AI Article Synopsis

  • Researchers discovered that Wnt7a increases after muscle injury and is released from regenerating myofibers through exosomes to promote muscle growth.
  • They identified a new methodology combining Tangential Flow Filtration (TFF) and Size Exclusion Chromatography (SEC) to efficiently purify extracellular vesicles (EVs) from muscle tissue, addressing contamination issues seen with traditional methods.
  • This optimized protocol enhances the purity and structural integrity of EVs, making them suitable for various biological assays and applications.

Article Abstract

We have recently made the strikingly discovery that upon a muscle injury, Wnt7a is upregulated and secreted from new regenerating myofibers on the surface of exosomes to elicit its myogenerative response distally. Despite recent advances in extracellular vesicle (EVs) isolation from diverse tissues, there is still a lack of specific methodology to purify EVs from muscle tissue. To eliminate contamination with non-EV secreted proteins and cytoplasmic fragments, which are typically found when using classical methodology, such as ultracentrifugation, we adapted a protocol combining Tangential Flow Filtration (TFF) and Size Exclusion Chromatography (SEC). We found that this approach allows simultaneous purification of Wnt7a, bound to EVs (retentate fraction) and free non-EV Wnt7a (permeate fraction). Here we described this optimized protocol designed to specifically isolate EVs from hind limb muscle explants, without cross-contamination with other sources of non-EV bounded proteins. The first step of the protocol is to remove large EVs with sequential centrifugation. Extracellular vesicles are then concentrated and washed in exchange buffer by TFF. Lastly, SEC is performed to remove any soluble protein traces remaining after TFF. Overall, this procedure can be used to isolate EVs from conditioned media or biofluid that contains EVs derived from any cell type or tissue, improving reproducibility, efficiency, and purity of EVs preparations. Our purification protocol results in high purity EVs that maintain structural integrity and thus fully compatible with in vitro and in vivo bioactivity and analytic assays.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11468478PMC
http://dx.doi.org/10.1186/s13395-024-00355-1DOI Listing

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