# Investigation on ABCC6-Deficient Human Hepatocytes Generated by CRISPR–Cas9 Genome Editing

**Authors:** Ricarda Plümers, Svenja Jelinek, Christopher Lindenkamp, Michel R. Osterhage, Cornelius Knabbe, Doris Hendig

PMC · DOI: 10.3390/cells14080576 · Cells · 2025-04-11

## TL;DR

Scientists created liver cells with a genetic mutation linked to a rare disease called pseudoxanthoma elasticum to study its metabolic causes.

## Contribution

A novel in vitro model of ABCC6-deficient human hepatocytes was developed using CRISPR-Cas9 for studying pseudoxanthoma elasticum.

## Key findings

- ABCC6-deficient HepIms showed impaired lipid trafficking and extracellular matrix remodeling.
- Calcification inhibitor expression was induced in ABCC6-deficient cells.
- Senescence and inflammatory markers were downregulated in the ABCC6-deficient clones.

## Abstract

Patients affected by the rare disease pseudoxanthoma elasticum (PXE) exhibit the calcification of elastic fibers in ocular, dermal, and vascular tissues. These symptoms are triggered by mutations in the ATP-binding cassette transporter subfamily C member 6 (ABCC6), whose substrate remains unknown. Interestingly, ABCC6 is predominantly expressed in the liver tissue, leading to the hypothesis that PXE is a metabolic disorder. We developed a genome-editing system targeting ABCC6 in human immortalized hepatocytes (HepIms) for further investigations. The HepIms were transfected with an ABCC6-specific clustered regulatory interspaced short palindromic repeat (CRISPR-Cas9) genome-editing plasmid, resulting in the identification of a heterozygous (htABCC6HepIm) and a compound heterozygous (chtABCC6HepIm) clone. These clones were analyzed for key markers associated with the PXE pathobiochemistry. Hints of impaired lipid trafficking, defects in the extracellular matrix remodeling, the induction of calcification inhibitor expression, and the down regulation of senescence and inflammatory markers in ABCC6-deficienct HepIms were found. Our ABCC6 knock-out model of HepIms provides a valuable tool for studying the metabolic characteristics of PXE in vitro. The initial analysis of the clones mirrors various features of the PXE pathobiochemistry and provides an outlook on future research approaches.

## Linked entities

- **Genes:** ABCC6 (ATP binding cassette subfamily C member 6) [NCBI Gene 368]
- **Diseases:** pseudoxanthoma elasticum (MONDO:0009925)

## Full-text entities

- **Genes:** ABCC6 (ATP binding cassette subfamily C member 6) [NCBI Gene 368] {aka ABC34, ARA, EST349056, GACI2, MLP1, MOAT-E}
- **Diseases:** inflammatory (MESH:D007249), calcification (MESH:D002114), PXE (MESH:D011561), metabolic disorder (MESH:D008659)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12025709/full.md

## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12025709/full.md

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Source: https://tomesphere.com/paper/PMC12025709