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1.
Neurobiol Dis ; 186: 106263, 2023 10 01.
Article in English | MEDLINE | ID: mdl-37591465

ABSTRACT

The R47H variant of triggering receptor expressed on myeloid cells 2 (TREM2) increases the risk of Alzheimer's disease (AD). To investigate potential mechanisms, we analyzed knockin mice expressing human TREM2-R47H from one mutant mouse Trem2 allele. TREM2-R47H mice showed increased seizure activity in response to an acute excitotoxin challenge, compared to wildtype controls or knockin mice expressing the common variant of human TREM2. TREM2-R47H also increased spontaneous thalamocortical epileptiform activity in App knockin mice expressing amyloid precursor proteins bearing autosomal dominant AD mutations and a humanized amyloid-ß sequence. In mice with or without such App modifications, TREM2-R47H increased the density of putative synapses in cortical regions without amyloid plaques. TREM2-R47H did not affect synaptic density in hippocampal regions with or without plaques. We conclude that TREM2-R47H increases AD-related network hyperexcitability and that it may do so, at least in part, by causing an imbalance in synaptic densities across brain regions.


Subject(s)
Alzheimer Disease , Humans , Animals , Mice , Alzheimer Disease/genetics , Alleles , Seizures , Amyloid beta-Peptides , Disease Models, Animal , Plaque, Amyloid , Synapses , Membrane Glycoproteins/genetics , Receptors, Immunologic/genetics
2.
Elife ; 102021 04 12.
Article in English | MEDLINE | ID: mdl-33843585

ABSTRACT

Visual perception in natural environments depends on the ability to focus on salient stimuli while ignoring distractions. This kind of selective visual attention is associated with gamma activity in the visual cortex. While the nucleus reticularis thalami (nRT) has been implicated in selective attention, its role in modulating gamma activity in the visual cortex remains unknown. Here, we show that somatostatin- (SST) but not parvalbumin-expressing (PV) neurons in the visual sector of the nRT preferentially project to the dorsal lateral geniculate nucleus (dLGN), and modulate visual information transmission and gamma activity in primary visual cortex (V1). These findings pinpoint the SST neurons in nRT as powerful modulators of the visual information encoding accuracy in V1 and represent a novel circuit through which the nRT can influence representation of visual information.


Subject(s)
Gamma Rhythm/physiology , Neurons/physiology , Thalamic Nuclei/physiology , Visual Cortex/physiology , Visual Perception/physiology , Animals , Female , Male , Mice , Somatostatin/metabolism
3.
Nat Commun ; 10(1): 4344, 2019 09 25.
Article in English | MEDLINE | ID: mdl-31554802

ABSTRACT

Innate immune responses to Zika virus (ZIKV) are dampened in the lower female reproductive tract (LFRT) compared to other tissues, but the mechanism that underlies this vulnerability is poorly understood. Using tissues from uninfected and vaginally ZIKV-infected macaques and mice, we show that low basal expression of RNA-sensing pattern recognition receptors (PRRs), or their co-receptors, in the LFRT contributes to high viral replication in this tissue. In the LFRT, ZIKV sensing provides limited protection against viral replication, and the sensors are also minimally induced after vaginal infection. While IFNα/ß receptor signaling offers minimal protection in the LFRT, it is required to prevent dissemination of ZIKV to other tissues, including the upper FRT. Our findings support a role for RNA-sensing PRRs in the dampened innate immunity against ZIKV in the LFRT compared to other tissues and underlie potential implications for systemic dissemination upon heterosexual transmission of ZIKV in women.


