Effect of 3D Spheroid Culturing on NF-κB Signaling Pathway and Neurogenic Potential in Human Amniotic Fluid Stem Cells

• Published in: International journal of molecular sciences 2023-02, Vol.24 (4), p.3584
• Main Authors: Valiulienė, Giedrė, Zentelytė, Aistė, Beržanskytė, Elizabet, Navakauskienė, Rūta
• Format: Article
• Language: English
• Subjects: Amniotic fluid; Amniotic Fluid - metabolism; Antigens; Bone marrow; Cell adhesion & migration; Cell culture; Cell Culture Techniques, Three Dimensional - methods; Cell Differentiation; Comparative analysis; Differentiation; Extracellular matrix; Female; Flow cytometry; Gene expression; Genes; human amniotic fluid stem cells (hAFSCs); Humans; Instrument industry; Kinases; MicroRNAs; Morphology; Msi1 protein; Nerve Tissue Proteins - metabolism; neural differentiation; NF-kappa B - metabolism; NF-κB; NF-κB protein; Oct-4 protein; Pluripotency; Pregnancy; Protein expression; Proteins; RNA-Binding Proteins - metabolism; Scientific equipment and supplies industry; Secretome; Signal Transduction; Spheroids; Spheroids, Cellular; Stem cells; Stem Cells - metabolism; Synaptotagmin; three-dimensional (3D) spheroid cultures; Transcription factors
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms24043584

Human amniotic fluid stem cells (hAFSCs) are known for their advantageous properties when compared to somatic stem cells from other sources. Recently hAFSCs have gained attention for their neurogenic potential and secretory profile. However, hAFSCs in three-dimensional (3D) cultures remain poorly investigated. Therefore, we aimed to evaluate cellular properties, neural differentiation, and gene and protein expression in 3D spheroid cultures of hAFSCs in comparison to traditional two-dimensional (2D) monolayer cultures. For this purpose, hAFSCs were obtained from amniotic fluid of healthy pregnancies and cultivated in vitro, either in 2D, or 3D under untreated or neuro-differentiated conditions. We observed upregulated expression of pluripotency genes , , and as well as augmentation in gene expression of NF-κB-TNFα pathway genes ( , and ), associated miRNAs (miR103a-5p, miR199a-3p and miR223-3p), and NF-κB p65 protein levels in untreated hAFSC 3D cultures. Additionally, MS analysis of the 3D hAFSCs secretome revealed protein upregulation of IGFs signaling the cascade and downregulation of extracellular matrix proteins, whereas neural differentiation of hAFSC spheroids increased the expression of miR223-3p, and MSI1. Summarizing, our study provides novel insights into how 3D culture affects neurogenic potential and signaling pathways of hAFSCs, especially NF-κB, although further studies are needed to elucidate the benefits of 3D cultures more thoroughly.