 to IFNγ-induced OPC apoptosis. On the other hand, overexpression of IRF8 itself had only marginal proapoptotic effects. However, overexpressed IRF8 enhanced the IFNγ-induced cytotoxicity and the proapoptotic effect of overexpressed IRF1, and down-regulation of IRF8 by siRNA partially but significantly reduced preapoptotic cells after treatment with IFNγ, suggesting that IRF8 cooperatively enhances IFNγ-induced OPC apoptosis. CONCLUSIONS: This study has identified that IRF1 and IRF8 mediate IFNγ-signaling leading to OPC apoptosis. Therapies targeting at these transcription factors and their target genes could reduce IFNγ-induced OPC loss and thereby enhance remyelination in MS patients.


Subject(s)
Interferon Regulatory Factor-1/metabolism , Interferon Regulatory Factors/metabolism , Interferon-gamma/toxicity , Oligodendroglia/drug effects , Stem Cells/drug effects , Animals , Cell Death/drug effects , Cells, Cultured , Gene Expression/drug effects , Genes, Reporter , Humans , Interferon Regulatory Factor-1/genetics , Interferon Regulatory Factors/genetics , Interferon-beta/toxicity , Membrane Potential, Mitochondrial/drug effects , Oligodendroglia/cytology , Oligodendroglia/physiology , RNA, Small Interfering/genetics , RNA, Small Interfering/metabolism , Rats , Stem Cells/cytology , Stem Cells/physiology
12.
Rinsho Shinkeigaku ; 51(11): 1036-9, 2011 Nov.
Article in Japanese | MEDLINE | ID: mdl-22277471

ABSTRACT

Although neurological sequelae are attributable to poor regeneration of the central nervous system, oligodendrocytes demonstrate robust regenerative response even in adults. Accumulating evidence indicates that the glial cells identified by surface expression of the proteoglycan NG2 are the cellular source of newly-developed oligodendrocytes following demyelination, and thereby considered adult oligodendroglial progenitor cells (OPCs). Despite their robust regenerative capability, remyelination often ends up in failure or is incomplete, particularly after recurrent neuroinflammation, which is referred to as "remyelination failure". While axonal degeneration may contribute to remyelination failure, OPCs are also affected by neuroinflammation. Indeed, various studies have indicated that gamma-interferon, a proinflammatory cytokine associated with autoimmunity, is cytotoxic to OPCs by inducing cell death, and inhibiting their proliferation and differentiation. In contrast to gamma-interferon, we confirmed that beta-interferon which is used for the treatment of relapsing-remitting multiple sclerosis does not induce OPC death. Through a comprehensive analysis of gamma-interferon-inducible and beta-interferon-inducible genes in OPCs, we have identified interferon regulatory factor-1 and -8 (IRF1 and IRF8) as candidate transcription factors responsible for gamma-interferon-mediated cytotoxicity in OPCs. Validating and elaborating on these findings particularly in in vivo models may prove of importance in understanding remyelination failure and suggest therapeutic approaches to enhance remyelination.


Subject(s)
Demyelinating Diseases/physiopathology , Oligodendroglia/physiology , Animals , Cattle , Cell Death , Interferon-gamma/physiology , Mice
13.
Mitochondrion ; 10(2): 143-50, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20005986

ABSTRACT

Demyelination occurs in multiple inherited mitochondrial diseases. We studied which genes were induced as a consequence of differentiation in rodent and human oligodendroglia. Cholesterol, myelin and mitochondrial genes were significantly increased with oligodendroglial differentiation. Mitochondrial DNA content per cell and acetyl CoA-related transcripts increased significantly; thus, the large buildup of cholesterol necessary for myelination appears to require mitochondrial production of acetyl-CoA. Oligodendroglia were treated with low doses of the mitochondrial inhibitor rotenone to test the dependence of differentiation on mitochondrial function. Undifferentiated cells were resistant to rotenone, whereas differentiating cells were much more sensitive. Very low doses of rotenone that did not affect viability or ATP synthesis still inhibited differentiation, as measured by reduced levels of the myelin transcripts 2',3'-Cyclic Nucleotide-3'-Phosphodiesterase and Myelin Basic Protein. Thus, mitochondrial transcripts and mtDNA are amplified during oligodendroglial differentiation, and differentiating oligodendroglia are especially sensitive to mitochondrial inhibition, suggesting mechanisms for demyelination observed in mitochondrial disease.


