Use of postmortem human dura mater and scalp for deriving human fibroblast cultures

Fibroblasts can be collected from deceased individuals, grown in culture, reprogrammed into induced pluripotent stem cells (iPSCs), and then differentiated into a multitude of cell types, including neurons. Past studies have generated iPSCs from somatic cell biopsies from either animal or human subj...

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Veröffentlicht in:PloS one 2012-09, Vol.7 (9), p.e45282-e45282
Hauptverfasser: Bliss, Lindsay A, Sams, Malik R, Deep-Soboslay, Amy, Ren-Patterson, Renee, Jaffe, Andrew E, Chenoweth, Josh G, Jaishankar, Amritha, Kleinman, Joel E, Hyde, Thomas M
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Sprache:eng
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Zusammenfassung:Fibroblasts can be collected from deceased individuals, grown in culture, reprogrammed into induced pluripotent stem cells (iPSCs), and then differentiated into a multitude of cell types, including neurons. Past studies have generated iPSCs from somatic cell biopsies from either animal or human subjects. Previously, fibroblasts have only been successfully cultured from postmortem human skin in two studies. Here we present data on fibroblast cell cultures generated from 146 scalp and/or 53 dura mater samples from 146 postmortem human brain donors. In our overall sample, the odds of successful dural culture was almost two-fold compared with scalp (OR = 1.95, 95% CI: [1.01, 3.9], p = 0.047). Using a paired design within subjects for whom both tissues were available for culture (n = 53), the odds of success for culture in dura was 16-fold as compared to scalp (OR = 16.0, 95% CI: [2.1-120.6], p = 0.0007). Unattended death, tissue donation source, longer postmortem interval (PMI), and higher body mass index (BMI) were associated with unsuccessful culture in scalp (all p
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0045282