Induction of DNA Methylation by Artificial piRNA Production in Male Germ Cells

SummaryGlobal DNA demethylation and subsequent de novo DNA methylation take place in mammalian male embryonic germ cells [1–3]. P-element-induced wimpy testis (PIWI)-interacting RNAs (piRNAs), which are germline-specific small RNAs, have been postulated to be critically important for de novo DNA methylation of retrotransposon genes, and many proteins, including PIWI family proteins, play pivotal roles in this process [4–6]. In the embryonic mouse testis, two mouse PIWI proteins, mouse PIWI-like (MILI) and mouse PIWI2 (MIWI2), are involved in the biogenesis of piRNAs through the so-called ping-pong amplification cycle [7–10], and long single-stranded RNAs transcribed from the gene regions of piRNA clusters have been proposed to be the initial material [11–16]. However, it remains unclear whether transcription from the piRNA clusters is required for the biogenesis of piRNAs. To answer this question, we developed a novel artificial piRNA production system by simple expression of sense and antisense EGFP mRNAs in embryonic male germ cells in the piRNA biogenesis phase. EGFP expression was silenced by piRNA-dependent DNA methylation, indicating that concomitant expression of sense and antisense RNA transcripts is necessary and sufficient for piRNA production and subsequent piRNA-dependent gene silencing. In addition, we demonstrated that this artificial piRNA induction paradigm could be applied to an endogenous gene essential for spermatogenesis, DNMT3L [3, 17, 18]. This study not only provides novel insights into the molecular mechanisms of piRNA production, but also presents an innovative strategy for inducing epigenetic modification in germ cells

Alterações oxidativas em portadores da doença de Alzheimer: correlação com os estágios da doença e o quadro cognitivo dos pacientes

The survival of the population has increased gradually and it is correlated with quality of health services and general living conditions, being particularly marked in industrialized countries. The increase in life expectancy affects the incidence of age-associated diseases. Aging is considered a risk factor for the development of neurodegenerative diseases like Alzheimer’s disease (AD). One theory on the pathogenesis of AD postulates that neurodegeneration is the result of oxidative stress and damage to vulnerable cerebral tissues. The fact that aging is a risk factor in AD also reinforces the hypothesis of free radicals involvement, because the effects of their actions can accumulate for years. It is an insidious, progressive disease and is characterized clinically by progressive loss of memory and other cognitive functions, as well as behavioral and social changes. The memory deficit is the main and usually the first symptom of AD, especially with deficiency of retention and recall of new information. The present study aims to evaluate if there are changes in oxidative metabolism detected in the blood of patients with AD, and if there is correlation with different stages of the disease and the patients’ cognitive framework. We evaluated 30 patients with Alzheimer’s disease and 28 subjects in the control group attended at Unit Education and Assistance Physical Therapy and Occupational Therapy at the University of Pará (UEAFTO-UEPA). Oxidative metabolism was assessed by measuring the total antioxidant capacity equivalent to Trolox (TEAC) and measuring the levels of substances that react with thiobarbituric acid (TBARS). Neuropsychological tests were also performed on all participants in the study. No significant correlations were observed in the performance of neuropsychological tests to the levels of TBARS and TEAC in patients with AD. It was observed that the total antioxidant capacity (TAC) was significantly decreased in AD patients compared to controls whatever stage of disease, showing a possible relationship between TAC and AD. In the evaluation of TBARS was a trend toward higher concentrations in AD patients than in control group but the difference was not statistically significant, only the moderate stage was significant when compared with the control group. Evaluation of the lipidic peroxidation through TBARS a biomarker would probably not be suitable for Alzheimer's disease.FAPESPA - Fundação Amazônia de Amparo a Estudos e PesquisasA sobrevida da população tem aumentado de forma progressiva e atribui-se à melhoria da qualidade dos serviços de saúde e das condições gerais de vida, sendo marcante, sobretudo nos países industrializados. Este aumento da expectativa de vida repercute no aumento da incidência de doenças comuns em idades avançadas. O envelhecimento é considerado fator de risco para o desenvolvimento de doenças neurodegenerativas como a doença de Alzheimer (DA). Uma das teorias para a patogênese da DA postula que a neurodegeneração é o resultado de alterações no metabolismo oxidativo com acometimento do tecido cerebral vulnerável. O fato de o envelhecimento ser um fator de risco na DA, reforça também a hipótese da participação dos radicais livres, pois os efeitos de sua ação podem se acumular durante anos. A DA é uma doença insidiosa e progressiva e caracteriza-se clinicamente por uma perda progressiva da memória e de outras funções cognitivas, além de mudanças comportamentais e sociais. O déficit de memória é o principal e usualmente o primeiro sintoma da DA, com comprometimento especialmente da retenção e recordação de novas informações. O presente trabalho visa avaliar se ocorrem alterações no metabolismo oxidativo detectáveis no sangue de pacientes com a DA, e se estas podem ser relacionadas com os diferentes estágios da doença e com o quadro cognitivo dos pacientes. Foram avaliados 30 pacientes com a doença de Alzheimer e 28 indivíduos no grupo controle atendidos na Unidade de Ensino e Assistência de Fisioterapia e Terapia Ocupacional da Universidade do Estado do Pará (UEAFTO-UEPA). O metabolismo oxidativo foi avaliado através da medida da capacidade antioxidante total equivalente ao Trolox (TEAC) e da mensuração dos níveis das substâncias que reagem ao ácido tiobarbitúrico - TBARS. Também foram realizados testes neuropsicológicos em todos os sujeitos participantes do estudo. Não foram observadas correlações significativas no desempenho dos testes neuropsicológicos com os níveis de TBARS e TEAC nos pacientes com a DA. Observou-se que a capacidade antioxidante total (CAOT) estava significativamente diminuída nos pacientes com a DA em comparação com o grupo controle independentemente do estágio da doença, mostrando uma possível relação entre a CAOT e a DA. Na avaliação de TBARS houve uma tendência para maiores concentrações nos pacientes com DA do que no grupo controle, porém a diferença não foi estatisticamente significativa, apenas a fase moderada foi significativa quando comparada com o grupo controle. A avaliação da peroxidação lipídica através dos níveis de TBARS provavelmente não seria um biomarcador adequado para a doença de Alzheimer

