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1.
Arch Toxicol ; 93(11): 3219-3228, 2019 11.
Article in English | MEDLINE | ID: mdl-31576414

ABSTRACT

A previous study showed that people living in urban areas are generally exposed to low-frequency noise (LFN) with frequencies below 100 Hz and sound levels of 60-110 dB in daily and occupational environments. Exposure to LFN has been shown to affect balance in humans and mice. However, there is no information about prevention of LFN-mediated imbalance because of a lack of information about the target region based on health risk assessment of LFN exposure. Here, we show that acute exposure to LFN at 100 Hz, 95 dB, but not at 85 dB or 90 dB, for only 1 h caused imbalance in mice. The exposed mice also had decreased cervical vestibular-evoked myogenic potential (cVEMP) with impaired activity of vestibular hair cells. Since imbalance in the exposed mice was irreversible, morphological damage in the vestibules of the exposed mice was further examined. The exposed mice had breakage of the otoconial membrane in the vestibule. LFN-mediated imbalance and breakage of the otoconial membrane in mice were rescued by overexpression of a stress-reactive molecular chaperone, heat shock protein 70 (Hsp70), which has been shown to be induced by exposure of mice to 12 h per day of LFN at 95 dB for 5 days. Taken together, the results of this study demonstrate that acute exposure to LFN at 100 Hz, 95 dB for only 1 h caused irreversible imbalance in mice with structural damage of the otoconial membrane as the target region for LFN-mediated imbalance, which can be rescued by Hsp70.


Subject(s)
Environmental Exposure/adverse effects , Evoked Potentials, Auditory/physiology , HSP70 Heat-Shock Proteins/metabolism , Noise/adverse effects , Sensation Disorders/metabolism , Vestibule, Labyrinth/metabolism , Acoustic Stimulation , Animals , Environmental Exposure/analysis , HSP70 Heat-Shock Proteins/genetics , Mice , Mice, Inbred ICR , Mice, Transgenic , Otolithic Membrane/metabolism , Postural Balance/physiology , Sensation Disorders/physiopathology
2.
Environ Health Prev Med ; 24(1): 39, 2019 Jun 01.
Article in English | MEDLINE | ID: mdl-31153359

ABSTRACT

BACKGROUND: Cervical vestibular evoked myogenic potential (cVEMP) testing is a strong tool that enables objective determination of balance functions in humans. However, it remains unknown whether cVEMP correctly expresses vestibular disorder in mice. OBJECTIVE: In this study, correlations of cVEMP with scores for balance-related behavior tests including rotarod, beam, and air-righting reflex tests were determined in ICR mice with vestibular disorder induced by 3,3'-iminodipropiontrile (IDPN) as a mouse model of vestibular disorder. METHODS: Male ICR mice at 4 weeks of age were orally administered IDPN in saline (28 mmol/kg body weight) once. Rotarod, beam crossing, and air-righting reflex tests were performed before and 3-4 days after oral exposure one time to IDPN to determine balance functions. The saccule and utricles were labeled with fluorescein phalloidin. cVEMP measurements were performed for mice in the control and IDPN groups. Finally, the correlations between the scores of behavior tests and the amplitude or latency of cVEMP were determined with Spearman's rank correlation coefficient. Two-tailed Student's t test and Welch's t test were used to determine a significant difference between the two groups. A difference with p < 0.05 was considered to indicate statistical significance. RESULTS: After oral administration of IDPN at 28 mmol/kg, scores of the rotarod, beam, and air-righting reflex tests in the IDPN group were significantly lower than those in the control group. The numbers of hair cells in the saccule, utricle, and cupula were decreased in the IDPN group. cVEMP in the IDPN group was significantly decreased in amplitude and increased in latency compared to those in the control group. cVEMP amplitude had significant correlations with the numbers of hair cells as well as scores for all of the behavior tests in mice. CONCLUSIONS: This study demonstrated impaired cVEMP and correlations of cVEMP with imbalance determined by behavior tests in a mouse model of vestibular disorder.


