Generation and characterization of transgenic mouse mesenchymal stem cell lines expressing hIGF-1 or hG-CSF.
Gabrielle V M GonçalvesDaniela N SilvaRejane H CarvalhoBruno S F SouzaKátia Nunes da SilvaJuliana F VasconcelosBruno D ParedesCarolina K V NonakaRicardo Ribeiro-Dos-SantosMilena Botelho Pereira SoaresPublished in: Cytotechnology (2017)
Mesenchymal stem cells (MSC) are promising tools in the fields of cell therapy and regenerative medicine. In addition to their differentiation potential, MSC have the ability to secrete bioactive molecules that stimulate tissue regeneration. Thus, the overexpression of cytokines and growth factors may enhance the therapeutic effects of MSC. Here we generated and characterized mouse bone marrow MSC lines overexpressing hG-CSF or hIGF-1. MSC lines overexpressing hG-CSF or hIGF-1 were generated through lentiviral vector mediated gene transfer. The expression of hG-CSF or hIGF-1 genes in the clones produced was quantified by qRT-PCR, and the proteins were detected in the cell supernatants by ELISA. The cell lines displayed cell surface markers and differentiation potential into adipocytes, osteocytes and chondrocytes similar to the control MSC cell lines, indicating the conservation of their phenotype even after genetic modification. IGF-1 and G-CSF transgenic cells maintained immunosuppressive activity. Finally, we performed a comparative gene expression analysis by qRT-PCR array in the cell lines expressing hIGF-1 and hG-CSF when compared to the control cells. Our results demonstrate that the cell lines generated may be useful tools for cell therapy and are suitable for testing in disease models.
Keyphrases
- cell therapy
- mesenchymal stem cells
- bone marrow
- stem cells
- umbilical cord
- fluorescent probe
- induced apoptosis
- genome wide
- genome wide identification
- cell cycle arrest
- living cells
- copy number
- cerebrospinal fluid
- aqueous solution
- cell surface
- adipose tissue
- cell proliferation
- poor prognosis
- type diabetes
- skeletal muscle
- pi k akt
- high throughput
- endoplasmic reticulum stress
- signaling pathway
- high resolution
- oxidative stress
- climate change
- insulin resistance
- gene expression