# Role of Endo180 Regulation in Tissue Fibrosis

> **NIH NIH K08** · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · 2020 · $172,098

## Abstract

PROJECT SUMMARY
Title: Role of Endo180 Regulation in Tissue Fibrosis.
Despite extensive research, the pathogenesis of tissue fibrosis is still incompletely understood. This is
particularly true of the resolution of tissue fibrosis. The cellular degradation and remodeling of collagen, the main
component of fibrotic tissue, has been proven important in regulating the severity of tissue fibrosis. Yet, the
regulatory mechanisms that control this process remain largely unknown. Endo180 is the canonical collagen
endocytic receptor. Genetic deletion of this receptor results in exaggerated fibrosis in experimental models in
the lung, liver and kidney. The control of Endo180, however, is mostly unstudied. Our laboratory previously
published an RNAi-based screen of Drosophila phagocytes that identified promising candidate genes that
regulate collagen uptake in cells. In preliminary data, I have shown that two candidate genes from this screen,
Myeloid Zinc Finger-1 (MZF1) and Cell division cycle-7 kinase (CDC7), regulate Endo180 expression. The
research proposed in this grant application seeks to define the mechanistic bases of regulation of Endo180 by
these two molecules, at the genetic and epigenetic levels. In addition, I propose to demonstrate the
consequences of interfering with these pathways in in vivo models of fibrosis. The proposed research is
significant because it is expected to advance our understanding of matrix biology and cell-matrix communication.
In addition, this research will identify promising new pathways that can be targeted therapeutically to augment
the resolution of fibrosis in human disease. This would represent a novel approach to treating fibrotic disease.
The training objectives and related research activities of this proposal will provide new skills, manuscripts and
pilot data related to fibrosis resolution and Endo180 regulation in mice and humans. This will be necessary to
establish my independence in these areas and obtain R01 funding to advance this unique research program.

## Key facts

- **NIH application ID:** 9989153
- **Project number:** 5K08HL145015-02
- **Recipient organization:** UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
- **Principal Investigator:** Michael Podolsky
- **Activity code:** K08 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $172,098
- **Award type:** 5
- **Project period:** 2019-08-15 → 2024-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9989153

## Citation

> US National Institutes of Health, RePORTER application 9989153, Role of Endo180 Regulation in Tissue Fibrosis (5K08HL145015-02). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/9989153. Licensed CC0.

---

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