Cerebrospinal fluid levels of MMP-2, 7, and 9 are elevated in association with human immunodeficiency virus dementia.

Abstract:

:Pathological evidence suggests that alterations of the blood-brain barrier (BBB) may occur in association with human immunodeficiency virus (HIV) dementia (HIVD). Increased BBB permeability could contribute to the development of dementia by facilitating the entry of activated and infected monocytes, as well as potentially toxic serum proteins, into the central nervous system. One mechanism by which BBB permeability may be altered is through increased activity of select matrix metalloproteinases (MMPs). In the present study, we examined the possibility that MMPs that target critical BBB proteins, including laminin, entactin, and collagen type IV, are elevated in the cerebrospinal fluid (CSF) of patients with HIVD. We also examined the possibility that such MMPs could be produced by brain-derived cells, and that MMP production by these cells might be increased by tumor necrosis factor-alpha, an inflammatory cytokine that is produced by HIV-infected monocytes/microglia and is elevated in HIVD. By using western blot and enzyme-linked immunosorbent assay, we observed that CSF levels of pro-MMP-2 and pro-MMP-7 were increased in association with HIVD. In addition, through the use of gelatin substrate zymography, a sensitive functional assay for MMP-2 and MMP-9, we observed that MMP-2 or pro-MMP-9 activity was more frequently detectable in the CSF of individuals with HIV dementia (9/16) than in the CSF from either nondemented seropositive (2/11) or seronegative (0/11) controls. Although the presence of MMPs in the serum could contribute to elevated levels in the CSF, we also show that brain-derived cells release MMP-2, 7, and 9, and that such release is increased after their stimulation with tumor necrosis factor-alpha. Together, these results suggest that elevated CSF levels of select MMPs may reflect immune activation within the central nervous system. They also suggest that further studies may be warranted to determine whether these proteins may play a role in the development of symptomatic neurological disease.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Conant K,McArthur JC,Griffin DE,Sjulson L,Wahl LM,Irani DN

doi

10.1002/1531-8249(199909)46:3<391::aid-ana15>3.0.c

keywords:

subject

Has Abstract

pub_date

1999-09-01 00:00:00

pages

391-8

issue

3

eissn

0364-5134

issn

1531-8249

journal_volume

46

pub_type

杂志文章
  • A surface-in gradient of thalamic damage evolves in pediatric multiple sclerosis.

    abstract:OBJECTIVE:Central nervous system pathology in multiple sclerosis includes both focal inflammatory perivascular injury and injury to superficial structures, including the subpial region of the cortex, which reportedly exhibits a gradient of damage from the surface inward. We assessed how early in the multiple sclerosis ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25429

    authors: Fadda G,Brown RA,Magliozzi R,Aubert-Broche B,O'Mahony J,Shinohara RT,Banwell B,Marrie RA,Yeh EA,Collins DL,Arnold DL,Bar-Or A,Canadian Pediatric Demyelinating Disease Network.

    更新日期:2019-03-01 00:00:00

  • Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3).

    abstract:OBJECTIVE:Nemaline myopathy (NM) is one of the most common congenital nondystrophic myopathies and is characterized by muscle weakness, often from birth. Mutations in ACTA1 are a frequent cause of NM (ie, NEM3). ACTA1 encodes alpha-actin 1, the main constituent of the sarcomeric thin filament. The mechanisms by which m...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25144

    authors: Joureau B,de Winter JM,Conijn S,Bogaards SJP,Kovacevic I,Kalganov A,Persson M,Lindqvist J,Stienen GJM,Irving TC,Ma W,Yuen M,Clarke NF,Rassier DE,Malfatti E,Romero NB,Beggs AH,Ottenheijm CAC

    更新日期:2018-02-01 00:00:00

  • Neurophysiological techniques as an aid to surgical treatment of primary brain tumors.

    abstract::We describe a method of cortical stimulation for localizing functional areas of brain before operation for primary brain tumors that was carried out in 14 patients. The method is unique in that the stimulation is done over several days using chronically indwelling subdural electrode arrays. In addition to cortical sti...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410190607

    authors: Morris HH 3rd,Lüders H,Hahn JF,Lesser RP,Dinner DS,Estes ML

    更新日期:1986-06-01 00:00:00

  • Cerebral hemorrhage produced by ruptured dissecting aneurysm in miliary aneurysm.

    abstract::This report describes, for what may be only the second time, a ruptured miliary aneurysm within a cerebral hemorrhage. The report is unique in that the aneurysm has arisen at the site of a dissection within the wall of an arteriole at a site of fibrinoid necrosis. The case not only is a unique illustration of this pat...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10664

    authors: Rosenblum WI

    更新日期:2003-09-01 00:00:00

  • Proteasome inhibitor-induced model of Parkinson's disease.

