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2.
Nutrients ; 9(8)2017 Aug 04.
Artículo en Inglés | MEDLINE | ID: mdl-28777295

RESUMEN

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.


Asunto(s)
Estrógenos/deficiencia , Fuerza Muscular , Debilidad Muscular/dietoterapia , Músculo Esquelético/fisiopatología , Ovariectomía , Leche de Soja/administración & dosificación , Factores de Edad , Alimentación Animal , Animales , Células Cultivadas , Modelos Animales de Enfermedad , Femenino , Fuerza de la Mano , Ratones Endogámicos C57BL , Debilidad Muscular/metabolismo , Debilidad Muscular/patología , Debilidad Muscular/fisiopatología , Músculo Esquelético/metabolismo , Músculo Esquelético/patología , Células Satélite del Músculo Esquelético/metabolismo , Células Satélite del Músculo Esquelético/patología , Factores de Tiempo
3.
J Dermatol ; 43(11): 1336-1339, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27334898

RESUMEN

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.


Asunto(s)
Carcinoma de Células de Merkel/etiología , Neoplasias Cutáneas/etiología , Uremia/complicaciones , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Diálisis Renal/efectos adversos , Uremia/terapia
4.
Methods Mol Biol ; 1516: 183-193, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27052612

RESUMEN

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.


Asunto(s)
Rastreo Celular/métodos , Células Satélite del Músculo Esquelético/citología , Análisis de la Célula Individual/métodos , Células Madre/citología , Animales , Diferenciación Celular/genética , Proliferación Celular/genética , Heterogeneidad Genética , Ratones , Desarrollo de Músculos/genética
5.
FASEB J ; 30(5): 1733-40, 2016 05.
Artículo en Inglés | MEDLINE | ID: mdl-26718889

RESUMEN

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.


Asunto(s)
Cristalinas/metabolismo , Músculo Esquelético/fisiología , Células Satélite del Músculo Esquelético/fisiología , Tiroxina/metabolismo , Triyodotironina/metabolismo , Animales , Antitiroideos , Cristalinas/genética , Ratones , Ratones Noqueados , Interferencia de ARN , ARN Interferente Pequeño , Tiroxina/genética , Triyodotironina/genética , Regulación hacia Arriba , Cristalinas mu
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