To explore the neural mechanisms mediating agingrelated visual function declines, we compared the expressions of brain-derived neurotrophic factor（BDNF） and its high affinity receptor-tyrosine kinase B（Trk B） betw...To explore the neural mechanisms mediating agingrelated visual function declines, we compared the expressions of brain-derived neurotrophic factor（BDNF） and its high affinity receptor-tyrosine kinase B（Trk B） between young and old adult cats. Nissl staining was used to display neurons in each layer of the lateral geniculate nucleus（LGN）. The BDNF- and Trk B receptor-immunoreactive neurons were labeled immunohistochemically, observed under optical microscope and photographed. Their neuronal density and immunoreactive intensity were measured. Results showed that the mean density of the Nissl stained neurons in each LGN layer were comparable between old and young adult cats, and their BDNF and Trk B proteins were widely expressed in all LGN layers. However, compared with young adult cats, both the density and optical absorbance intensity of BDNF- and Trk B-immunoreactive cells in each LGN layer in old cats were significantly decreased. These findings indicate that the decreased expressions of BDNF and Trk B proteins in the LGN may be an important factor inducing the compromised inhibition in the central visual nucleus and the functional visual decline in senescent individuals.展开更多
Restorative cell-based therapies for experimental brain injury, such as stroke and traumatic brain injury,substantially improve functional outcome. We discuss and review state of the art magnetic resonance imaging met...Restorative cell-based therapies for experimental brain injury, such as stroke and traumatic brain injury,substantially improve functional outcome. We discuss and review state of the art magnetic resonance imaging methodologies and their applications related to cell-based treatment after brain injury. We focus on the potential of magnetic resonance imaging technique and its associated challenges to obtain useful new information related to cell migration, distribution, and quantitation, as well as vascular and neuronal remodeling in response to cell-based therapy after brain injury. The noninvasive nature of imaging might more readily help with translation of cell-based therapy from the laboratory to the clinic.展开更多
基金This study was supported by the National Natural Science Foundation of China （31171082） the Key Project of Natural Science Research of the Education Bureau of Anhui Province （KJ2014A284） the Foundation of Key Laboratories of Anhui Province and Key Laboratories of Universities of Anhui Province
文摘To explore the neural mechanisms mediating agingrelated visual function declines, we compared the expressions of brain-derived neurotrophic factor（BDNF） and its high affinity receptor-tyrosine kinase B（Trk B） between young and old adult cats. Nissl staining was used to display neurons in each layer of the lateral geniculate nucleus（LGN）. The BDNF- and Trk B receptor-immunoreactive neurons were labeled immunohistochemically, observed under optical microscope and photographed. Their neuronal density and immunoreactive intensity were measured. Results showed that the mean density of the Nissl stained neurons in each LGN layer were comparable between old and young adult cats, and their BDNF and Trk B proteins were widely expressed in all LGN layers. However, compared with young adult cats, both the density and optical absorbance intensity of BDNF- and Trk B-immunoreactive cells in each LGN layer in old cats were significantly decreased. These findings indicate that the decreased expressions of BDNF and Trk B proteins in the LGN may be an important factor inducing the compromised inhibition in the central visual nucleus and the functional visual decline in senescent individuals.
基金supported by NIH grants RO1 NS64134 and RO1 NS 48349
文摘Restorative cell-based therapies for experimental brain injury, such as stroke and traumatic brain injury,substantially improve functional outcome. We discuss and review state of the art magnetic resonance imaging methodologies and their applications related to cell-based treatment after brain injury. We focus on the potential of magnetic resonance imaging technique and its associated challenges to obtain useful new information related to cell migration, distribution, and quantitation, as well as vascular and neuronal remodeling in response to cell-based therapy after brain injury. The noninvasive nature of imaging might more readily help with translation of cell-based therapy from the laboratory to the clinic.