Subject(s)
Postural Balance/physiology , Sensation Disorders/physiopathology , Vestibular Diseases/physiopathology , Vestibular Evoked Myogenic Potentials/physiology , Animals , Behavior, Animal/drug effects , Behavior, Animal/physiology , Disease Models, Animal , Hair Cells, Vestibular/pathology , Male , Mice , Mice, Inbred ICR , Nitriles/adverse effects , Postural Balance/drug effects , Saccule and Utricle/pathology , Sensation Disorders/chemically induced , Vestibular Diseases/chemically induced , Vestibular Diseases/diagnosis , Vestibular Diseases/pathology , Vestibular Evoked Myogenic Potentials/drug effects , Vestibular Function Tests
3.
Sci Rep ; 9(1): 9028, 2019 06 21.
Article in English | MEDLINE | ID: mdl-31227759

ABSTRACT

Well water for drinking with increased levels of iron in arsenic-polluted areas has been reported worldwide. Oral exposure to arsenic has been shown to be associated with hearing loss, while there is no evidence for an association between excessive exposure to iron and hearing loss in humans. In this study, we determined iron and arsenic levels in biological samples and hearing levels by pure tone audiometry (PTA) in subjects in a control area and an arsenic-polluted area in Bangladesh. The iron level in well water in the arsenic-polluted area was significantly higher than that in piped supply water in the control area. Subjects in the polluted area (n = 109), who had higher iron and arsenic levels in hair and toenails than those in subjects in the control area (n = 36), had an increased risk of hearing loss at 8 kHz and 12 kHz after adjustments for age, gender, smoking and BMI. Significant associations of the exposure group with hearing loss at 8 kHz and 12 kHz remained after further adjustment for arsenic levels in toenails and hair. Thus, this pilot study showed that excessive exposure to iron via drinking water is a potential risk for hearing loss in humans.


Subject(s)
Arsenic/analysis , Hearing Loss/diagnosis , Iron/analysis , Water Pollutants, Chemical/analysis , Water Pollution/analysis , Water Wells , Adult , Arsenic/metabolism , Audiometry, Pure-Tone/methods , Bangladesh , Drinking Water/analysis , Drinking Water/standards , Female , Hair/chemistry , Hearing Loss/etiology , Humans , Iron/metabolism , Male , Nails/chemistry , Pilot Projects , ROC Curve , Water Pollutants, Chemical/metabolism , Water Pollution/adverse effects , Young Adult
4.
PLoS One ; 13(7): e0198743, 2018.
Article in English | MEDLINE | ID: mdl-29975704

ABSTRACT

Arsenic (As) pollution in drinking water is a worldwide health risk for humans. We previously showed hearing loss in young people who live in areas of As-polluted drinking water and in young mice orally treated with As. In this study, we epidemiologically examined associations between As levels in toenails and hearing in 145 Bangladeshi aged 12-55 years in 2014. Levels of As in toenails, but not those in urine, were shown to be significantly correlated with hearing loss at 4 kHz [odds ratio (OR) = 4.27; 95% confidence interval (CI): 1.51, 12.05], 8 kHz (OR = 3.91; 95% CI: 1.47, 10.38) and 12 kHz (OR = 4.15; 95% CI: 1.55, 11.09) by multivariate analysis with adjustments for age, sex, smoking and BMI. Our experimental study further showed a significant association between As levels in inner ears and nails (r = 0.8113, p = 0.0014) in mice orally exposed to As, suggesting that As level in nails is a suitable index to assess As level in inner ears. Taken together, the results of our study suggest that As level in nails could be a convenient and non-invasive biomarker for As-mediated hearing loss in humans.


Subject(s)
Arsenic/isolation & purification , Hearing Loss/pathology , Nails/chemistry , Water Pollutants, Chemical/isolation & purification , Adolescent , Adult , Animals , Arsenic/adverse effects , Arsenic/chemistry , Bangladesh/epidemiology , Child , Drinking Water/chemistry , Ear, Inner/chemistry , Ear, Inner/pathology , Environmental Exposure , Female , Hearing Loss/chemically induced , Hearing Loss/epidemiology , Humans , Male , Mice , Middle Aged , Multivariate Analysis , Water Pollutants, Chemical/chemistry , Young Adult
5.
Biomarkers ; 23(6): 533-539, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29619852

