Propagation of spermatogonial stem cell-like cells from infant boys

dc.authorid0000-0001-6841-1998
dc.contributor.authorDong, Lihua
dc.contributor.authorKristensen, Stine Gry
dc.contributor.authorHildorf, Simone
dc.contributor.authorGül, Murat
dc.contributor.authorClasen-Linde, Erik
dc.contributor.authorFedder, Jens
dc.contributor.authorHoffmann, Eva R.
dc.contributor.authorCortes, Dina
dc.contributor.authorThorup, Jorgen
dc.contributor.authorAndersen, Claus Yding
dc.date.accessioned2019-10-17T06:22:46Z
dc.date.available2019-10-17T06:22:46Z
dc.date.issued2019
dc.departmentTıp Fakültesi
dc.description*Gül, Murat ( Aksaray, Yazar )
dc.description.abstractBackground: Gonadotoxic treatment of malignant diseases as well as some nonmalignant conditions such as cryptorchidism in young boys may result in infertility and failure to father children later in life. As a fertility preserving strategy, several centers collect testicular biopsies to cryopreserve spermatogonial stem cells (SSCs) worldwide. One of the most promising therapeutic strategies is to transplant SSCs back into the seminiferous tubules to initiate endogenous spermatogenesis. However, to obtain sufficient numbers of SSC to warrant transplantation, in vitro propagation of cells is needed together with proper validation of their stem cell identity. Materials and Methods: A minute amount of testicular biopsies (between 5 mg and 10 mg) were processed by mechanical and enzymatic digestion. SSCs were enriched by differential plating method in StemPro-34 medium supplemented with several growth factors. SSC-like cell clusters (SSCLCs) were passaged five times. SSCLCs were identified by immunohistochemical and immunofluorescence staining, using protein expression patterns in testis biopsies as reference. Quantitative polymerase chain reaction analysis of SSC markers LIN-28 homolog A (LIN28A), G antigen 1 (GAGE1), promyelocytic leukemia zinc finger protein (PLZF), integrin alpha 6 (ITGA6), ubiquitin carboxy-terminal hydrolase L1 (UCHL1) and integrin beta 1 (ITGB1) were also used to validate the SSC-like cell identity. Results: Proliferation of SSCLCs was achieved. The presence of SSCs in SSCLCs was confirmed by positive immunostaining of LIN28, UCHL1 and quantitative polymerase chain reaction for LIN28A, UCHL1, PLZF, ITGA6, and ITGB1, respectively. Conclusion: This study has demonstrated that SSCs from infant boys possess the capacity for in vitro proliferation and advance a fertility preservation strategy for prepubertal boys who may otherwise lose their fertility.
dc.description.abstract...
dc.identifier.doi10.3389/fphys.2019.01155
dc.identifier.endpage-en_US
dc.identifier.issn0000-1155
dc.identifier.issue-en_US
dc.identifier.scopusqualityQ2
dc.identifier.startpage-en_US
dc.identifier.urihttps://dx.doi.org/10.3389/fphys.2019.01155
dc.identifier.urihttps://hdl.handle.net/20.500.12451/6859
dc.identifier.volume10en_US
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherFrontiers Media
dc.relation.ispartofFrontiers in Physiology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectCryptorchidism
dc.subjectFertility Cryopreservation
dc.subjectIn Vitro Expansion
dc.subjectMale Infertility
dc.subjectSpermatogonial Stem Cell
dc.titlePropagation of spermatogonial stem cell-like cells from infant boys
dc.typeArticle

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