Subject(s)
Cell Differentiation , Genes, Mitochondrial , Mitochondria/physiology , Oligodendroglia/physiology , Transcriptional Activation , Acetyl Coenzyme A/metabolism , Humans , Metabolic Networks and Pathways/genetics , Rotenone/pharmacology , Uncoupling Agents/pharmacology
14.
J Neuroimmunol ; 212(1-2): 53-64, 2009 Jul 25.
Article in English | MEDLINE | ID: mdl-19467717

ABSTRACT

Interferon-gamma induces major histocompatibility complex class II (MHC-II) in proliferating oligodendroglial progenitor cells (OPC), but to a much lesser extent in mature oligodendrocytes. Interferon-beta has virtually no effects on MHC-II induction even in OPC. Interferon-gamma-mediated transcriptional induction of CIITA, a critical regulator of MHC-II induction, was 6-fold lower in mature oligodendrocytes than in OPC, and entirely dependent on promoter IV, suggesting that the transcriptional activity of promoter IV is down-regulated after differentiation. The distinct difference in MHC-II induction between interferon-gamma and interferon-beta is attributed to transient interferon-beta-mediated activation of STAT1-IRF1 signaling compared to the sustained interferon-gamma-mediated activation.


Subject(s)
Cell Lineage , Genes, MHC Class II , Interferons/pharmacology , Oligodendroglia/immunology , Stem Cells/immunology , Animals , B7-1 Antigen/genetics , Cells, Cultured , DNA Methylation , Interferon Regulatory Factor-1/genetics , Interferon Regulatory Factor-1/physiology , Mice , Mice, Inbred C57BL , Nuclear Proteins/genetics , Trans-Activators/genetics , Transcription, Genetic/drug effects
15.
Biochem Biophys Res Commun ; 383(2): 258-62, 2009 May 29.
Article in English | MEDLINE | ID: mdl-19358824

ABSTRACT

Rapid and persistent activation of c-JUN is necessary for axonal regeneration after nerve injury, although upstream molecular events leading to c-JUN activation remain largely unknown. ZPK/DLK/MAP3K12 activates the c-Jun N-terminal kinase pathway at an apical level. We investigated axonal regeneration of the dorsal root ganglion (DRG) neurons of homozygous ZPK/DLK gene-trap mice. In vitro neurite extension assays using DRG explants from 14day-old mice revealed that neurite growth rates of the ZPK/DLK gene-trap DRG explants were reduced compared to those of the wild-type DRG explants. Three ZPK/DLK gene-trap mice which survived into adulthood were subjected to sciatic nerve axotomy. At 24h after axotomy, phosphorylated c-JUN-positive DRG neurons were significantly less frequent in ZPK/DLK gene-trap mice than in wild-type mice. These results indicate that ZPK/DLK is involved in regenerative responses of mammalian DRG neurons to axonal injury through activation of c-JUN.


Subject(s)
Axons/physiology , Ganglia, Spinal/injuries , MAP Kinase Kinase Kinases/physiology , Nerve Regeneration , Sensory Receptor Cells/physiology , Animals , Axons/enzymology , Cell Line , Enzyme Activation , Ganglia, Spinal/cytology , Ganglia, Spinal/physiology , JNK Mitogen-Activated Protein Kinases/metabolism , MAP Kinase Kinase Kinases/genetics , Mice , Molecular Sequence Data , Nerve Regeneration/genetics , Sensory Receptor Cells/enzymology
16.
Eur J Neurosci ; 30(11): 2030-41, 2009 Dec 03.
Article in English | MEDLINE | ID: mdl-20128842

ABSTRACT

Highly purified oligodendroglial lineage cells from mice lacking functional bax and bak genes were resistant to apoptosis after in-vitro differentiation, indicating an essential role of the intrinsic apoptotic pathway in apoptosis of oligodendrocytes in the absence of neurons (axons) and other glial cells. These mice therefore provide a valuable tool with which to evaluate the significance of the intrinsic apoptotic pathway in regulating the population sizes of oligodendrocytes and oligodendroglial progenitor cells. Quantitative analysis of the optic nerves and the dorsal columns of the spinal cord revealed that the absolute numbers of mature oligodendrocytes immunolabeled for aspartoacylase and adult glial progenitor cells expressing NG2 chondroitin sulfate proteoglycan were increased in both white matter tracts of adult bax/bak-deficient mice and, to a lesser extent, bax-deficient mice, except that there was no increase in NG2-positive progenitor cells in the dorsal columns of these strains of mutant mice. These increases in mature oligodendrocytes and progenitor cells in bax/bak-deficient mice were unexpectedly proportional to increases in numbers of axons in these white matter tracts, thus retaining the oligodendroglial lineage to axon ratios of at most 1.3-fold of the physiological numbers. This is in contrast to the prominent expansion in numbers of neural precursor cells in the subventricular zones of these adult mutant mice. Our study indicates that homeostatic control of cell number is different for progenitors of the oligodendroglial and neuronal lineages. Furthermore, regulatory mechanism(s) operating in addition to apoptotic elimination through the intrinsic pathway, appear to prevent the overproduction of highly mitotic oligodendroglial progenitor cells.


