Anoxia Rapidly Induces Changes in Expression of a Large and Diverse Set of Genes in Endothelial Cells.
Antonella AntonelliEmanuele Salvatore ScarpaSantina BruzzoneCecilia AstigianoFrancesco PiacenteMichela BruschiAlessandra FraternaleChristian Andrea Di BuduoAlessandra BalduiniMauro MagnaniPublished in: International journal of molecular sciences (2023)
Sinusoidal endothelial cells are the predominant vascular surface of the bone marrow and constitute the functional hematopoietic niche where hematopoietic stem and progenitor cells receive cues for self-renewal, survival, and differentiation. In the bone marrow hematopoietic niche, the oxygen tension is usually very low, and this condition affects stem and progenitor cell proliferation and differentiation and other important functions of this region. Here, we have investigated in vitro the response of endothelial cells to a marked decrease in O 2 partial pressure to understand how the basal gene expression of some relevant biological factors (i.e., chemokines and interleukins) that are fundamental for the intercellular communication could change in anoxic conditions. Interestingly, mRNA levels of CXCL3 , CXCL5 , and IL-34 genes are upregulated after anoxia exposure but become downmodulated by sirtuin 6 (SIRT6) overexpression. Indeed, the expression levels of some other genes (such as Leukemia Inhibitory Factor ( LIF )) that were not significantly affected by 8 h anoxia exposure become upregulated in the presence of SIRT6. Therefore, SIRT6 mediates also the endothelial cellular response through the modulation of selected genes in an extreme hypoxic condition.
Keyphrases
- bone marrow
- endothelial cells
- genome wide
- gene expression
- poor prognosis
- mesenchymal stem cells
- bioinformatics analysis
- genome wide identification
- dna methylation
- high glucose
- oxidative stress
- binding protein
- transcription factor
- ischemia reperfusion injury
- acute myeloid leukemia
- vascular endothelial growth factor
- single molecule
- free survival