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1.
J Cell Physiol ; 238(10): 2253-2266, 2023 Oct.
Article in English | MEDLINE | ID: mdl-37565627

ABSTRACT

The skeletal muscle is a tissue that shows remarkable plasticity to adapt to various stimuli. The development and regeneration of skeletal muscles are regulated by numerous molecules. Among these, we focused on Rab44, a large Rab GTPase, that has been recently identified in immune cells and osteoclasts. Recently, bioinformatics data has revealed that Rab44 is upregulated during the myogenic differentiation of myoblasts into myotubes in C2C12 cells. Thus, Rab44 may be involved in myogenesis. Here, we have investigated the effects of Rab44 deficiency on the development and regeneration of skeletal muscle in Rab44 knockout (KO) mice. Although KO mice exhibited body and muscle weights similar to those of wild-type (WT) mice, the histochemical analysis showed that the myofiber cross-sectional area (CSA) of KO mice was significantly smaller than that of WT mice. Importantly, the results of muscle regeneration experiments using cardiotoxin revealed that the CSA of KO mice was significantly larger than that of WT mice, suggesting that Rab44 deficiency promotes muscle regeneration. Consistent with the in vivo results, in vitro experiments indicated that satellite cells derived from KO mice displayed enhanced proliferation and differentiation. Mechanistically, KO satellite cells exhibited an increased mechanistic target of rapamycin complex 1 (mTORC1) signaling compared to WT cells. Additionally, enhanced cell surface transport of myomaker and myomixer, which are essential membrane proteins for myoblast fusion, was observed in KO satellite cells compared to WT cells. Therefore, Rab44 deficiency enhances muscle regeneration by modulating the mTORC1 signaling pathway and transport of fusogenic regulators.

2.
J Dent Sci ; 18(3): 985-990, 2023 Jul.
Article in English | MEDLINE | ID: mdl-37404625

ABSTRACT

Background/purpose: The application of liner type denture adhesives containing ethyl alcohol (EtOH) may result in the person being considered a drunk driver, which is a social problem. This study measured the amount of EtOH loss from the materials and its effect on breath alcohol concentration (BrAC). Materials and methods: The amount of EtOH loss of three liner type denture adhesives was measured using a gas chromatograph-mass spectrometer. Five specimens were measured for each material. The BrAC of ten participants who wore the palatal plate lined with the material having the highest amount of EtOH elution was also determined using an alcohol detector every 5 min for 60 min. The threshold for drunk driving was a BrAC of 0.15 mg/L or more. Results: Significant differences were found in the amount of EtOH elution among the three materials. For all materials, the elution amount from the start of immersion to 30 min was significantly larger than that of the following 30 min (P < 0.05). BrAC values of the participants reached their maxima 5 min after insertion of the materials, and 80% of participants surpassed the threshold for drunk driving. However, no participants reached the threshold for drunk driving after 50 min. Conclusion: The results suggest that a determination of drunk drinking will not be made when 1 h or more has passed after insertion of a denture lined with a liner type denture adhesive into the mouth, though a determination of drunk driving may exist due to EtOH from the materials.

3.
Int J Mol Sci ; 24(2)2023 Jan 04.
Article in English | MEDLINE | ID: mdl-36674510

ABSTRACT

Rab44 was recently identified as an atypical Rab GTPase that possesses EF-hand and coiled-coil domains at the N-terminus, and a Rab-GTPase domain at the C-terminus. Rab44 is highly expressed in immune-related cells such as mast cells, macrophages, osteoclasts, and granulocyte-lineage cells in the bone marrow. Therefore, it is speculated that Rab44 is involved in the inflammation and differentiation of immune cells. However, little is known about the role of Rab44 in inflammation. In this study, we showed that Rab44 was upregulated during the early phase of differentiation of M1- and M2-type macrophages. Rab44-deficient mice exhibited impaired tumor necrosis factor alpha and interleukin-10 production after lipopolysaccharide (LPS) stimulation. The number of granulocytes in Rab44-deficient mice was lower, but the lymphocyte count in Rab44-deficient mice was significantly higher than that in wild-type mice after LPS stimulation. Moreover, Rab44-deficient macrophages showed impaired nickel-induced toxicity, and Rab44-deficient mice showed impaired nickel-induced hypersensitivity. Upon nickel hypersensitivity induction, Rab44-deficient mice showed different frequencies of immune cells in the blood and ears. Thus, it is likely that Rab44 is implicated in immune cell differentiation and inflammation, and Rab44 deficiency induces impaired immune responses to nickel allergies.


Subject(s)
Hypersensitivity , Nickel , Mice , Animals , Nickel/toxicity , Lipopolysaccharides/toxicity , Hypersensitivity/genetics , rab GTP-Binding Proteins/genetics , rab GTP-Binding Proteins/metabolism , Inflammation , Immunity
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