ABSTRACT

PURPOSE: Elevated hearing thresholds from high frequencies are known to be one of the hallmarks of age-related hearing loss. Our recent study showed accumulation of manganese (Mn) in inner ears resulting in acceleration of age-related hearing loss in mice orally exposed to Mn. However, there is no evidence showing an association between Mn in non-invasive biological samples and hearing loss in humans evaluated by pure tone audiometry (PTA). In this study, we evaluated Mn in non-invasive biological samples as a possible biomarker for hearing loss in humans. MATERIALS AND METHODS: We determined hearing levels by PTA and Mn levels in toenails, hair and urine with an inductively coupled plasma mass spectrometer (ICP-MS) in 145 healthy subjects in Bangladesh. RESULTS: Multivariable analyses showed that Mn levels in toenails, but not in hair and urine samples, were significantly associated with hearing loss at 8 kHz and 12 kHz. Moreover, our experimental study showed a significant correlation between Mn levels in inner ears and nails, but not hair, in mice orally exposed to Mn. CONCLUSIONS: The results provide novel evidence that Mn in toenails is a possible biomarker for hearing loss at high frequencies in humans.


Subject(s)
Biomarkers/analysis , Hearing Loss/metabolism , Manganese/analysis , Nails/chemistry , Adolescent , Adult , Animals , Audiometry, Pure-Tone/methods , Bangladesh , Child , Female , Hair/chemistry , Hearing Loss/diagnosis , Humans , Male , Manganese/urine , Mass Spectrometry/methods , Mice, Inbred C57BL , Middle Aged , Multivariate Analysis , Young Adult
6.
Hear Res ; 363: 49-54, 2018 06.
Article in English | MEDLINE | ID: mdl-29519617

ABSTRACT

Previous studies showed that people in urban areas are possibly exposed to 60-110 dB of low frequency noise (LFN) defined as noise of ≤100 Hz in their daily life. Previous studies also showed increased health risks by exposure to high levels (130-140 dB) of LFN in animals. However, little is known about the health effects of exposure to an ordinary level of LFN. We biochemically and immunohistochemically assessed the effects of exposure to inaudible LFN for mice (12 h/day of 100 Hz LFN at 95 dB for 5 days), at a level to which people are possibly exposed in daily life, on a murine inner ear by targeting 9 stress-reactive molecules. There was more than a 5-fold increased transcript level of heat shock protein 70 (Hsp70) in the whole inner ear exposed to LFN. However, the transcript levels of the other 8 stress-reactive molecules including Hsp27 and Hsp90 were comparable in LFN-exposed and unexposed murine inner ears. Only the transcript level of Cebpß among the previously reported 4 transcriptional activators for Hsp70 expression was more than 3-fold increased by LFN exposure. Hsp70 transcript expression levels in the inner ears 3 days after LFN exposure were comparable to those in unexposed inner ears. The protein level of Hsp70, but not the levels of Hsp27 and Hsp90, was also increased in the vestibule by LFN exposure. However, hearing levels as well as expression levels of Hsp70 protein in the cochleae were comparable in LFN-exposed mice and unexposed mice. Our results demonstrated that the inner ear might be one of the organs that is negatively affected by stress from inaudible LFN exposure. Moreover, LFN exposure might increase Hsp70 expression level via Cebpß in the inner ear. Thus, Hsp70 and Cebpß levels could be candidates of biomarkers for response to LFN exposure.


Subject(s)
Cochlea/metabolism , HSP70 Heat-Shock Proteins/metabolism , Hearing , Noise/adverse effects , Acoustic Stimulation , Animals , Biomarkers/metabolism , CCAAT-Enhancer-Binding Protein-beta/genetics , CCAAT-Enhancer-Binding Protein-beta/metabolism , Evoked Potentials, Auditory, Brain Stem , Female , HSP70 Heat-Shock Proteins/genetics , Male , Mice, Inbred ICR , Time Factors , Up-Regulation
7.
J Expo Sci Environ Epidemiol ; 28(1): 64-68, 2018 01.
Article in English | MEDLINE | ID: mdl-27966667