Subject(s)
Genitalia, Female/immunology , Immunity, Innate/immunology , RNA, Viral/immunology , Zika Virus Infection/immunology , Zika Virus/immunology , Animals , Female , Gene Expression Regulation, Viral , Genitalia, Female/metabolism , Genitalia, Female/virology , Humans , Immunity, Innate/genetics , Macaca mulatta , Mice, Inbred C57BL , Mice, Knockout , RNA, Viral/genetics , Receptor, Interferon alpha-beta/genetics , Receptor, Interferon alpha-beta/immunology , Receptor, Interferon alpha-beta/metabolism , Receptors, Pattern Recognition/genetics , Receptors, Pattern Recognition/immunology , Receptors, Pattern Recognition/metabolism , Toll-Like Receptor 3/genetics , Toll-Like Receptor 3/immunology , Toll-Like Receptor 3/metabolism , Vagina/immunology , Vagina/metabolism , Vagina/virology , Virus Replication/genetics , Virus Replication/immunology , Zika Virus/genetics , Zika Virus/physiology , Zika Virus Infection/genetics , Zika Virus Infection/virology
4.
J Clin Invest ; 126(8): 2855-66, 2016 08 01.
Article in English | MEDLINE | ID: mdl-27400128

ABSTRACT

Hypertriglyceridemia is an independent risk factor for cardiovascular disease, and plasma triglycerides (TGs) correlate strongly with plasma apolipoprotein C-III (ApoC-III) levels. Antisense oligonucleotides (ASOs) for ApoC-III reduce plasma TGs in primates and mice, but the underlying mechanism of action remains controversial. We determined that a murine-specific ApoC-III-targeting ASO reduces fasting TG levels through a mechanism that is dependent on low-density lipoprotein receptors (LDLRs) and LDLR-related protein 1 (LRP1). ApoC-III ASO treatment lowered plasma TGs in mice lacking lipoprotein lipase (LPL), hepatic heparan sulfate proteoglycan (HSPG) receptors, LDLR, or LRP1 and in animals with combined deletion of the genes encoding HSPG receptors and LDLRs or LRP1. However, the ApoC-III ASO did not lower TG levels in mice lacking both LDLR and LRP1. LDLR and LRP1 were also required for ApoC-III ASO-induced reduction of plasma TGs in mice fed a high-fat diet, in postprandial clearance studies, and when ApoC-III-rich or ApoC-III-depleted lipoproteins were injected into mice. ASO reduction of ApoC-III had no effect on VLDL secretion, heparin-induced TG reduction, or uptake of lipids into heart and skeletal muscle. Our data indicate that ApoC-III inhibits turnover of TG-rich lipoproteins primarily through a hepatic clearance mechanism mediated by the LDLR/LRP1 axis.


Subject(s)
Apolipoprotein C-III/blood , Lipoproteins/blood , Low Density Lipoprotein Receptor-Related Protein-1/metabolism , Receptors, LDL/metabolism , Triglycerides/blood , Tumor Suppressor Proteins/metabolism , Animals , Female , Genotype , Heparin/pharmacology , Hepatocytes/metabolism , Ketones/metabolism , Liver/metabolism , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Myocardium/metabolism , Risk Factors
5.
J Nurs Educ ; 44(12): 533-40, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16402735

ABSTRACT

The shortage of nurses in Kuwait is attributed to low production of indigenous nurses, resignation and emigration of foreign nurses, and expansion of health care facilities. This study explored Kuwaiti high school students' perceptions of nursing as a profession, their sources of information about nursing, and factors that affected their choice of nursing as a future career. Questionnaires from 289 students attending seven all-female high schools in Kuwait were analyzed. The results revealed that all of the participants were knowledgeable about the functional aspects of the nursing profession, and 35% of them received this information through contact with nurses during hospital visits. However, only 19% indicated they might consider nursing as a future career. The implications of the study for nursing education and practice, and strategies to attract and retain indigenous high school graduates into nursing programs in Kuwait are discussed.


Subject(s)
Attitude to Health , Career Choice , Nursing/organization & administration , Students/psychology , Adolescent , Adult , Education, Nursing, Associate , Education, Nursing, Baccalaureate , Female , Health Services Needs and Demand , Humans , Kuwait , Mass Media , Nurse's Role , Nursing Staff/organization & administration , Peer Group , Personnel Selection , Power, Psychological , Professional Autonomy , Salaries and Fringe Benefits , Social Perception , Stereotyping , Surveys and Questionnaires , Training Support
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