The glutamate/aspartate transporter GLAST-1 is expressed in bone in vivo and also exists as a splice variant (GLAST-1a) in which exon 3 is excluded. Since GLAST-1 expression is regulated in bone in response to osteogenic mechanical stimuli in vivo and binding of glutamate to receptors on osteoblasts increases osteoblast number and activity in vitro, control of extracellular glutamate concentrations may be critical for balanced bone remodelling. To determine whether GLAST isoforms may act to regulate extracellular glutamate concentration in bone we investigated whether their pattern or level of expression is responsive to glutamate concentration in bone cells. GLAST-1a mRNA is expressed at lower levels than GLAST-1 mRNA in all cells examined...
Osteoclasts are involved in the catabolism of the bone matrix and eliminate the resulting degradatio...
Bone relies on multiple extracellular signalling systems to maintain homeostasis of its normal struc...
The cellular mechanisms coupling mechanical loading with bone remodeling remain unclear. In the CNS,...
The glutamate/aspartate transporter GLAST-1 is expressed in bone in vivo and also exists as a splice...
In the central nervous system Na+-dependent glutamate transporters bind extracellular glutamate and ...
Without habitual exercise, bone is lost from the skeleton. Interactions between the effects of loadi...
The amino acid L-glutamate mediates signals at excitatory synapses in the CNS where its effects are ...
AbstractPreviously we have reported expression of an mRNA with homology to the Na+-dependent glutama...
Mechanical loading plays a key role in the physiology of bone, allowing bone to functionally adapt t...
Development and function of osteoblast lineage cells are regulated by a complex microenvironment con...
Mechanical loading of the skeleton is important for maintenance of adequate bone mass and defined me...
Previously we have reported expression of an mRNA with homology to the Na+-dependent glutamate trans...
Mechanical loading plays a key role in the physiology of bone, allowing bone to functionally adapt t...
Osteoclasts are involved in the catabolism of the bone matrix and eliminate the resulting degradatio...
Bone relies on multiple extracellular signalling systems to maintain homeostasis of its normal struc...
The cellular mechanisms coupling mechanical loading with bone remodeling remain unclear. In the CNS,...
The glutamate/aspartate transporter GLAST-1 is expressed in bone in vivo and also exists as a splice...
In the central nervous system Na+-dependent glutamate transporters bind extracellular glutamate and ...
Without habitual exercise, bone is lost from the skeleton. Interactions between the effects of loadi...
The amino acid L-glutamate mediates signals at excitatory synapses in the CNS where its effects are ...
AbstractPreviously we have reported expression of an mRNA with homology to the Na+-dependent glutama...
Mechanical loading plays a key role in the physiology of bone, allowing bone to functionally adapt t...
Development and function of osteoblast lineage cells are regulated by a complex microenvironment con...
Mechanical loading of the skeleton is important for maintenance of adequate bone mass and defined me...
Previously we have reported expression of an mRNA with homology to the Na+-dependent glutamate trans...
Mechanical loading plays a key role in the physiology of bone, allowing bone to functionally adapt t...
Osteoclasts are involved in the catabolism of the bone matrix and eliminate the resulting degradatio...
Bone relies on multiple extracellular signalling systems to maintain homeostasis of its normal struc...
The cellular mechanisms coupling mechanical loading with bone remodeling remain unclear. In the CNS,...