Generation of spCAS9 expressing human mesenchymal stem cell line to study gene function during osteoblast differentiation.

Ines Foessl; Yuan Guo; Rosinda Mies; Moustapha Kassem; Johannes P T M van Leeuwen; Bram C J van der Eerden; Barbara Obermayer-Pietsch; Jeroen van de Peppel

doi:10.1093/jbmrpl/ziag117

PubMed · 42688902

Generation of spCAS9 expressing human mesenchymal stem cell line to study gene function during osteoblast differentiation.

Ines Foessl·Yuan Guo·Rosinda Mies·Moustapha Kassem·Johannes P T M van Leeuwen·Bram C J van der Eerden·Barbara Obermayer-Pietsch·Jeroen van de Peppel

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Abstract

Human bone marrow-derived stromal cells (hMSCs) are a great resource for studying how genes influence cell fate and differentiation into various cell types like osteoblasts, adipocytes, and chondrocytes, among other cell types. However, genetic manipulation of primary hMSCs has been challenging due to their short lifespan and cellular senescence after limited passaging. Their low and unstable transfection efficiency also complicates gene delivery or inactivation, hindering long-term functional studies. The limited lifespan has been effectively solved by immortalizing hMSCs with telomerase reverse transcriptase (hMSCs-TERT). The use of these cells is ideal for functional studies of osteoblast and adipocyte differentiation through genetic manipulation, providing a stable and reliable model. Here, we have engineered a stable CAS9 expressing hMSC-TERT cell line (hMSC-TERTCAS9) via lentiviral transduction. The constitutive expression of spCas9 enables efficient and reproducible gene editing. We demonstrate the potential of these hMSC-TERTCAS9 cells for generating gene disruptions using plasmid delivery of guide RNAs as a fast and efficient strategy for targeted genome editing. The edited cells can be sorted and expanded as single cells to obtain homogenous clonal cell lines with mono- as well as bi-allelic gene deletions, a crucial step for producing reliable experimental results. We further validate this cell line as a powerful tool for studying gene function during hMSC proliferation and differentiation, providing 3 distinct examples of its utility. Through the generation of indels, single-cell sorting, and clonal selection, we have efficiently inactivated the vitamin D receptor and created both larger (256 nucleotides) gene disruptions in Forkhead box protein O1 and precise removals of a small genomic sequence (73 nucleotides) coding for microRNA MIR675. This novel hMSC-TERTCAS9 cell line represents a significant advancement, offering a stable, efficient, and versatile platform for advanced genetic studies, high-throughput screening, and the creation of reliable cellular disease models.

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CRISPR-Cas9 differentiation disease modeling gene inactivation hMSC-TERTCAS9 gene editing osteoblasts stem cell research Journal Article

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Ines Foessl, Yuan Guo, Rosinda Mies, Moustapha Kassem, Johannes P T M van Leeuwen, Bram C J van der Eerden, Barbara Obermayer-Pietsch, Jeroen van de Peppel. 2026-07-21. Generation of spCAS9 expressing human mesenchymal stem cell line to study gene function during osteoblast differentiation.. https://doi.org/10.1093/jbmrpl/ziag117

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