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Journal of Translational Medicine
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 ResearchHuman fallopian tube: a new source of multipotent adult mesenchymal stem cells discarded in surgical proceduresTatiana Jazedje1 , Paulo M Perin2 , Carlos E Czeresnia3 , Mariangela Maluf2 , Silvio Halpern2 , Mariane Secco1 , Daniela F Bueno1 , Natassia M Vieira1 , Eder Zucconi1 and Mayana Zatz1  1
Human Genome Research Center, Biosciences Institute, University of São Paulo, Brazil Rua do Matão, n° 106, Cidade Universitária São Paulo SP, CEP: 05508-090, Brazil 2
CEERH Specialized Center for Human Reproduction, São Paulo, Brazil Rua Mato Grosso, n° 306 19° andar, Higienópolis São Paulo SP, CEP: 01239-040, Brazil 3
Celula Mater, São Paulo, Brazil Al. Gabriel Monteiro da Silva, n° 802 São Paulo SP, CEP: 01442-000, Brazil author email corresponding author email
Journal of Translational Medicine 2009,
7:46doi:10.1186/1479-5876-7-46 Abstract
Background
The possibility of using stem cells for regenerative medicine has opened a new field of investigation. The search for sources to obtain multipotent stem cells from discarded tissues or through non-invasive procedures is of great interest. It has been shown that mesenchymal stem cells (MSCs) obtained from umbilical cords, dental pulp and adipose tissue, which are all biological discards, are able to differentiate into muscle, fat, bone and cartilage cell lineages. The aim of this study was to isolate, expand, characterize and assess the differentiation potential of MSCs from human fallopian tubes (hFTs).
Methods
Lineages of hFTs were expanded, had their karyotype analyzed, were characterized by flow cytometry and underwent in vitro adipogenic, chondrogenic, osteogenic, and myogenic differentiation.
Results
Here we show for the first time that hFTs, which are discarded after some gynecological procedures, are a rich additional source of MSCs, which we designated as human tube MSCs (htMSCs).
Conclusion
Human tube MSCs can be easily isolated, expanded in vitro, present a mesenchymal profile and are able to differentiate into muscle, fat, cartilage and bone in vitro. |