解凍後可分離出睪丸幹細胞
再以注射方式注入睪丸組織
獲得精睪丸細胞與精蟲細胞再生
http://humrep.oxfordjournals.org/content/28/4/897.abstract
Spermatogonial stem cell preservation and transplantation: from research to clinic
+Author Affiliations
- ↵*Correspondence address. Tel: +32-2-474-92-13; Fax: +32-2-477-46-32; E-mail: ellen.goossens@uzbrussel.be
- Received December 13, 2012.
- Revision received January 17, 2013.
- Accepted January 28, 2013.
Abstract
STUDY QUESTION What issues remain to be solved before fertility preservation and transplantation can be offered to prepubertal boys?
SUMMARY ANSWER The main issues that need further investigation are malignant cell decontamination, improvement of in vivo fertility restoration and in vitro maturation.
WHAT IS KNOWN ALREADY Prepubertal boys who need gonadotoxic treatment might render sterile for the rest of their life. As these boys do not yet produce sperm cells, they cannot benefit from sperm banking. Spermatogonial stem cell (SSC) banking followed by autologous transplantation has been proposed as a fertility preservation strategy. But before this technique can be applied in the clinic, some important issues have to be resolved.
STUDY DESIGN, SIZE DURATION Original articles as well as review articles published in English were included in a search of the literature.
PARTICIPANTS/MATERIALS, SETTING, METHODS Relevant studies were selected by an extensive Medline search. Search terms were fertility preservation, cryopreservation, prepubertal, SSC, testis tissue, transplantation, grafting and in vitro spermatogenesis. The final number of studies selected for this review was 102.
MAIN RESULTS AND THE ROLE OF CHANCE Cryopreservation protocols for testicular tissue have been developed and are already being used in the clinic. Since the efficiency and safety of SSC transplantation have been reported in mice, transplantation methods are now being adapted to the human testes. Very recently, a few publications reported onin vitro spermatogenesis in mice, but this technique is still far from being applied in a clinical setting.
LIMITATIONS, REASONS FOR CAUTION Using tissue from cancer patients holds a potential risk for contamination of the collected testicular tissue. Therefore, it is of immense importance to separate malignant cells from the cell suspension before transplantation. Because biopsies obtained from young boys are small and contain only few SSCs, propagation of these cells in vitro will be necessary.
WIDER IMPLICATIONS OF THE FINDINGS The ultimate use of the banked tissue will depend on the patient's disease. If the patient was suffering from a non-malignant disease, tissue grafting might be offered. In cancer patients, decontaminated cell suspensions will be injected in the testis. For patients with Klinefelter syndrome, the only option would be in vitro spermatogenesis. However, at present, restoring fertility in cancer and Klinefelter patients is not yet possible.
STUDY FUNDING/COMPETING INTEREST(S) Research Foundation, Flanders (G.0385.08 to H.T.), the Institute for the Agency for Innovation, Belgium (IWT/SB/111245 to E.G.), the Flemish League against Cancer (to E.G.), Kom op tegen kanker (G.0547.11 to H.T.) and the Fund Willy Gepts (to HT). E.G. is a Postdoctoral Fellow of the FWO, Research Foundation, Flanders. There are no conflicts of interest.
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