ABSTRACT

There has been no report showing the effect of arsenic level on digitized skin pigmentation level, a typical diagnostic marker for arsenicosis. Correlations among history of drinking well water, arsenic levels in hair and toenails, and digitalized skin pigmentation levels (L*-value) in sunlight-exposed (forehead) and unexposed (sole) skin areas digitally evaluated by using a reflectance spectrophotometer were examined in 150 residents of Bangladesh. Univariate analysis showed that arsenic levels in hair and toenails of subjects with a history of drinking well water were 10.6-fold and 7.1-fold higher, respectively, than those in subjects without a history of drinking well water. The mean L*-value of foreheads, but not that of soles, in subjects with a history of drinking well water was 1.15-fold lower (more pigmented) than that in subjects without a history of drinking well water. Significant correlations were found between duration of drinking well water and arsenic concentrations in hair (r=0.63; P<0.01) and toenails (r=0.60; P<0.01). Multivariate analysis showed that the arsenic levels in hair and toenails and the duration of drinking well water were strongly correlated with the digitized pigmented level of the forehead but not that of the sole. An increase in the duration of drinking well water may increase hyperpigmentation in the forehead, but not that in the sole, through an increased arsenic level in the human body as shown in cutaneous appendicular organs (hair and toenails).


Subject(s)
Arsenic/adverse effects , Drinking Water/chemistry , Hair/chemistry , Hyperpigmentation/chemically induced , Nails/chemistry , Water Pollutants, Chemical/adverse effects , Adolescent , Adult , Arsenic Poisoning , Bangladesh/epidemiology , Child , Environmental Exposure/adverse effects , Female , Foot/pathology , Forehead/pathology , Humans , Hyperpigmentation/epidemiology , Male , Middle Aged , Multivariate Analysis , Skin , Spectrophotometry , Surveys and Questionnaires , Water Pollutants, Chemical/analysis , Young Adult
8.
Sci Rep ; 7(1): 6844, 2017 07 28.
Article in English | MEDLINE | ID: mdl-28754998

ABSTRACT

There is no information on the association between oral exposure to arsenic (As) and hearing loss in humans or mice. In this combined epidemiological study and experimental study, the association of oral exposure to As with hearing loss in people aged 12-29 years and young mice was examined. Subjects in the exposure group (n = 48), who were drinking tube well water contaminated with As, showed significantly higher risks of hearing loss at 4 kHz [odds ratio (OR) = 7.60; 95% confidence interval (CI): 1.56, 57.88], 8 kHz (OR = 5.00; 95% CI: 1.48, 18.90) and 12 kHz (OR = 8.72; 95% CI: 2.09, 47.77) than did subjects in the control group (n = 29). We next performed an experiment in which young mice were exposed to As via drinking water at 22.5 mg/L, which is a much greater concentration than that in human studies. The exposure group showed hearing loss and accumulation of As in inner ears. Ex vivo exposure of the organ of Corti from mice exposed to As significantly decreased the number of auditory neurons and fibers. Thus, our combined study showed that oral exposure to As caused hearing loss in young people and young mice.


Subject(s)
Arsenic Poisoning/complications , Arsenic/toxicity , Hearing Loss/chemically induced , Water Pollutants, Chemical/toxicity , Adolescent , Adult , Animals , Arsenic/analysis , Arsenic/pharmacokinetics , Arsenic Poisoning/etiology , Child , Drinking Water/chemistry , Ear, Inner/drug effects , Ear, Inner/metabolism , Female , Humans , Male , Mice , Mice, Inbred C57BL , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/pharmacokinetics
9.
Neurotox Res ; 32(4): 661-670, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28730349

ABSTRACT

Previous studies showed that overexposure to manganese causes parkinsonism, a disorder of dopaminergic neurons. Previous studies also showed that activity of c-RET kinase controls dopamine production through regulation of tyrosine hydroxylase (TH) expression, suggesting the involvement of c-RET in the development of parkinsonism. To our knowledge, however, there is no report showing a correlation between manganese-mediated parkinsonism and c-RET. In this study, we examined the effect of manganese on the expression and/or activation levels of c-RET and TH in human TH-expressing cells (TGW cells). We first found that treatment with 30 and 100 µM manganese resulted in reduction of c-RET transcript level and degradation of c-RET protein through promotion of ubiquitination. We then examined the biological significance of manganese-mediated decrease of c-RET protein expression. Decreased TH expression with decreased c-RET kinase activity was observed in c-RET protein-depleted TGW cells by treatment with manganese (30 µM) as well as by c-RET siRNA transfection. Since TH protein has been shown to be involved in the dopamine-producing pathway in previous studies, our results indicate the possibility that manganese-mediated reduction of TH expression and phosphorylation via decreased expression of c-RET protein in neural cells is involved in parkinsonism induced by manganese.


