4.5 Article

Pericyte structure and distribution in the cerebral cortex revealed by high-resolution imaging of transgenic mice

Journal

NEUROPHOTONICS
Volume 2, Issue 4, Pages -

Publisher

SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS
DOI: 10.1117/1.NPh.2.4.041402

Keywords

microcirculation; capillary; cerebral blood blow; two-photon microscopy; pericyte; smooth muscle

Funding

  1. NCATS NIH HHS [UL1 TR000062] Funding Source: Medline
  2. NCI NIH HHS [P30 CA138313] Funding Source: Medline
  3. NIGMS NIH HHS [P30 GM103392, P20 GM109040, T32 GM008716] Funding Source: Medline
  4. NINDS NIH HHS [R21 NS096997, R21 NS085402] Funding Source: Medline

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Pericytes are essential for normal brain function, but many aspects of their physiology remain enigmatic due to a lack of tools to genetically target this cell population. Here, we characterize brain pericytes using two existing Cre-recombinase driver mouse lines that can serve distinct purposes in cerebrovascular research. One line expresses an inducible version of Cre under the NG2 proteoglycan promoter, which provides the sparse labeling necessary to define the morphology of single cells. These mice reveal structural differences between pericytes adjacent to arterioles versus those broadly distributed in the capillary bed that may underlie differential roles in control of vessel caliber. A second line expresses Cre constitutively under the platelet-derived growth factor receptor beta promoter and provides continuous, highly specific and near-complete labeling of pericytes and myocytes along the entire cerebrovasculature. This line provides a three-dimensional view of pericyte distribution along the cortical angioarchitecture following optical clearing of brain tissue. In combination with recent reporter lines for expression of optogenetic actuators and activity-sensitive probes, these mice may be key tools for studying pericyte biology in the intact brain. (C) 2015 Society of Photo-Optical Instrumentation Engineers (SPIE)

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