# Core C Cell and Tissue Imaging and Analysis

> **NIH NIH P01** · BRIGHAM AND WOMEN'S HOSPITAL · 2022 · $256,283

## Abstract

SUMMARY
This Cell and Tissue Imaging and Analysis Core seeks provides a centralized and integrated resource for in situ
proteomic analysis and imaging of the cellular and antigenic bioarchitecture of skin stem cells as a function of
chronologic age and in the context of age-related deficiency in wound healing. It also provides translational
validation through comparative examination of experimental murine and human skin selected as matched pairs
by expert dermatopathologists to ensure cross-relevance. The Core thus combines highly skilled professional
dermatopathology analysis and cutting-edge multiplex imaging technologies that permit sequential assessment
of how cells and molecules behave in healing wounds, and how this behavior is compromised in the setting of
age-related skin stem cell depletion/dysfunction. Specific Aim 1 provides PPG investigators with conventional
histology of formalin-fixed, paraffin-embedded (FFPE) biospecimens, multiplex labeling for 3-4 epitopes, image
quantification, and a variety of optional specialized technologies on an as-needed basis. This aim is essential to
assess the cellular constituents and efficiency of wound healing responses in the context of various experimental
models proposed in Projects 1-3 and in a manner that permits comparisons across projects. It also provides key
data that will interface with the Bioinformatics Core (Core B), and assists in developing strategies to enhance
wound healing through understanding potential utility of targeted therapeutic approaches directed at defective
stem cell-driven repair pathways. Importantly, it offers standardized and uniform expertise and experience not
available through simultaneous use of multiple institutional pathology resources. Specific Aim 2 takes multiplex
labeling to the level of high-resolution, highly-plexed imaging, whereby cellular and proteomic intricacies can for
the first time be visually unraveled at the level of 20 or more simultaneously identifiable antibody probes. This
approach leverages in-house technology involving NanoZoomer scanning technology and QuPath data analysis
in order to provide state-of-the art quantitative and spatial analysis of multiple epitopes expressed in situ by cells
and their microenvironments relevant to skin aging and stem cell involvement in the wound healing process. It
is fortified by collaborative interactions with Dr. Peter Sorger and application of related CyCIF labeling
technology, as well as the availability of GeoMx technology for digital spatial proteomic and genomic profiling.
Aim 3 provides an extensive human skin biobank whereby data generated by Core analyses of murine models
may be readily compared and contrasted with relevant age-matched and co-morbidity-controlled wound healing
responses in the human integument, as well as accessing and prospectively accumulating a wealth of relevant
biospecimens for PPG analyses. Core C thus provides an essential, centralized, and highly integrated analytical
com...

## Key facts

- **NIH application ID:** 10494657
- **Project number:** 1P01AG071463-01A1
- **Recipient organization:** BRIGHAM AND WOMEN'S HOSPITAL
- **Principal Investigator:** GEORGE F MURPHY
- **Activity code:** P01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2022
- **Award amount:** $256,283
- **Award type:** 1
- **Project period:** 2022-09-30 → 2027-05-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10494657

## Citation

> US National Institutes of Health, RePORTER application 10494657, Core C Cell and Tissue Imaging and Analysis (1P01AG071463-01A1). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10494657. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*