Subject(s)
Axons/physiology , Oligodendroglia/physiology , bcl-2 Homologous Antagonist-Killer Protein/deficiency , bcl-2-Associated X Protein/deficiency , Animals , Animals, Newborn , Antigens/metabolism , Apoptosis/genetics , Brain/cytology , Cell Death/genetics , Cell Differentiation/genetics , Cells, Cultured , Gangliosides/metabolism , Gene Expression Regulation/genetics , In Situ Nick-End Labeling/methods , Mice , Mice, Knockout , Myelin Basic Protein/metabolism , Myelin Sheath/metabolism , O Antigens/metabolism , Optic Nerve/cytology , Optic Nerve/growth & development , Optic Nerve/metabolism , Proteoglycans/metabolism , Proto-Oncogene Proteins c-bcl-6/genetics , Proto-Oncogene Proteins c-bcl-6/metabolism , RNA, Messenger/metabolism , Stem Cells/physiology , Time Factors , bcl-2 Homologous Antagonist-Killer Protein/genetics , bcl-2-Associated X Protein/genetics
17.
Glia ; 56(11): 1238-49, 2008 Aug 15.
Article in English | MEDLINE | ID: mdl-18452213

ABSTRACT

Acid-sensing ion channels (ASICs) are widely expressed in neurons, where they serve in pain and mechanical sensation, and contribute to learning and memory. Six ASIC subunit proteins form homo- or heteromeric channel complexes with distinct physiological properties. Of such complexes, only monomeric ASIC1a channels are Ca2+ permeable. Prior pharmacologic and genetic studies have shown that ASIC1a channel inactivation markedly diminishes CNS susceptibility to ischemic damage. Here, we characterize ASIC expression in oligodendrocyte lineage cells (OLC) by molecular, electrophysiological, calcium imaging, and immunofluorescence techniques. ASIC1a, ASIC2a, and ASIC4 mRNAs were expressed in cultured rat OLC, with steady-state levels of each of these mRNAs several-fold higher in oligodendroglial progenitors than in mature oligodendroglia. ASIC transcripts were also detected in brain white matter, and ASIC1a protein expression was detected in white matter oligodendroglia. Inactivating, proton-gated, amiloride-sensitive OLC currents were detected by whole-cell voltage clamp. These currents showed profound tachyphylaxis with slow recovery, and were predominantly blocked by psalmotoxin, indicating that homomeric ASIC1a comprised a large fraction of functional ASIC in the cultured OLC. ASIC activation substantially depolarized OLC plasma membrane in current clamp studies, and elicited transient elevations in intracellular Ca2+ in imaging studies. Thus, OLC ASIC1a channels provide a means by which an acid shift in CNS extracellular pH, by diminishing plasma membrane potential and increasing Ca2+ permeability, can activate OLC signaling pathways, and may contribute to OLC vulnerability to CNS ischemia.


Subject(s)
Cell Lineage/physiology , Gene Expression Regulation, Developmental/physiology , Nerve Tissue Proteins/biosynthesis , Oligodendroglia/metabolism , Sodium Channels/biosynthesis , Acid Sensing Ion Channels , Animals , Animals, Newborn , Cells, Cultured , Central Nervous System/chemistry , Central Nervous System/metabolism , Central Nervous System/physiology , Mice , Mice, Inbred C57BL , Mice, Transgenic , Nerve Tissue Proteins/genetics , Oligodendroglia/cytology , Rats , Rats, Sprague-Dawley , Sodium Channels/genetics , Stem Cells/cytology , Stem Cells/metabolism
18.
J Neurochem ; 102(4): 1064-70, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17472701

ABSTRACT

We adopted a genetic approach to test the importance of edited GluR2-free, Ca(2+)-permeable, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptors in the pathophysiology of experimental autoimmune encephalomyelitis, an inflammatory demyelinative disorder resembling multiple sclerosis. Initial studies showed that oligodendroglial lineage cells from mice lacking functional copies of the gene encoding the GluR3 AMPA receptor subunit (Gria3) had a diminished capacity to assemble edited GluR2-free AMPA receptors, and were resistant to excitotoxicity in vitro. Neurological deficits and spinal cord demyelination elicited by immunization with myelin oligodendrocyte glycoprotein peptide were substantially milder in these Gria3 mutant mice than in their wild-type littermates. These results support the hypothesis that oligodendroglial excitotoxicity mediated by AMPA receptors that do not contain edited GluR2 subunits contributes to demyelination in experimental autoimmune encephalomyelitis, and suggest that inhibiting these Ca(2+)-permeable AMPA receptors would be therapeutic in multiple sclerosis.


