Abstract

There is clinical interest in using human adipose tissue-derived mesenchymal stromal cells (ASC) to treat a range of inflammatory and regenerative conditions. Aspects of ASC biology, including their regenerative potential and paracrine effect, are likely to be modulated, in part, by microRNAs, small RNA molecules that are embedded as regulators of gene-expression in most biological pathways. However, the effect of standard isolation and expansion protocols on microRNA expression in ASC is not well explored. Here, by using an untouched and enriched population of primary human ASC, we demonstrate that there are rapid and significant changes in microRNA expression when ASC are subjected to standard isolation and expansion methods. Functional studies focusing on miR-378 indicate that these changes in expression may have an impact on phenotype and function. Specifically, we found that increased levels of miR-378 significantly promoted adipogenesis in late passage ASC. These results are informative to maximizing the potential of ASC for use in various clinical applications, and they have implications for targeting microRNAs as a therapeutic strategy for obesity or metabolic disease.

Highlights

  • Human adipose tissue derived mesenchymal stromal cells (ASC) are showing promise in the clinic for a range of inflammatory and degenerative conditions [1]. These cells are derived from the heterogeneous stromal vascular fraction (SVF), which is isolated from the lipoaspirate of patients

  • The ex vivo ASC cell surface phenotype was defined as CD45-CD235a-CD31-CD34+ CD13+CD73+CD90+CD105+ by the International Society for Cell and Gene Therapy (ISCT) and International Federation for Adipose Therapeutics and Science (IFATS) in 2013 [2]

  • We previously reported on culture-induced mRNA changes in ex vivo ASC [3]

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Summary

Introduction

Human adipose tissue derived mesenchymal stromal cells (ASC) are showing promise in the clinic for a range of inflammatory and degenerative conditions [1]. We previously reported a method that allowed for the rapid enrichment of a defined and untouched ex vivo ASC population that were compared to culture-derived ASC [3] This comparison found that ex vivo ASC demonstrate rapid changes in mRNA expression when exposed to adherent-tissue culture that are likely to effect the function and potency of these cells. Here we report that global microRNA expression patterns change rapidly and significantly within days of exposure to adherent tissue culture. This modulation might affect their paracrine effect and clinical utility. Our findings are informative to ASC research, which demonstrates variability in cell isolation and expansion protocols

Results
Processing Lipoaspirate
Culturing SVF to Isolate Culture-Derived ASC
MACS Sorting Cells to Isolate MACS-Derived ASC
Adipogenic Differentiation Assays
Microarrays
RT-PCR
Transfection of Late Passage ASC
Statistical Analysis
Full Text
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