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Hypoxia-Induced Let-7d Has a Role in Pericyte Differentiation
Nilufer Esen1, Anuush Vejalla2, Rakhi Sharma2
1Department of Neurology, Medical School, Wayne State University, Elliman Building, Rm 3125, 421 E. Canfield Str., Detroit, MI, 48201, USA. nesenbil@med.wayne.edu.
Advances in Experimental Medicine and Biology
|August 16, 2016
Summary
Microvascular pericytes adapt to hypoxic stress via microRNAs (miRNAs), particularly Let-7d. This process, involving basic fibroblast growth factor (bFGF), promotes pericyte differentiation and may aid tissue repair.
Area of Science:
- Cell Biology
- Stem Cell Research
- Tissue Engineering
Background:
- Microvascular pericytes are crucial for maintaining tissue homeostasis.
- Pericytes adapt to stress signals through mechanisms like migration, differentiation, and angiogenesis.
- Hypoxic stress (1% O2) induces adaptive changes in pericytes, partly via microRNAs (miRNAs).
Purpose of the Study:
- To investigate pericyte responses to hypoxic stress.
- To determine the role of specific miRNAs, such as Let-7d, in pericyte adaptation.
- To elucidate the pathway involved in hypoxia-induced pericyte differentiation.
Main Methods:
- Pericytes were exposed to hypoxia (1% O2) with and without basic fibroblast growth factor (bFGF) in stem cell medium.
- Let-7d expression in pericyte-derived neurospheres was quantified.
- Immunocytochemistry was used to assess evidence of cell differentiation, including Sox2 expression.
Main Results:
- Hypoxia enhanced pericyte spheres showed increased expression of Let-7d.
- The transcription factor Sox2, a marker of differentiation, was induced in pericytic spheres.
- Basic fibroblast growth factor (bFGF) influenced these hypoxia-induced changes.
Conclusions:
- Pericyte expression of Let-7d in response to hypoxia and bFGF is involved in pericyte differentiation.
- A novel pathway for the induction of pericyte differentiation is proposed.
- Modulating this pathway could be a therapeutic target for tissue repair.