    abstract::We recently reported that systemic administration of a proteasome inhibitor induced a progressive levodopa-responsive, bradykinetic syndrome in rats with imaging, pathological, and biochemical features that strikingly resemble what is found in PD. This model has the potential to be a useful tool for studying the mecha...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20936

    authors: McNaught KS,Olanow CW

    更新日期:2006-08-01 00:00:00

  • Alzheimer neurofibrillary tangles: antiserum and immunohistological staining.

    abstract::A 50,000-dalton polypeptide has been purified from fractions enriched with neurofibrillary tangles of paired helical filaments from human autopsy specimens of Alzheimer disease and senile dementia of the Alzheimer type. An antiserum to this polypeptide was raised in a rabbit. This antiserum formed an immunoprecipitati...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410060612

    authors: Grundke-Iqbal I,Johnson AB,Terry RD,Wisniewski HM,Iqbal K

    更新日期:1979-12-01 00:00:00

  • Extended levodopa release from a subcutaneously implanted polymer matrix in rats.

    abstract::It is well recognized that plasma fluctuations resulting from oral levodopa therapy may cause an unstable clinical response in parkinsonian patients. We have therefore developed a slow-release polymer matrix system that can deliver levodopa continuously for extended periods of time (at least 225 days) after subcutaneo...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410280519

    authors: Sabel BA,Dominiak P,Hüaser W,During MJ,Freese A

    更新日期:1990-11-01 00:00:00

  • Augmented anti-acetylcholine receptor response following long-term penicillamine administration.

    abstract::Because of the association of D-penicillamine (DP) therapy with myasthenia gravis, we have studied long-term DP treatment in five inbred strains of mice with doses comparable to those used in patients with rheumatoid arthritis. No clinical weakness or anti-acetylcholine receptor (AChR) antibody developed with up to 6 ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410160103

    authors: Bever CT Jr,Dretchen KL,Blake GJ,Chang HW,Penn AS,Asofsky R

    更新日期:1984-07-01 00:00:00

  • Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.

    abstract::Genomic triplication of the alpha-synuclein gene recently has been associated with familial Parkinson's disease in the Spellman-Muenter kindred. Here, we present an independent family, of Swedish-American descent, with hereditary early-onset parkinsonism with dementia due to alpha-synuclein triplication. Brain tissue ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10846

    authors: Farrer M,Kachergus J,Forno L,Lincoln S,Wang DS,Hulihan M,Maraganore D,Gwinn-Hardy K,Wszolek Z,Dickson D,Langston JW

    更新日期:2004-02-01 00:00:00

  • Lymph nodes--a possible site for sympathetic neuronal regulation of immune responses.

    abstract::Noradrenergic fibers were identified in rat cervical lymph nodes by fluorescence histochemistry and confirmed by radioenzymatic determination of norepinephrine. After superior cervical ganglionectomy, lymph node norepinephrine and noradrenergic fluorescence were strikingly decreased. The alpha-adrenergic radioligand [...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410080509

    authors: Giron LT Jr,Crutcher KA,Davis JN

    更新日期:1980-11-01 00:00:00

  • Interneuron activity leads to initiation of low-voltage fast-onset seizures.

    abstract::Seizures in temporal lobe epilepsy can be classified as hypersynchronous and low-voltage fast according to their onset patterns. Experimental evidence suggests that low-voltage fast-onset seizures mainly result from the synchronous activity of γ-aminobutyric acid-releasing cells. In this study, we tested this hypothes...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24342

    authors: Shiri Z,Manseau F,Lévesque M,Williams S,Avoli M

    更新日期:2015-03-01 00:00:00

  • Benzodiazepine receptors and diazepam-binding inhibitor in human cerebral tumors.

    abstract::Benzodiazepines can regulate neoplastic growth and immune response through specific peripheral benzodiazepine receptors. We investigated the presence of peripheral and classic central benzodiazepine receptors as well as diazepam-binding inhibitor, an endogenous ligand of both types of receptors, in different human cer...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410260411

    authors: Ferrarese C,Appollonio I,Frigo M,Gaini SM,Piolti R,Frattola L

    更新日期:1989-10-01 00:00:00

  • Cerebrospinal fluid polyamines: biochemical markers of malignant childhood brain tumors.

    abstract::The clinical value of cerebrospinal fluid (CSF) polyamine determinations in childhood medulloblastoma has been suggested. We performed 72 CSF polyamine determinations in 35 children with primary brain tumors. Spermine values were normal and spermidine values were inconsistently elevated. CSF putrescine values, however...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410190409

    authors: Phillips PC,Kremzner LT,De Vivo DC

    更新日期:1986-04-01 00:00:00

  • Disturbance of oxidative metabolism of glucose in recent human cerebral infarcts.

