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2.
Nutrients ; 9(8)2017 Aug 04.
Artigo em Inglês | MEDLINE | ID: mdl-28777295

RESUMO

Estrogens play a key role in an extensive range of physiological functions in various types of tissues throughout the body in females. We previously showed that estrogen insufficiency caused muscle weakness that could be rescued by estrogen administration in a young female ovariectomized (OVX) mouse model. However, long-term estrogen replacement therapy increases risks of breast cancer and cardiovascular diseases. Soymilk contains plant-based protein and isoflavones that exert estrogen-like activity. Here we examined the effects of prolonged soymilk intake on muscle and its resident stem cells, called satellite cells, in the estrogen-insufficient model. Six-week-old C57BL/6 OVX female mice were fed with a dried soymilk-containing diet. We found that prolonged soymilk intake upregulated grip strength in OVX mice. Correspondingly, cross-sectional area of tibialis anterior muscle was significantly increased in OVX mice fed with soymilk. Furthermore, soymilk diet mitigated dysfunction of satellite cells isolated from OVX mice. Thus, these results indicated that prolonged soymilk intake is beneficial for improving muscle weakness in an estrogen-insufficient state in females.


Assuntos
Estrogênios/deficiência , Força Muscular , Debilidade Muscular/dietoterapia , Músculo Esquelético/fisiopatologia , Ovariectomia , Leite de Soja/administração & dosagem , Fatores Etários , Ração Animal , Animais , Células Cultivadas , Modelos Animais de Doenças , Feminino , Força da Mão , Camundongos Endogâmicos C57BL , Debilidade Muscular/metabolismo , Debilidade Muscular/patologia , Debilidade Muscular/fisiopatologia , Músculo Esquelético/metabolismo , Músculo Esquelético/patologia , Células Satélites de Músculo Esquelético/metabolismo , Células Satélites de Músculo Esquelético/patologia , Fatores de Tempo
3.
J Dermatol ; 43(11): 1336-1339, 2016 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-27334898

RESUMO

Merkel cell carcinoma (MCC) is a rare but aggressive cutaneous malignancy associated with the Merkel cell polyomavirus (MCPyV). Multiple studies have shown that the incidence of MCC is higher among immunocompromised individuals than among the general population. In fact, immunosuppressed individuals account for approximately 10% of the MCC patient population. In this report, we describe two cases of MCPyV-related MCC in Japanese patients on hemodialysis. In both the cases, MCC was present on the face. Both cellular and humoral immunities have been shown to be decreased in uremic patients, and dialysis patients have a high risk of viral-mediated cancers, including human papillomavirus-associated cancers. Immune dysfunction related to uremia and dialysis may be associated with a high risk of developing MCC.


Assuntos
Carcinoma de Célula de Merkel/etiologia , Neoplasias Cutâneas/etiologia , Uremia/complicações , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Diálise Renal/efeitos adversos , Uremia/terapia
4.
Methods Mol Biol ; 1516: 183-193, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27052612

RESUMO

Skeletal muscle stem cells are satellite cells that play crucial roles in tissue repair and regeneration after muscle injury. Accumulating evidence indicates that satellite cells are genetically and functionally heterogeneous, even within the same muscle. A small population of satellite cells possesses "stemness" and exhibits the remarkable ability to regenerate through robust self-renewal when transplanted into a regenerating muscle niche. In contrast, not all satellite cells self-renew. For example, some cells are committed myogenic progenitors that immediately undergo myogenic differentiation with minimal cell division after activation. Recent studies illuminate the cellular and molecular characteristics of the functional heterogeneity among satellite cells. To evaluate heterogeneity and stem cell dynamics, here we describe methods to conduct a clonal analysis of satellite cells and to visualize a slowly dividing cell population.


Assuntos
Rastreamento de Células/métodos , Células Satélites de Músculo Esquelético/citologia , Análise de Célula Única/métodos , Células-Tronco/citologia , Animais , Diferenciação Celular/genética , Proliferação de Células/genética , Heterogeneidade Genética , Camundongos , Desenvolvimento Muscular/genética
5.
FASEB J ; 30(5): 1733-40, 2016 05.
Artigo em Inglês | MEDLINE | ID: mdl-26718889

RESUMO

µ-Crystallin (Crym), a thyroid hormone-binding protein, is abnormally up-regulated in the muscles of patients with facioscapulohumeral muscular dystrophy, a dominantly inherited progressive myopathy. However, the physiologic function of Crym in skeletal muscle remains to be elucidated. In this study, Crym was preferentially expressed in skeletal muscle throughout the body. Crym-knockout mice exhibited a significant hypertrophy of fast-twitch glycolytic type IIb fibers, causing an increase in grip strength and high intensity running ability in Crym-null mice. Genetic inactivation of Crym or blockade of Crym by siRNA-mediated knockdown up-regulated the gene expression of fast-glycolytic contractile fibers in satellite cell-derived myotubes in vitro These alterations in Crym-inactivated muscle were rescued by inhibition of thyroid hormone, even though Crym is a positive regulator of thyroid hormone action in nonmuscle cells. The results demonstrated that Crym is a crucial regulator of muscle plasticity, controlling metabolic and contractile properties of myofibers, and thus the selective inactivation of Crym may be a potential therapeutic target for muscle-wasting diseases, such as muscular dystrophies and age-related sarcopenia.-Seko, D., Ogawa, S., Li, T.-S., Taimura, A., Ono, Y. µ-Crystallin controls muscle function through thyroid hormone action.


Assuntos
Cristalinas/metabolismo , Músculo Esquelético/fisiologia , Células Satélites de Músculo Esquelético/fisiologia , Tiroxina/metabolismo , Tri-Iodotironina/metabolismo , Animais , Antitireóideos , Cristalinas/genética , Camundongos , Camundongos Knockout , Interferência de RNA , RNA Interferente Pequeno , Tiroxina/genética , Tri-Iodotironina/genética , Regulação para Cima , Cristalinas mu
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