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2.
J Neurosci ; 32(10): 3296-300, 2012 Mar 07.
Artículo en Inglés | MEDLINE | ID: mdl-22399751

RESUMEN

The cutaneous somatosensory system contains multiple types of mechanoreceptors that detect different mechanical stimuli (Johnson, 2001). These stimuli, either alone or in combination, are ultimately interpreted by the brain as different aspects of the sense of touch. Psychophysical and electrophysiological experiments in humans and other mammals implicate one of these mechanoreceptors, the Merkel cell/neurite complex, in two-point discrimination and the detection of curvature, shape, and texture (Johnson and Lamb, 1981; Johnson et al., 2000; Johnson, 2001). However, whether Merkel cell/neurite complex function is required for the detection of these stimuli is unknown. We genetically engineered mice that lack Merkel cells (Maricich et al., 2009; Morrison et al., 2009) to directly test the hypothesis that Merkel cell/neurite complexes are necessary to perform these types of sensory discrimination tasks. We found that mice devoid of Merkel cells could not detect textured surfaces with their feet while other measures of motor and sensory function were unaffected. Interestingly, these mice retained the ability to discriminate both texture and shape using their whiskers, suggesting that other somatosensory afferents can functionally substitute for Merkel cell/neurite complexes in this sensory organ. These findings suggest that Merkel cell/neurite complexes are essential for texture discrimination tasks involving glabrous skin but not whiskers.


Asunto(s)
Discriminación en Psicología/fisiología , Células de Merkel/fisiología , Desempeño Psicomotor/fisiología , Tacto/fisiología , Animales , Femenino , Masculino , Ratones , Ratones Noqueados , Ratones Transgénicos , Neuritas/fisiología , Vibrisas/fisiología
3.
Physiol Plant ; 140(4): 334-41, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-20738805

RESUMEN

Environmental factors, such as ultraviolet-B (UV-B) irradiation, have the ability to affect pathways such as nitrogen metabolism. As fixed nitrogen is the keystone mineral nutrient that controls grain crop yield, any alteration in this cycle can be detrimental to plant productivity. Nitrate reductase enzyme activity is responsible for the reduction of nitrate to nitrite, and nitrate is the major form of nitrogen assimilated in plants. In maize (Zea mays L.) production, nitrate assimilation kinetics are important for both high- and low-input agricultural systems. Nitrate reductase protein activity is controlled by phosphatases and kinases. Nitrate reductase activity is responsive to environmental signals such as light-dark cycles and UV-B radiation, although the regulatory controls are not yet fully understood. We have determined the location of maize genetic factors that control nitrate reductase activity and the extent of contribution of each of these factors, both locally in the leaf tissue and via long-distance signaling loci that affect root nitrate reductase activity upon leaf UV irradiation. In the IBM94 recombinant inbred mapping population, the loci controlling regulation of nitrate reductase activity under UV-B map to different positions than the loci controlling nitrate reductase activity in unexposed plants.


Asunto(s)
Alelos , Nitrato-Reductasa/genética , Hojas de la Planta/enzimología , Raíces de Plantas/enzimología , Sitios de Carácter Cuantitativo/genética , Rayos Ultravioleta , Zea mays/enzimología , Ambiente , Regulación de la Expresión Génica de las Plantas/efectos de la radiación , Hojas de la Planta/genética , Hojas de la Planta/efectos de la radiación , Raíces de Plantas/genética , Raíces de Plantas/efectos de la radiación , Transducción de Señal/genética , Transducción de Señal/efectos de la radiación , Zea mays/genética , Zea mays/efectos de la radiación
4.
Dev Biol ; 336(1): 76-83, 2009 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-19782676

RESUMEN

Merkel cells are specialized cells in the skin that are important for proper neural encoding of light touch stimuli. Conflicting evidence suggests that these cells are lineally descended from either the skin or the neural crest. To address this question, we used epidermal (Krt14(Cre)) and neural crest (Wnt1(Cre)) Cre-driver lines to conditionally delete Atoh1 specifically from the skin or neural crest lineages, respectively, of mice. Deletion of Atoh1 from the skin lineage resulted in loss of Merkel cells from all regions of the skin, while deletion from the neural crest lineage had no effect on this cell population. Thus, mammalian Merkel cells are derived from the skin lineage.


Asunto(s)
Linaje de la Célula , Células Epidérmicas , Células de Merkel/citología , Animales , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/genética , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/metabolismo , Embrión de Mamíferos/citología , Embrión de Mamíferos/embriología , Embrión de Mamíferos/metabolismo , Epidermis/embriología , Epidermis/metabolismo , Femenino , Inmunohistoquímica , Queratina-14/genética , Queratina-14/metabolismo , Masculino , Células de Merkel/metabolismo , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Sistema Nervioso/citología , Sistema Nervioso/embriología , Sistema Nervioso/metabolismo , Piel/citología , Piel/embriología , Piel/metabolismo , Factores de Tiempo , Proteína Wnt1/genética , Proteína Wnt1/metabolismo
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