Subject(s)
Demyelinating Diseases/genetics , Encephalomyelitis, Autoimmune, Experimental/genetics , Encephalomyelitis, Autoimmune, Experimental/physiopathology , Receptors, AMPA/deficiency , Animals , Animals, Newborn , Brain/cytology , Brain/metabolism , Brain/pathology , Cells, Cultured , Demyelinating Diseases/pathology , Encephalomyelitis, Autoimmune, Experimental/pathology , Excitatory Amino Acid Agents/pharmacology , Female , Gene Expression Regulation/genetics , Kainic Acid/pharmacology , Membrane Potentials/drug effects , Membrane Potentials/physiology , Mice , Mice, Knockout , Neuroglia/physiology , Patch-Clamp Techniques/methods , RNA, Messenger/biosynthesis , Receptors, AMPA/metabolism , Receptors, Glutamate/genetics , Receptors, Glutamate/metabolism , Reverse Transcriptase Polymerase Chain Reaction/methods , Spermine/analogs & derivatives , Spermine/pharmacology , Statistics, Nonparametric
19.
J Biol Chem ; 281(29): 20095-106, 2006 Jul 21.
Article in English | MEDLINE | ID: mdl-16728393

ABSTRACT

Oligodendrocytes are exposed to various cytokines in inflammatory lesions in the central nervous system. In this study, we focused on the direct effects of interferon-gamma (IFNG) on highly purified rat oligodendroglial cultures at different developmental stages. Among the three stages tested, IFNG had direct cytotoxic effects on actively proliferating oligodendrocyte progenitors but much less on immature oligodendrocytes and none on mature oligodendrocytes. This stage-specific susceptibility of progenitors to IFNG-induced cytotoxicity consisted of two components, delay in the G(1)/S transition of the cell cycle and increased cell death at least partly mediated by apoptosis, suggesting that progression of the cell cycle was tightly linked to this toxic mechanism. There was no functional difference in the signal transducers and activators of transcription (STAT) pathways between progenitors and mature oligodendrocytes as determined by induction of IRF1 mRNA in response to IFNG. We found that partial inhibition of the MEK-ERK pathway, one of the mitogen-activated protein kinase phosphorelay modules, by U0126 partially reversed the IFNG-induced cytotoxicity in progenitors. In addition, ERK activity was quickly down-regulated after in vitro differentiation of progenitors to immature oligodendrocytes. Therefore, we concluded that simultaneous activation of the STAT pathway by IFNG and of the ERK pathway by exogenous trophic factors played a role in the stage-specific IFNG-induced cytotoxicity in oligodendroglial progenitors. Our study has implications with respect to the mechanisms of periventricular leukomalacia in infants and of persistent demyelination in multiple sclerosis lesions in adults.


Subject(s)
Cell Death , Extracellular Signal-Regulated MAP Kinases/metabolism , Interferon-gamma/pharmacology , MAP Kinase Kinase Kinases/metabolism , Oligodendroglia/cytology , Adult , Animals , Base Sequence , Cell Death/drug effects , Cell Survival/drug effects , Cells, Cultured , Culture Media , DNA Primers , Demyelinating Diseases/pathology , Humans , Kainic Acid/pharmacology , Molecular Sequence Data , Oligodendroglia/drug effects , Oligodendroglia/physiology , Rats , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction , Stem Cells/cytology , Stem Cells/drug effects , Stem Cells/physiology
20.
J Agric Food Chem ; 53(15): 6112-6, 2005 Jul 27.
Article in English | MEDLINE | ID: mdl-16029004

ABSTRACT

Morphiceptin (Tyr-Pro-Phe-Pro-NH(2)), tetrapeptide, was synthesized using dipeptidyl aminopeptidase IV (DP IV, EC 3.4.14.5) derived from Aspergillus oryzae RIB 915 as a catalyst. Tyr-Pro-OEt was incubated with Phe-Pro-NH(2) in the presence of DP IV under various conditions of temperature, concentrations of ethylene glycol, pH, reaction time, and others. Morphiceptin was obtained at 40% yield under the optimal reaction conditions: substrate, 4 mM Tyr-Pro-OEt.HCl and 20 mM Phe-Pro-NH(2).HCl; enzyme, DP IV, 0.275 nkat; solvent, 60% ethylene glycol containing 20 mM phosphate buffer at pH 7.0; amine, 4.2 mM diisopropylamine at 4 degrees C for 24 h. Amino group protection was unnecessary for synthesis of morphiceptin by DP IV.


Subject(s)
Aspergillus oryzae/enzymology , Dipeptidyl-Peptidases and Tripeptidyl-Peptidases/metabolism , Endorphins/biosynthesis , Ethylene Glycol , Hydrogen-Ion Concentration
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