Subject(s)
Dopamine/metabolism , Manganese/metabolism , Proto-Oncogene Proteins c-ret/metabolism , Tyrosine 3-Monooxygenase/metabolism , Humans , Mesencephalon/metabolism , Neurons/drug effects , Phosphorylation/drug effects
10.
Arch Toxicol ; 91(11): 3507-3516, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28470405

ABSTRACT

Chronic exposure to arsenic is associated with various diseases in humans. Skin hyperpigmentation is the most sensitive objective symptom for patients with arsenicosis. However, there is very limited information about the mechanism of arsenic-mediated skin hyperpigmentation in vivo. In this study, hairless homozygous mice (Hr/Hr-mice) that drank water containing 3 and 30 µM arsenic for 2 months developed skin hyperpigmentation with increased levels of arsenic and number of melanocytes in the skin. Since it is possible for humans to be exposed to 3 µM of arsenic in well drinking water, our results suggest that the Hr/Hr-mice could be a novel model sensitively reflecting arsenic-mediated skin hyperpigmentation. We then analyzed the mechanism of arsenic-mediated skin hyperpigmentation. The epidermis of Hr/Hr-mice and human HaCaT skin keratinocytes exposed to arsenic for 2 and 4 months, respectively, showed 5.4-21.5-fold increased levels of endothelin-1 (ET-1) expression via NF-kappa B activation. Coexposure of primary normal human epithelial melanocytes to arsenic and ET-1 activated their proliferation and melanin synthesis with increased levels of MITF-M and ET-1 receptor expression. Our results suggest that interaction between keratinocytes and melanocytes in the skin through ET-1 and its receptor contributes to arsenic-mediated skin pigmentation, a hallmark of arsenicosis.


Subject(s)
Arsenic/toxicity , Endothelin-1/metabolism , Hyperpigmentation/chemically induced , NF-kappa B/metabolism , Animals , Cell Line , Disease Models, Animal , Drinking Water/adverse effects , Epidermal Cells , Epidermis/drug effects , Epidermis/metabolism , Homozygote , Humans , Hyperpigmentation/metabolism , Keratinocytes/drug effects , Keratinocytes/metabolism , Keratinocytes/pathology , Melanocytes/drug effects , Melanocytes/metabolism , Mice, Hairless , Receptor, Endothelin B/genetics , Receptor, Endothelin B/metabolism
11.
Front Behav Neurosci ; 11: 30, 2017.
Article in English | MEDLINE | ID: mdl-28275341

ABSTRACT

General electric devices and ventilation systems are known to generate low frequency noise (LFN) with frequencies of <100 Hz. Previous studies showed that exposure to LFN caused impairments of balance in humans and mice during adulthood. On the other hand, a previous study showed that noise levels in the neonatal intensive care unit (NICU) were greater than those in general home or office environments. Therefore, it is possible that neonates have a potential risk to be exposed to LFN in the NICU. However, the risk of neonatal exposure to LFN remains unclear in humans and mice. In this study, male ICR mice were exposed to LFN at 100 Hz for 4 weeks after birth and then subjected to rotarod and beam crossing tests in order to assess LFN-mediated risk of imbalance during the neonatal period. Exposure to LFN at 70 dB, but not exposure to LFN up to 60 dB, during the neonatal period significantly decreased performance scores for rotarod and beam crossing tests compared to the scores of the control group. The number of calbindin-positive hair cells in the saccule and utricle was decreased in mice exposed to LFN at 70 dB for 4 weeks in the neonatal phase. Cessation of exposure for 10 weeks did not result in recovery of the decreased performance in rotarod and beam crossing tests. Thus, our results suggest that 70 dB is a possible threshold for exposure to LFN for 4 weeks during the neonatal period causing unrecoverable imbalance in mice.

