AI Article Synopsis

  • The dataset outlines a method to isolate mesenchymal cells from human fat without using collagenase.
  • Fat specimens are cleaned of non-fat tissues and incubated in culture media, allowing cells to grow and spread over five to seven days.
  • Results show that primary cells initially display varied shapes but become more uniform over time, with efficiency and doubling time metrics provided in additional figures.

Article Abstract

The present dataset describes a detailed protocol to isolate mesenchymal cells from human fat without the use of collagenase. Human fat specimen, surgically cleaned from non-fat tissues (e.g., blood vessels) and reduced into smaller fat pieces of around 1-3 mm size, is incubated in complete culture media for five to seven days. Then, cells started to spread out from the fat explants and to grow in cultures according to an exponential pattern. Our data showed that primary mesenchymal cells presenting heterogeneous morphology start to acquire more homogenous fibroblastic-like shape when cultured for longer duration or when subcultured into new flasks. Cell isolation efficiency as well as cell doubling time were also calculated throughout the culturing experimentations and illustrated in a separate figure thereafter. This paper contains data previously considered as an alternative protocol to isolate adipose-derived mesenchymal stem cell published in "Proliferation and differentiation of human adipose-derived mesenchymal stem cells (ASCs) into osteoblastic lineage are passage dependent" [1].

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760183PMC
http://dx.doi.org/10.1016/j.dib.2016.02.002DOI Listing

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