Inflammaging is known to be an aging-associated chronic, low-grade inflammatory state that significantly influences the pathophysiology of various age-related diseases, including those affecting oral health. This review explores the molecular and cellular mechanisms of inflammaging and its implications in oral pathology. We will review key factors contributing to inflammaging, including cellular senescence, and immune dysregulation, all of which induce pro-inflammatory cytokines and reactive oxygen species (ROS). These inflammatory mediators affect oral tissues, predisposing individuals to chronic conditions such as periodontitis, and dental pulp inflammation. Additionally, we will briefly discuss how the oral microbiome is involved in the regulation of inflammaging. Understanding the molecular pathways of inflammaging may provide valuable insights not only into oral health but also into potential health strategies for the aging population.

Inflammaging is known to be an aging-associated chronic, low-grade inflammatory state that significantly influences the pathophysiology of various age-related diseases, including those affecting oral health. This review explores the molecular and cellular mechanisms of inflammaging and its implications in oral pathology. We will review key factors contributing to inflammaging, including cellular senescence, and immune dysregulation, all of which induce pro-inflammatory cytokines and reactive oxygen species (ROS). These inflammatory mediators affect oral tissues, predisposing individuals to chronic conditions such as periodontitis, and dental pulp inflammation. Additionally, we will briefly discuss how the oral microbiome is involved in the regulation of inflammaging. Understanding the molecular pathways of inflammaging may provide valuable insights not only into oral health but also into potential health strategies for the aging population.

Inflammaging is known to be an aging-associated chronic, low-grade inflammatory state that significantly influences the pathophysiology of various age-related diseases, including those affecting oral health. This review explores the molecular and cellular mechanisms of inflammaging and its implications in oral pathology. We will review key factors contributing to inflammaging, including cellular senescence, and immune dysregulation, all of which induce pro-inflammatory cytokines and reactive oxygen species (ROS). These inflammatory mediators affect oral tissues, predisposing individuals to chronic conditions such as periodontitis, and dental pulp inflammation. Additionally, we will briefly discuss how the oral microbiome is involved in the regulation of inflammaging. Understanding the molecular pathways of inflammaging may provide valuable insights not only into oral health but also into potential health strategies for the aging population.

Inflammaging is known to be an aging-associated chronic, low-grade inflammatory state that significantly influences the pathophysiology of various age-related diseases, including those affecting oral health. This review explores the molecular and cellular mechanisms of inflammaging and its implications in oral pathology. We will review key factors contributing to inflammaging, including cellular senescence, and immune dysregulation, all of which induce pro-inflammatory cytokines and reactive oxygen species (ROS). These inflammatory mediators affect oral tissues, predisposing individuals to chronic conditions such as periodontitis, and dental pulp inflammation. Additionally, we will briefly discuss how the oral microbiome is involved in the regulation of inflammaging. Understanding the molecular pathways of inflammaging may provide valuable insights not only into oral health but also into potential health strategies for the aging population.

Background: Phosphatidylinositol 3-kinase (PI3K) regulates cellular development and energy homeostasis. However, the roles of its subunits in organ development remain largely unknown. Methods: We explored the roles of PI3K catalytic subunits in steroidogenic factor 1 (SF1)-expressing cells through knockout (KO) of the p110α and p110β subunits. Results: We examined mice with a double KO of p110α and p110β in SF1-expressing cells (p110αβ KOSF1). Although these animals exhibited no significant changes in the development of the ventromedial hypothalamus, we noted pronounced hypotrophy in the adrenal cortex, testis, and ovary. Additionally, corticosterone and aldosterone levels were significantly reduced. The absence of these subunits also resulted in decreased body weight and survival rate, along with impaired glucose homeostasis, in p110αβ KOSF1 mice. Conclusion The data demonstrate the specific roles of PI3K catalytic subunits in the development and function of SF1-expressing organs.

Background: As the number of large-scale studies involving multiple organizations producing data has steadily increased, an integrated system for a common interoperable format is needed. In response to the coronavirus disease 2019 (COVID-19) pandemic, a number of global efforts are underway to develop vaccines and therapeutics. We are therefore observing an explosion in the proliferation of COVID-19 data, and interoperability is highly requested in multiple institutions participating simultaneously in COVID-19 pandemic research. Results: In this study, a laboratory information management system (LIMS) approach has been adopted to systemically manage various COVID-19 non-clinical trial data, including mortality, clinical signs, body weight, body temperature, organ weights, viral titer (viral replication and viral RNA), and multiorgan histopathology, from multiple institutions based on a web interface. The main aim of the implemented system is to integrate, standardize, and organize data collected from laboratories in multiple institutes for COVID-19 non-clinical efficacy testings. Six animal biosafety level 3 institutions proved the feasibility of our system. Substantial benefits were shown by maximizing collaborative high-quality non-clinical research. Conclusions This LIMS platform can be used for future outbreaks, leading to accelerated medical product development through the systematic management of extensive data from non-clinical animal studies.

