| Literature DB >> 26695138 |
Hiroshi Urabe1, Tomoya Terashima2, Hideto Kojima3, Lawrence Chan4.
Abstract
Diabetic peripheral neuropathy (DPN) is a major diabetic complication. Previously, we showed that hyperglycemia induces the appearance of proinsulin (PI)-producing bone marrow-derived cells (PI-BMDCs), which fuse with dorsal root ganglion neurons, causing apoptosis, nerve dysfunction, and DPN. In this study, we have devised a strategy to ablate PI-BMDCs in mice in vivo. The use of this strategy to selectively ablate TNFα-producing PI-BMDCs in diabetic mice protected these animals from developing DPN. The findings provide powerful validation for a pathogenic role of PI-BMDCs and identify PI-BMDCs as an accessible therapeutic target for the treatment and prevention of DPN.Entities:
Keywords: bone marrow-derived cells; diabetic peripheral neuropathy; diphtheria toxin; diphtheria toxin receptor; dorsal root ganglion; proinsulin; tumor necrosis factor-α
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Year: 2015 PMID: 26695138 PMCID: PMC4971812 DOI: 10.1152/ajpendo.00381.2015
Source DB: PubMed Journal: Am J Physiol Endocrinol Metab ISSN: 0193-1849 Impact factor: 4.310