85 The main scar-forming cells in the CNS are perivascular fibroblasts 89 and type A pericytes, 90 which produce the fibrotic extracellular matrix that cements the scar
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Tau has been shown to reduce secondary brain injury after CI by down-regulating the expression of matrix metalloproteinases-3 (MMP-3) in brain-injured rats, thereby protecting the BBB ( Furthermore, investigation revealed that BC and its active constituents, including Tau, TUDCA, and UDCA, can decrease lactate dehydrogenase levels, increase -GT content, raise TEER values, and decrease fluorescein sodium permeability coefficient
However, this proliferation was not observed in older cells