# Loss of c-Kit in Endothelial Cells Protects against Hindlimb Ischemia

**Authors:** Gustavo Falero-Diaz, Catarina de A. Barboza, Roberto I. Vazquez-Padron, Omaida C. Velazquez, Roberta M. Lassance-Soares

PMC · DOI: 10.3390/biomedicines12061358 · 2024-06-19

## TL;DR

Removing c-Kit in blood vessel cells improves blood flow and protects against leg ischemia in mice.

## Contribution

This study reveals that endothelial c-Kit signaling negatively affects blood vessel formation and barrier integrity in ischemia.

## Key findings

- Mice lacking endothelial c-Kit or SCF showed improved limb perfusion and arteriogenesis.
- Endothelial barrier integrity was preserved in c-Kit and SCF knockout mice after aortic crush.
- Lower c-Kit and SCF gene expression was confirmed in endothelial cells of knockout mice.

## Abstract

Background: Critical limb ischemia (CLI) is the end stage of peripheral artery disease (PAD), and around 30% of CLI patients are ineligible for current treatments. The angiogenic benefits of c-Kit have been reported in the ischemia scenario; however, the present study demonstrates the effects of specific endothelial c-Kit signaling in arteriogenesis during hindlimb ischemia. Methods: We created conditional knockout mouse models that decrease c-Kit (c-Kit VE-Cadherin CreERT2—c-Kit) or its ligand (SCF VE-Cadherin CreERT2—SCF) specifically in endothelial cells (ECs) after tamoxifen treatment. These mice and a control group (wild-type VE-Cadherin CreERT2—WT) were subjected to hindlimb ischemia or aortic crush to evaluate perfusion/arteriogenesis and endothelial barrier permeability, respectively. Results: Our data confirmed the lower gene expression of c-Kit and SCF in the ECs of c-Kit and SCF mice, respectively. In addition, we confirmed the lower percentage of ECs positive for c-Kit in c-Kit mice. Further, we found that c-Kit and SCF mice had better limb perfusion and arteriogenesis compared to WT mice. We also demonstrated that c-Kit and SCF mice had a preserved endothelial barrier after aortic crush compared to WT. Conclusions: Our data demonstrate the deleterious effects of endothelial SCF/c-Kit signaling on arteriogenesis and endothelial barrier integrity.

## Linked entities

- **Genes:** KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815], KITLG (KIT ligand) [NCBI Gene 4254]
- **Chemicals:** tamoxifen (PubChem CID 2733526)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cdh5 (cadherin 5) [NCBI Gene 12562] {aka 7B4, Cd144, VE-Cad, VECD, VEcad, Vec}, Kit (Kit proto-oncogene receptor tyrosine kinase) [NCBI Gene 16590] {aka Bs, CD117, Fdc, Gsfsco1, Gsfsco5, Gsfsow3}, Kitl (kit ligand) [NCBI Gene 17311] {aka Clo, Con, Gb, Kitlg, Mgf, SCF}
- **Diseases:** CLI (MESH:D000089802), crush (MESH:D003444), PAD (MESH:D058729), Hindlimb Ischemia (MESH:D007511)
- **Chemicals:** tamoxifen (MESH:D013629)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11201387/full.md

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Source: https://tomesphere.com/paper/PMC11201387