Xeno-free propagation of spermatogonial stem cells from infant boys

dc.authorid0000-0002-6605-9641
dc.authorid0000-0002-6657-6227
dc.authorid0000-0002-6639-0625
dc.authorid0000-0003-1546-1945
dc.authorid0000-0003-1194-8393
dc.contributor.authorDong, Lihua
dc.contributor.authorGül, Murat
dc.contributor.authorHildorf, Simone
dc.contributor.authorSusanne Elisabeth
dc.contributor.authorKristensen, Stine Gry
dc.contributor.authorHoffmann, Eva R.
dc.contributor.authorCortes, Dina
dc.contributor.authorThorup, Jorgen Mogens
dc.contributor.authorAndersen, Claus Yding
dc.date.accessioned2019-11-26T13:45:03Z
dc.date.available2019-11-26T13:45:03Z
dc.date.issued2019
dc.departmentTıp Fakültesi
dc.descriptionGül, Murat ( Aksaray, Yazar )
dc.description.abstractSpermatogonial stem cell (SSC) transplantation therapy is a promising strategy to renew spermatogenesis for prepubertal boys whose fertility is compromised. However, propagation of SSCs is required due to a limited number of SSCs in cryopreserved testicular tissue. This propagation must be done under xeno-free conditions for clinical application. SSCs were propagated from infant testicular tissue (7 mg and 10 mg) from two boys under xeno-free conditions using human platelet lysate and nutrient source. We verified SSC-like cell clusters (SSCLCs) by quantitative real-time polymerase chain reaction (PCR) and immune-reaction assay using the SSC markers undifferentiated embryonic cell transcription factor 1 (UTF1), ubiquitin carboxyl-terminal hydrolase isozyme L1 (UCHL1), GDNF receptor alpha-1 (GFR?-1) F? and promyelocytic leukaemia zinc finger protein (PLZF). The functionality of the propagated SSCs was investigated by pre-labelling using green fluorescent Cell Linker PKH67 and xeno-transplantation of the SSCLCs into busulfan-treated, therefore sterile, immunodeficient mice. SSC-like cell clusters (SSCLCs) appeared after 2 weeks in primary passage. The SSCLCs were SSC-like as the UTF1, UCHL1, GFR?1 and PLZF were all positive. After 2.5 months’ culture period, a total of 13 million cells from one sample were harvested for xenotransplantation. Labelled human propagated SSCs were identified and verified in mouse seminiferous tubules at 3–6 weeks, confirming that the transplanted cells contain SSCLCs. The present xeno-free clinical culture protocol allows propagation of SSCs from infant boys.
dc.description.abstract...
dc.identifier.doi10.3390/ijms20215390
dc.identifier.endpage-en_US
dc.identifier.issn1661-6596
dc.identifier.issue21en_US
dc.identifier.scopusqualityQ1
dc.identifier.startpage-en_US
dc.identifier.urihttps://dx.doi.org.10.3390/ijms20215390
dc.identifier.urihttps://hdl.handle.net/20.500.12451/6990
dc.identifier.volume20en_US
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMDPI AG
dc.relation.ispartofInternational Journal of Molecular Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectSpermatogonial Stem Cells
dc.subjectMale Fertility Cryopreservation
dc.subjectXeno-transplantation
dc.subjectIn vitro propagation
dc.subjectXeno-free Culture
dc.titleXeno-free propagation of spermatogonial stem cells from infant boys
dc.typeArticle

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