Blood–spinal cord barrier pericyte reductions contribute to increased capillary permeability

EA Winkler, JD Sengillo, RD Bell… - Journal of Cerebral …, 2012 - journals.sagepub.com
EA Winkler, JD Sengillo, RD Bell, J Wang, BV Zlokovic
Journal of Cerebral Blood Flow & Metabolism, 2012journals.sagepub.com
The blood–spinal cord barrier (BSCB) regulates molecular exchange between blood and
spinal cord. Pericytes are presumed to be important cellular constituents of the BSCB.
However, the regional abundance and vascular functions of spinal cord pericytes have yet to
be determined. Utilizing wild-type mice, we show that spinal cord pericyte capillary coverage
and number compared with the brain regions are reduced most prominently in the anterior
horn. Regional pericyte variations are highly correlated with:(1) increased capillary …
The blood–spinal cord barrier (BSCB) regulates molecular exchange between blood and spinal cord. Pericytes are presumed to be important cellular constituents of the BSCB. However, the regional abundance and vascular functions of spinal cord pericytes have yet to be determined. Utilizing wild-type mice, we show that spinal cord pericyte capillary coverage and number compared with the brain regions are reduced most prominently in the anterior horn. Regional pericyte variations are highly correlated with: (1) increased capillary permeability to 350 Da, 40,000 Da, and 150,000 Da, but not 2,000,000 Da fluorescent vascular tracers in cervical, thoracic, and lumbar regions and (2) diminished endothelial zonula occludens-1 (ZO-1) and occludin tight junction protein expression. Pericyte-deficient mutations (PdgfrβF7/F7 mice) resulted in additional pericyte reductions in spinal cord capillaries leading to overt BSCB disruption to serum proteins, accumulation in motor neurons of cyotoxic thrombin and fibrin and motor neuron loss. Barrier disruption in perciyte-deficient mice coincided with further reductions in ZO-1 and occludin. These data suggest that pericytes contribute to proper function of the BSCB at the capillary level. Regional reductions in spinal cord pericytes may provide a cellular basis for heightened spinal cord barrier capillary permeability and motor neuron loss.
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