    abstract::Eight patients with recent cerebral hemispheric infarction were studied with positron emission tomography and the oxygen-15 steady-state inhalation and [18F]deoxyglucose techniques to obtain values of regional cerebral blood flow, oxygen consumption, and glucose metabolism. The Sokoloff equation, used to calculate glu...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410140605

    authors: Wise RJ,Rhodes CG,Gibbs JM,Hatazawa J,Palmer T,Frackowiak RS,Jones T

    更新日期:1983-12-01 00:00:00

  • A channelopathy contributes to cerebellar dysfunction in a model of multiple sclerosis.

    abstract:OBJECTIVE:Cerebellar dysfunction in multiple sclerosis (MS) contributes significantly to disability, is relatively refractory to symptomatic therapy, and often progresses despite treatment with disease-modifying agents. We previously observed that sodium channel Nav1.8, whose expression is normally restricted to the pe...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.22665

    authors: Shields SD,Cheng X,Gasser A,Saab CY,Tyrrell L,Eastman EM,Iwata M,Zwinger PJ,Black JA,Dib-Hajj SD,Waxman SG

    更新日期:2012-02-01 00:00:00

  • Absence of REM and altered NREM sleep in patients with spinocerebellar degeneration and slow saccades.

    abstract::The pontine tegmentum contains the neurons responsible for generation of saccadic eye movements and certain phases of sleep. We studied two genetically unrelated patients with spinocerebellar degeneration and slow saccadic eye movements. Multiple all-night sleep studies in both patients disclosed absence of REM and st...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410070312

    authors: Osorio I,Daroff RB

    更新日期:1980-03-01 00:00:00

  • Cerebral hemodynamics and metabolism in pseudotumor cerebri.

    abstract::A comprehensive analysis of cerebral hemodynamics and metabolism was carried out in 14 patients with pseudotumor cerebri. Tracer techniques were employed to measure cerebral blood flow (CBF) and vascular reactivity to acute changes in arterial carbon dioxide tension and blood pressure, cerebral blood volume (CBV), and...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410040203

    authors: Raichle ME,Grubb RL Jr,Phelps ME,Gado MH,Caronna JJ

    更新日期:1978-08-01 00:00:00

  • Approach to the diagnosis of neurotransmitter diseases exemplified by the differential diagnosis of childhood-onset dystonia.

    abstract::We present our approach to the diagnosis of pediatric neurotransmitter diseases exemplified by the differential diagnosis of children presenting with dystonia. This approach is based upon the primary aim of early diagnosis of treatable conditions and the need for a logical series of investigations. We have tried to be...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.10628

    authors: Assmann B,Surtees R,Hoffmann GF

    更新日期:2003-01-01 00:00:00

  • Motor outcome prediction using diffusion tensor tractography in pontine infarct.

    abstract::We investigated whether the integrity of the corticospinal tract classified by diffusion tensor tractography (DTT) can predict the motor outcome in 25 patients with pontine infarct. DTTs were obtained in the early stage of stroke (5-30 days) and were classified into two groups (type A: the integrity of corticospinal t...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.21444

    authors: Jang SH,Bai D,Son SM,Lee J,Kim DS,Sakong J,Kim DG,Yang DS

    更新日期:2008-10-01 00:00:00

  • Absence of N-acetylaspartate in the human brain: impact on neurospectroscopy?

    abstract::N-acetylaspartate (NAA) contributes to the most prominent signal in proton magnetic resonance spectroscopy (1H-MRS) of the adult human brain. We report the absence of NAA in the brain of a 3-year-old child with neurodevelopmental retardation and moderately delayed myelination. Since normal concentration of NAA in body...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Martin E,Capone A,Schneider J,Hennig J,Thiel T

    更新日期:2001-04-01 00:00:00

  • Defining neurodegeneration on Guam by targeted genomic sequencing.

    abstract:OBJECTIVE:Amyotrophic lateral sclerosis/parkinsonism-dementia complex has been described in Guam, Western Papua, and the Kii Peninsula of Japan. The etiology and pathogenesis of this complex neurodegenerative disease remains enigmatic. METHODS:In this study, we have used targeted genomic sequencing to evaluate the con...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24346

    authors: Steele JC,Guella I,Szu-Tu C,Lin MK,Thompson C,Evans DM,Sherman HE,Vilariño-Güell C,Gwinn K,Morris H,Dickson DW,Farrer MJ

    更新日期:2015-03-01 00:00:00

  • Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p.