12.
Nihon Eiseigaku Zasshi ; 72(1): 38-42, 2017.
Article in Japanese | MEDLINE | ID: mdl-28154359

ABSTRACT

The inner ears contain the organ of Corti, vestibule and semicircular canal. The organ of Corti is crucial for hearing, while the vestibule and semicircular canal play important roles in maintaining balance. Exposure to noise at excessive levels is known to cause damages of the inner ears, resulting in noise-induced hearing loss. On the other hand, noise levels (dB) are used for the evaluation of health risks by exposure to noise, although noise consists of sound with broad frequencies (Hz). Thus, information about the frequency-dependent effect of noise on health is largely unknown. In this review, we first introduce noise-induced hearing loss caused by exposure to audible noise. We then describe the imbalance in mice exposed to low-frequency noise (100 Hz).


Subject(s)
Ear, Inner , Environmental Exposure/adverse effects , Hearing Loss, Noise-Induced/etiology , Labyrinth Diseases/etiology , Noise/adverse effects , Animals , Ear, Inner/physiology , Ear, Inner/physiopathology , Health Status Indicators , Hearing , Humans , Mice , Postural Balance , Risk
13.
J Water Health ; 14(6): 1032-1040, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27959882

ABSTRACT

Since well water utilized for domestic purposes in the Red River Delta of North Vietnam has been reported to be polluted by arsenic, barium, iron, and manganese, household sand filters consisting of various components are used. Information regarding the effectiveness of various sand filters for removal of the four toxic elements in well water is limited. In this study, arsenic levels in 13/20 of well water samples and 1/7 of tap water samples exceeded World Health Organization (WHO) health-based guideline value for drinking water. Moreover, 2/20, 6/20, and 4/20 of well water samples had levels exceeding the present and previous guideline levels for barium, iron, and manganese, respectively. Levels of iron and manganese, but not arsenic, in well water treated by sand filters were lower than those in untreated water, although previous studies showed that sand filters removed all of those elements from water. A low ratio of iron/arsenic in well water may not be sufficient for efficient removal of arsenic from household sand filters. The levels of barium in well water treated by sand filters, especially a filter composed of sand and charcoal, were significantly lower than those in untreated water. Thus, we demonstrated characteristics of sand filters in North Vietnam.


Subject(s)
Arsenic/analysis , Drinking Water/analysis , Filtration/methods , Silicon Dioxide/chemistry , Water Pollutants, Chemical/analysis , Water Purification/methods , Environmental Monitoring , Vietnam
14.
Sci Rep ; 6: 36306, 2016 11 08.
Article in English | MEDLINE | ID: mdl-27824154

ABSTRACT

Despite the fact that manganese (Mn) is known to be a neurotoxic element relevant to age-related disorders, the risk of oral exposure to Mn for age-related hearing loss remains unclear. In this study, we orally exposed wild-type young adult mice to Mn (Mn-exposed WT-mice) at 1.65 and 16.50 mg/L for 4 weeks. Mn-exposed WT-mice showed acceleration of age-related hearing loss. Mn-exposed WT-mice had neurodegeneration of spiral ganglion neurons (SGNs) with increased number of lipofuscin granules. Mn-exposed WT-mice also had increased hypoxia-inducible factor-1 alpha (Hif-1α) protein with less hydroxylation at proline 564 and decreased c-Ret protein in SGNs. Mn-mediated acceleration of age-related hearing loss involving neurodegeneration of SGNs was rescued in RET-transgenic mice carrying constitutively activated RET. Thus, oral exposure to Mn accelerates age-related hearing loss in mice with Ret-mediated neurodegeneration of SGNs.


Subject(s)
Aging/drug effects , Hearing Loss/chemically induced , Hypoxia-Inducible Factor 1, alpha Subunit/metabolism , Manganese/toxicity , Proto-Oncogene Proteins c-ret/metabolism , Aging/metabolism , Animals , Disease Models, Animal , Hearing Loss/metabolism , Hearing Loss/pathology , Hydroxylation , Mice , Mice, Transgenic , Nerve Degeneration , Phosphorylation , Proline/metabolism , Spiral Ganglion/drug effects , Spiral Ganglion/metabolism , Spiral Ganglion/pathology , Up-Regulation
15.
Br J Cancer ; 113(4): 669-79, 2015 Aug 11.
Article in English | MEDLINE | ID: mdl-26196182

