期刊
NEUROMUSCULAR DISORDERS
卷 22, 期 5, 页码 435-442出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.nmd.2011.10.021
关键词
Microcirculation; Microvascular; Motor neurone disease; Capillaries; Spinal muscular atrophy
资金
- Newlife Foundation
- Euan MacDonald Centre for Motor Neurone Disease Research
- SMA Trust
- Biotechnology and Biological Sciences Research Council [BBS/E/D/20251969] Funding Source: researchfish
- BBSRC [BBS/E/D/20251969] Funding Source: UKRI
Spinal muscular atrophy (SMA) is traditionally described and characterised as a disease of the neuromuscular system. Recently, the vascular system has been implicated in SMA pathogenesis, but there are no reports on whether this impacts on skeletal muscle microvasculature. Using an established mouse model of severe SMA (Smn(-/-);SMN2(+/+)), we examined the capillary bed in three different skeletal muscles using quantitative imaging and western blotting in late symptomatic mice (P5). We found a dramatic (45%) decrease in the density of the capillary bed in all muscles examined compared to littermate controls at early and late symptomatic time points, and reduced expression of a key endothelial protein, PECAM-1. In addition, capillary calibre was increased by 50% in SMA mice while ramification of capillaries into muscle was reduced. Investigation of earlier developmental time points revealed identical changes at an early symptomatic time point (P3), but significantly, no difference at a pre-symptomatic time point (P1). These changes are likely to have considerable impact on the ability of the muscle capillary bed to deliver oxygen and remove metabolites from muscle and may therefore contribute to pathogenesis in SMA. (C) 2011 Elsevier B.V. All rights reserved.
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