The zoonotic transmission of viral diseases to humans is a serious public health concern. Pigs are frequently a major reservoir for several zoonotic viral diseases. Therefore, periodic surveillance is needed to determine the infection rates of zoonotic diseases in domestic pigs. Hepatitis E virus (HEV), rotavirus, sapovirus (SaV), and norovirus (NoV) are potential zoonotic viruses. In this study, 296 fecal samples were collected from weaned piglets and growing pigs in 13 swine farms, and the viral RNA was extracted. Partial viral genomes were amplified by reverse transcription-polymerase chain reaction (PCR) or nested-PCR using virusspecific primer sets under different PCR conditions. HEV-3, rotavirus A, and SaV genogoup 3 were detected from 11.5, 2.7, and 3.0% of the samples, respectively. On the other hand, NoV was not detected in any of the samples. Genetic analysis indicated that the nucleotide sequences of swine HEV-3 and rotavirus A detected in this study were closely related to those of human isolates. However, swine SaV was distant from the human strains. These results suggest that HEV-3 and rotavirus A can be transmitted from pigs to humans. Therefore, strict preventive measures should be implemented by workers in the swine industry to prevent infections with HEV-3 and rotavirus A excreted from pigs.

A novel porcine circovirus 3 (PCV3) was first detected in pigs showing porcine dermatitis and nephropathy syndrome, reproductive failure, and multisystemic inflammation in the USA. Herein, we report on PCV3 as a potential etiological agent of clinical signs, reproductive failure and respiratory distress on Korean pig farms, based on in situ hybridization, pathological, and molecular findings. Confirmation of the presence of PCV3 may increase co-infection with other causative agents of disease in Korean pig herds, indicating the need for further systemic investigation of pathogenicity and of multiple infections with PCV2 genotypes and bacteria, and the development of an effective PCV3 vaccine.
Aborted Fetus ; Agriculture ; Bacteria ; Circovirus ; Coinfection ; Dermatitis ; Genotype ; In Situ Hybridization ; Inflammation ; Korea ; Swine ; Virulence

¹⁸F-AV-1451 is a tau PET ligand that has high affinity for paired helical filament tau. However, various off-target bindings unrelated to tau have also been reported. Herein, we report a case of 83-year-old woman, who showed abnormal uptake of AV-1451 that was shown to be subacute infarction. Clinicians should recognize that increased uptake of AV-1451 may be related to stroke.
Aged, 80 and over ; Female ; Humans ; Infarction* ; Stroke

OBJECTIVE: Neurodegeneration with brain iron accumulation (NBIA) represents a group of inherited movement disorders characterized by iron accumulation in the basal ganglia. Recent advances have included the identification of new causative genes and highlighted the wide phenotypic variation between and within the specific NBIA subtypes. This study aimed to investigate the current status of NBIA in Korea. METHODS: We collected genetically confirmed NBIA patients from twelve nationwide referral hospitals and from a review of the literature. We conducted a study to describe the phenotypic and genotypic characteristics of Korean adults with atypical pantothenate kinase-associated neurodegeneration (PKAN). RESULTS: Four subtypes of NBIA including PKAN (n = 30), PLA2G6-related neurodegeneration (n = 2), beta-propeller protein-associated neurodegeneration (n = 1), and aceruloplasminemia (n = 1) have been identified in the Korean population. The clinical features of fifteen adults with atypical PKAN included early focal limb dystonia, parkinsonism-predominant feature, oromandibular dystonia, and isolated freezing of gait (FOG). Patients with a higher age of onset tended to present with parkinsonism and FOG. The p.R440P and p.D378G mutations are two major mutations that represent approximately 50% of the mutated alleles. Although there were no specific genotype-phenotype correlations, most patients carrying the p.D378G mutation had a late-onset, atypical form of PKAN. CONCLUSIONS: We found considerable phenotypic heterogeneity in Korean adults with atypical PKAN. The age of onset may influence the presentation of extrapyramidal symptoms.
Adult ; Age of Onset ; Alleles ; Basal Ganglia ; Brain ; Dystonia ; Freezing ; Gait ; Gene Frequency ; Genetic Association Studies ; Humans ; Iron ; Korea ; Movement Disorders ; Neurodegenerative Diseases ; Pantothenate Kinase-Associated Neurodegeneration* ; Parkinsonian Disorders ; Phenotype ; Population Characteristics* ; Referral and Consultation ; Weather