ABSTRACT

BACKGROUND: Growth arrest and DNA damage-inducible protein 34 (GADD34/Ppp1r15a) is a family of GADD proteins that are induced by DNA damage. GADD34 protein has been suggested to regulate inflammation or host defense systems. However, the in vivo function of GADD34 in inflammation is still unclear. Long lasting inflammation, such as that seen in Crohn's disease and ulcerative colitis, is associated with a higher incidence of colorectal cancer (CRC). METHODS: Using a colitis-associated cancer model, we analysed GADD34-deficient (KO) mice to study the effect of GADD34 on colitis and colorectal tumorigenesis. RESULTS: We found a higher incidence of CRC in wild-type (WT) mice than in GADD34KO mice. Moreover, dextran sodium sulfate (DSS)-induced inflammatory responses were downregulated by GADD34 deficiency. The expression of pro-inflammatory mediators such as TNFα, IL-6, and iNOS/NOS2 was higher in the colons of WT mice than GADD34KO mice. IL-6 is known to activate STAT3 signalling in colonic epithelial cells and subsequently induced epithelial proliferation. We found that IL-6-STAT3 signalling and epithelial proliferation were higher in WT mice compared with GADD34KO mice. CONCLUSIONS: These results indicated that GADD34 upregulated pro-inflammatory mediator production leading to a higher tumour burden following azoxymethane (AOM)/DSS treatment.


Subject(s)
Colonic Neoplasms/metabolism , Inflammation/metabolism , Protein Phosphatase 1/metabolism , Animals , Cell Proliferation/physiology , Cell Transformation, Neoplastic/metabolism , Cell Transformation, Neoplastic/pathology , Colitis/metabolism , Colitis/pathology , Colonic Neoplasms/pathology , DNA Damage/physiology , Disease Models, Animal , Epithelial Cells/metabolism , Epithelial Cells/pathology , Female , Inflammation/pathology , Interleukin-6/metabolism , Mice , Mice, Inbred C57BL , Nitric Oxide Synthase Type II/metabolism , STAT3 Transcription Factor/metabolism , Signal Transduction/physiology , Tumor Necrosis Factor-alpha/metabolism , Up-Regulation/physiology
16.
Sci Rep ; 5: 8327, 2015 Feb 09.
Article in English | MEDLINE | ID: mdl-25659802

ABSTRACT

Autophagy is a common physiological function in all eukaryotes. The process is induced by depletion of nutrients including amino acids. GADD34 is expressed following DNA damage, ER stresses and amino acid deprivation. Here, we investigated the effects of GADD34 on autophagy and cell activation in macrophages. The deprivation of tyrosine and cysteine markedly induced the expression of GADD34 in macrophages. LPS stimulation combined with tyrosine/cysteine-deprivation initially activated macrophages, but then shifted to cell death in late phase of stimulation. When LPS stimulation was combined with tyrosine/cysteine-deprivation, a deficiency of GADD34 enhanced cell activation signaling such as Src-family, Erk1/2, p38 MAPK and Akt. In the late phase of stimulation, a deficiency of GADD34 increased apoptosis more than that in wild-type macrophages. Further we found that mTOR-S6K signaling was highly enhanced in GADD34-deficient macrophages compared with wild-type cells when cells were treated by LPS combined with tyrosine/cysteine-deprivation. LC3-II was increased by LPS stimulation combined with tyrosine/cysteine-deprivation. Defective GADD34 reduced LC3-II and autophagosome formation induced by LPS-stimulation and tyrosine/cysteine-deprivation compared with that seen in wild-type macrophages. These results indicates that GADD34 enhances autophagy and suppresses apoptosis stimulated by LPS combined with amino acid deprivation through regulation of mTOR signaling pathway in macrophages.


Subject(s)
Apoptosis/genetics , Macrophage Activation/genetics , Macrophages/metabolism , Protein Phosphatase 1/genetics , Animals , Autophagy/genetics , Caspase 3/metabolism , Cell Line , Cysteine/metabolism , Cysteine/pharmacology , Gene Expression , Gene Knockdown Techniques , Humans , Lipopolysaccharides/immunology , Macrophage Activation/immunology , Macrophages/drug effects , Macrophages/immunology , Mice , Mice, Knockout , Protein Phosphatase 1/metabolism , Signal Transduction , Sirolimus/pharmacology , TOR Serine-Threonine Kinases/metabolism , Tyrosine/metabolism , Tyrosine/pharmacology
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