Early changes of LIFR and gp130 in sciatic nerve and muscle of diabetic mice |
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Authors: | Toledo-Corral Claudia M Banner Lisa R |
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Affiliation: | Department of Biology, California State University, Northridge, 18111 Nordhoff St., Northridge, CA 91330-8330, USA |
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Abstract: | Peripheral neuropathy is a common complication of diabetes mediated by alterations of growth factors. Members of the neuropoietic cytokine family, which include IL-6, LIF, and CNTF among others, have been shown to be important regulators of peripheral nerves and the muscles that they innervate. To investigate their potential role in diabetic nerve and muscle, we studied the expression of the shared receptor subunits, LIFR and gp130 in a mouse model of streptozotocin (STZ)-induced diabetes. The results of Western blotting and densitometric analysis showed that both LIFR and gp130 protein expression were increased in diabetic sciatic nerve compared to control mice at early time points following STZ injection. In diabetic gastrocnemius muscle, LIFR and gp130 were increased from 3 days to 24 weeks following STZ injection. In contrast, both LIFR and gp130 protein expression were decreased in diabetic soleus muscle at 3-days post-injection. Our results suggest that hyperglycemia results in changes to nerve and muscle soon after the onset of diabetes and that cytokines may play a role in this process. |
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Keywords: | BDNF, brain-derived neurotrophic factor CT-1, cardiotropin-1 CLC, cardiotrophin-like cytokine CIDP, chronic inflammatory demyelinating polyneuropathy CNTF, ciliary neurotrophic factor GDNF, glial cell-line derived neurotrophic factor IGF, insulin-like growth factor IL-1, interleukin-1 IL-6, interleukin-6 IL-11, interleukin-11 IL-1RA, IL-1 receptor antagonist LIF, leukemia inhibitory factor NGF, nerve growth factor NT-3, neurotrophin-3 NT-4, neurotrophin-4 OSM, oncostatin-M STZ, streptozotocin VEGF, vascular endothelial growth factor |
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