    abstract::We describe the clinical and oculographic findings in 4 families with episodic ataxia and interictal nystagmus (EA-2) linked to chromosome 19p. Episodes varied from pure ataxia to combinations of symptoms suggesting involvement of the cerebellum, brainstem, and cortex. Some affected individuals exhibited a progressive...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410410105

    authors: Baloh RW,Yue Q,Furman JM,Nelson SF

    更新日期:1997-01-01 00:00:00

  • Postmortem observations on beta-glucuronidase deficiency presenting as hydrops fetalis.

    abstract::This study reports a case of type VII mucopolysaccharidosis (beta-glucuronidase deficiency) presenting as lethal hydrops fetalis. Skin fibroblast cultures established postmortem revealed deficient beta-glucuronidase activity. Mucopolysaccharides were stored in various cells of the brain, heart, kidney, liver, and sple...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410140415

    authors: Irani D,Kim HS,El-Hibri H,Dutton RV,Beaudet A,Armstrong D

    更新日期:1983-10-01 00:00:00

  • Inborn errors of urea synthesis.

    abstract::Inborn errors of urea synthesis can present in the newborn period as a catastrophic illness or later in childhood or adulthood with an indolent course punctuated by hyperammonemic episodes. Because symptoms mimic other neuropsychiatric disorders, it is common for there to be a delay in diagnosis, often with dire conse...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410350204

    authors: Batshaw ML

    更新日期:1994-02-01 00:00:00

  • X-linked ataxia, weakness, deafness, and loss of vision in early childhood with a fatal course.

    abstract::An X-linked recessive disease with, in almost all patients, a fatal course in early childhood, occurring in a five-generation family is described. The 12 affected boys had early-onset floppiness, ataxia, liability to infections especially of the upper respiratory tract, deafness, and later, a flaccid tetraplegia and a...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410330519

    authors: Arts WF,Loonen MC,Sengers RC,Slooff JL

    更新日期:1993-05-01 00:00:00

  • An immunohistochemical study on alpha-ketoglutarate dehydrogenase complex in Parkinson's disease.

    abstract::We report an immunohistochemical study of the mitochondrial alpha-ketoglutarate dehydrogenase complex (KGDHC) in the substantia nigra in Parkinson's disease. The KGDHC, the three enzyme complex catalyzing the oxidation of alpha-ketoglutarate to succinate through succinic semialdehyde, is the rate-regulating enzyme of ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410350212

    authors: Mizuno Y,Matuda S,Yoshino H,Mori H,Hattori N,Ikebe S

    更新日期:1994-02-01 00:00:00

  • Central levodopa metabolism in Parkinson's disease after administration of stable isotope-labeled levodopa.

    abstract::We report the use of a new stable isotope-labeled form of levodopa (LD) to examine in vivo central LD metabolism in Parkinson's disease (PD). Eight patients representing a wide spectrum of disease severity were administered 50 mg of carbidopa orally followed in 1 hour by an intravenous bolus of 150 mg of stable isotop...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410420305

    authors: Durso R,Evans JE,Josephs E,Szabo GK,Evans BA,Handler JS,Jennings D,Browne TR

    更新日期:1997-09-01 00:00:00

  • Evidence for mitochondrial dysfunction in patients with alternating hemiplegia of childhood.

    abstract::Phosphorus magnetic resonance spectra of resting muscle were obtained from 4 patients with alternating hemiplegia of childhood. All patients had abnormally high resonance intensities from inorganic phosphate and an abnormally low calculated cytosolic phosphorylation potential. Two of the 4 patients had abnormally low ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410330608

    authors: Arnold DL,Silver K,Andermann F

    更新日期:1993-06-01 00:00:00

  • Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsy.

    abstract:OBJECTIVE:Autosomal-dominant lateral temporal epilepsy (ADLTE) is a genetic focal epilepsy characterized by auditory symptoms. Two genes, LGI1 and RELN, encoding secreted proteins, are implicated in the etiology of ADLTE, but half of the affected families remain genetically unsolved, and the underlying molecular mechan...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25167

    authors: Dazzo E,Rehberg K,Michelucci R,Passarelli D,Boniver C,Vianello Dri V,Striano P,Striano S,Pasterkamp RJ,Nobile C

    更新日期:2018-03-01 00:00:00

  • Hypoglycemia alters striatal amino acid efflux in perinatal rats: an in vivo microdialysis study.

    abstract::In adult brain, during insulin-induced hypoglycemia, striatal extracellular fluid concentrations of the excitatory amino acids glutamate and aspartate rise markedly (fourfold to tenfold). In this study, we used in vivo microdialysis to determine if insulin-induced hypoglycemia altered striatal amino acid efflux in sim...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410280408

    authors: Silverstein FS,Simpson J,Gordon KE

    更新日期:1990-10-01 00:00:00