Specific Aims

Goals of the proposed research

Cerebral blood flow impairments are implicated in the pathogenesis of myriad neurological diseases, from multiple sclerosis to dementia. Understanding how cerebral blood flow is regulated under normal conditions may thus permit the development of therapies that can correct blood flow abnormalities and thereby alter the trajectory of neurological diseases. Studies consistently reveal two broad categories of blood flow impairment: 1. abnormal perfusion (hypo- or hyperperfusion), and 2. dampened vasodynamics, defined as a reduced ability of the cerebrovasculature to rapidly change resistance to blood flow in response to environmental shifts such as neural activity, blood pressure, oxygen level, etc. The cells responsible for regulating perfusion and vasodynamics are vascular mural cells, comprised of vascular smooth muscle cells (VSMCs) and pericytes, which adorn the abluminal endothelium. While it is accepted that arterioles ensheathed by vascular smooth muscle cells (VSMCs) are capable of regulating blood flow by modulating vessel diameter, it is debated whether capillaries lined with pericytes can also regulate blood flow. The goal of this dissertation is to clarify the elements of the cerebrovasculature that can regulate blood flow under non-pathological conditions.

Hypothesis

Pericytes are by definition embedded in the capillary basement membrane, placing them in a perfect position to control capillary blood flow. However, in vivo investigations into the capacity of pericytes to regulate capillary blood flow provide opposing conclusions, placing the field in a stalemate. One study claims that pericytes on capillaries can regulate cerebral blood flow, whereas another concluded that VSMCs on arterioles can control blood flow, but pericytes on capillaries cannot. Adding to the uncertainty of which cerebrovascular elements regulate blood flow in vivo, these studies defined pericytes differently. Hall, et al. (2014) identified pericytes by the appearance of a protruberant ovoid cell body, a characteristic of pericytes, whereas Hill, et al. (2015) identified pericytes by the lack of alpha smooth muscle actin ( ( class="ltx_Math" contenteditable="false" data-equation="\alpha">\(\alpha\)SMA), a protein that confers contractile ability to VSMCs.These and other studies To advance the field beyond this stalemate, we aim to identify the vascular mural cells that (1) are capable of modulating vascular resistance, (2) participate in blood flow changes that occur during sensory-evoked hyperemia, and (3) express contractile proteins such as class="ltx_Math" contenteditable="false" data-equation="\alpha">\(\alpha\)SMA. Based on preliminaryin vivo data showing pericyte contractility constriction of the vascular lumen in regions of the vasculature that do not express class="ltx_Math" contenteditable="false" data-equation="\alpha">\(\alpha\)SMA, I hypothesize that capillary pericytes, even those without \(\alpha\)SMA, can regulate blood flow.

Explain flow.

Explain how the hypothesis is going to be tested. Aim 1: find out where pericyte and VSMC features co-exist. this should match where contractility ends

ends

class="ltx_title_subsection">Specific Aims

Specific Aim 3: Given the reported absence of aSMA in the higher order capillaries, what proteins could confer pericytes in the middle of the capillary bed contractile ability? Clearing is good because it maintains branch order and enables immunohistochemical labeling. However, there are proteins other than aSMA that enable vessels to constrict...Ira Hermann, D'Amore...peripheral tissues. Other components besides aSMA in contractile machinery. Myosin light chain kinase?? show aSMA in seeDB

Specific Aim 1: To examine the capacity of pericytes and VSMCs to regulate blood flow in lightly-anesthetized mice, we will use in vivo two photon microscopy to visualize and excite ChR2-YFP expressed specifically in vascular mural cells. Elaborate

Our breeding strategy crosses mice expressing Cre recombinase under the control of the promoter for platelet-derived growth factor receptor beta (PDGFRBeta-Cre) with mice that expresses ChR2-YFP only in cells that express Cre (Ai32). Because PDGFRBeta is highly expressed in vascular mural cells, the result of the cross is mice with optically-excitable ion channels selectively in vascular mural cells (henceforth called PDGFRBeta-ChR2 animals). In line with previous work, we have found that two photon imaging at an 800 nm laser wavelength produces marked constriction of arterioles expressing ChR2-YFP, thus indicating that one can simultaneously image YFP and excite ChR2. We will visualize and excite all components of the cerebrovasculature by measuring changes in lumenal diameter through a craniotomy using in vivo two photon microscopy.

Elaborate on "visualize and excite". Wavelengths used to image YFP can also be used to excite ChR2 cation influx. To control for non-specific light-induced changes (damage), we will perform the same studies using identical laser powers in animals expressing YFP without ChR2 in mural cells. prelim: show the in vivo data

Specific Aim 2: To test if pericytes and VSMCs control functional increases in blood flow, we will measure the effect of ChR2 excitation on blood flow velocity with and without vibrissae stimulation in chlorprothixene-anesthetized mice expressing ChR2-YFP in vascular mural cells.

expected outcomes and how they relate to hypothesis

hypothesis