Scholarlink

Background <p>Mesenchymal stromal cells (MSCs) exert therapeutic effects primarily through their secretome, rich in bioactive factors with immunomodulatory and regenerative properties. However, clinical application of MSC-derived secretome is hindered by donor variability, limited expansion, and replicative senescence. To address these issues, we developed immortalized human hair follicle-derived mesenchymal-like stromal cells (iHF-MSCs) as a consistent and scalable source of therapeutic secretome.</p> Methods <p>HF-MSCs were isolated using a minimally invasive procedure and immortalized with lentiviral SV40 large T antigen. From 576 single-cell clones, C18 and C26 were selected based on proliferation capacity, absence of senescence, and retention of a mesenchymal-like phenotype. Characterization included RT-PCR, flow cytometry for surface markers, trilineage differentiation, and CD56 expression analysis. For immunomodulatory evaluation, cells were licensed with IFN-γ and TNF-α, and the resulting conditioned media (licensed CM) were analyzed by ELISA and cytokine arrays. PBMC proliferation and Treg induction were assessed using licensed CM, while unlicensed CM was tested for its regenerative effects on dermal and epidermal cell functions, including wound repair, tube formation assay as an indicator of angiogenic potential, and oxidative stress response.</p> Results <p>The selected clones (C18 and C26) exhibited long-term stability, rapid expansion, and preserved mesenchymal-like phenotype and multipotency. Secretome profiling revealed an enriched composition of immunoregulatory (e.g., Gal-9, IL-1Ra, TSG-6) and pro-regenerative (e.g., VEGF, PDGF-AA, EGF) factors, with enhanced responsiveness to inflammatory licensing. Notably, iHF-MSCs maintained low immunogenicity and demonstrated superior functional performance: inhibition of PBMC proliferation, Treg induction, and promotion of skin cell proliferation, migration, tube formation, and oxidative stress protection.</p> Conclusion <p>These results position iHF-MSCs as a robust and scalable platform for consistent production of therapeutic secretome, paving the way for innovative, cell-free immunomodulatory and regenerative therapies.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Immortalized human hair follicle-derived mesenchymal-like stromal cells for the long-term production of scalable Immunomodulatory and regenerative secretome

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年11月17日

查看全文
  • Maria Rossello-Gelabert,
  • Kevin Las Heras,
  • Ainhoa Gonzalez-Pujana,
  • Manoli Igartua,
  • Edorta Santos-Vizcaino,
  • Rosa Maria Hernandez

摘要

Background

Mesenchymal stromal cells (MSCs) exert therapeutic effects primarily through their secretome, rich in bioactive factors with immunomodulatory and regenerative properties. However, clinical application of MSC-derived secretome is hindered by donor variability, limited expansion, and replicative senescence. To address these issues, we developed immortalized human hair follicle-derived mesenchymal-like stromal cells (iHF-MSCs) as a consistent and scalable source of therapeutic secretome.

Methods

HF-MSCs were isolated using a minimally invasive procedure and immortalized with lentiviral SV40 large T antigen. From 576 single-cell clones, C18 and C26 were selected based on proliferation capacity, absence of senescence, and retention of a mesenchymal-like phenotype. Characterization included RT-PCR, flow cytometry for surface markers, trilineage differentiation, and CD56 expression analysis. For immunomodulatory evaluation, cells were licensed with IFN-γ and TNF-α, and the resulting conditioned media (licensed CM) were analyzed by ELISA and cytokine arrays. PBMC proliferation and Treg induction were assessed using licensed CM, while unlicensed CM was tested for its regenerative effects on dermal and epidermal cell functions, including wound repair, tube formation assay as an indicator of angiogenic potential, and oxidative stress response.

Results

The selected clones (C18 and C26) exhibited long-term stability, rapid expansion, and preserved mesenchymal-like phenotype and multipotency. Secretome profiling revealed an enriched composition of immunoregulatory (e.g., Gal-9, IL-1Ra, TSG-6) and pro-regenerative (e.g., VEGF, PDGF-AA, EGF) factors, with enhanced responsiveness to inflammatory licensing. Notably, iHF-MSCs maintained low immunogenicity and demonstrated superior functional performance: inhibition of PBMC proliferation, Treg induction, and promotion of skin cell proliferation, migration, tube formation, and oxidative stress protection.

Conclusion

These results position iHF-MSCs as a robust and scalable platform for consistent production of therapeutic secretome, paving the way for innovative, cell-free immunomodulatory and regenerative therapies.