HTLV-1, Immune Response and Autoimmunity

Human T-lymphotropic virus type-1 (HTLV-1) infection is associated with adult T-cell leukemia/lymphoma (ATL). Tropical spastic paraparesis/HTLV-1-associated myelopathy (PET/HAM) is involved in the development of autoimmune diseases including Rheumatoid Arthritis (RA), Systemic Lupus Erythematosus (SLE), and Sjögren’s Syndrome (SS). The development of HTLV-1-driven autoimmunity is hypothesized to rely on molecular mimicry, because virus-like particles can trigger an inflammatory response. However, HTLV-1 modifies the behavior of CD4+ T cells on infection and alters their cytokine production. A previous study showed that in patients infected with HTLV-1, the activity of regulatory CD4+ T cells and their consequent expression of inflammatory and anti-inflammatory cytokines are altered. In this review, we discuss the mechanisms underlying changes in cytokine release leading to the loss of tolerance and development of autoimmunity

Formation of multiple pulmonary nodules during treatment with leflunomide

Pulmonary involvement is one of the extra-articular manifestations of rheumatoid arthritis and can be due to the disease itself or secondary to the medications used in order to treat it. We report the case of a 60-year-old woman who had been diagnosed with rheumatoid arthritis and developed multiple pulmonary nodules during treatment with leflunomide

X-linked spinal and bulbar muscular atrophy (Kennedy’s disease): the first case described in the Brazilian Amazon

<div><p>ABSTRACT The X-linked spinal and bulbar muscular atrophy (Kennedy’s disease) is a rare X-linked, recessive, lower motor neuron disease, characterized by weakness, atrophy, and fasciculations of the appendicular and bulbar muscle. The disease is caused by an expansion of the CAG repetition in the androgen receptor gene. Patients with Kennedy’s disease have more than 39 CAG repetitions. We report a case of 57-year-old man, resident of Monte Dourado (PA, Brazil) who complained of brachiocrural paresis evolving for 3 years along with fasciculations and tremors of extremities. In addition, he also developed dysarthria, dysphagia, and sexual dysfunction. The patient clinical picture included gait impairment, global hyporeflexia, proximal muscle atrophy of upper limbs, deviation of the uvula to right during phonation and tongue atrophy with fasciculations. The patient reported that about 30 years ago he had undergone gynecomastia surgery. His electroneuromyography suggested spinal muscular atrophy, and nuclear magnetic resonance imaging showed tapering of the cervical and thoracic spinal cord. Patient’s creatine kinase level was elevated. In view of the findings, an exam was requested to investigate Kennedy’s disease. The exam identified 46 CAG repetitions in the androgen receptor gene, which confirmed the diagnostic suspicion. This was the first case of Kennedy’s disease diagnosed and described in the Brazilian Amazon. To our knowledge only other four papers were published on this disease in Brazilian patients. A brief review is also provided on etiopathogenic, clinical and diagnostic aspects.</p></div

Correction: CT Chest and pulmonary functional changes in patients with HTLV-associated myelopathy in the Eastern Brazilian Amazon.

[This corrects the article DOI: 10.1371/journal.pone.0186055.]

CT Chest and pulmonary functional changes in patients with HTLV-associated myelopathy in the Eastern Brazilian Amazon

<div><p>The aim of this study was to compare computed tomography (CT) scans of chest and lung function among patients with Human T-Lymphotropic Virus Type 1 (HTLV) with and without HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP). In this cross-sectional study performed between January 2013 and June 2016, we included 48 patients with HAM/TSP (19 women and 11 men) and without HAM/TSP (12 women and 6 men). We compared CT findings and lung functions of these groups. Patients who had HAM/TSP had abnormal CT findings (<i>P</i> = 0.000), including more frequent bronchiectasis (<i>P</i> = 0.049), parenchymal bands (<i>P</i> = 0.007), interlobular septal thickening (<i>P</i> = 0.035), and pleural thickening (<i>P</i> = 0.009). In addition, neither patients with HAM/TSP (9/30; 30%) nor the controls (0/18; 0%) had obstructive or restrictive lung disease (<i>P</i> = 0.009). HTLV diagnosis should be considered in all patients with abnormal CT findings in whom no other cause is apparent. It is important to remember that lung disease increases the rates of morbidity and mortality in developing countries.</p></div

Volumes, capacities and flows obtained and predicted for women and men without HAM/TSP.

<p>Volumes, capacities and flows obtained and predicted for women and men without HAM/TSP.</p