In Vitro Culture-Induced Pluripotency of Human Spermatogonial Stem Cells

Unipotent spermatogonial stem cells (SSCs) can be transformed into ESC-like cells that exhibit pluripotency in vitro. However, except for mouse models, their characterization and their origins have remained controversies in other models including humans. This controversy has arisen primarily from th...

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Main Authors: Jung Jin Lim, Hyung Joon Kim, Kye-Seong Kim, Jae Yup Hong, Dong Ryul Lee
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2013/143028
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spelling doaj-efafebafce03430b8e1128a761d036742020-11-24T23:08:22ZengHindawi LimitedBioMed Research International2314-61332314-61412013-01-01201310.1155/2013/143028143028In Vitro Culture-Induced Pluripotency of Human Spermatogonial Stem CellsJung Jin Lim0Hyung Joon Kim1Kye-Seong Kim2Jae Yup Hong3Dong Ryul Lee4Fertility Center of CHA Gangnam Medical Center, College of Medicine, CHA University, 606-5 Yeoksam-dong, Gangnam-gu, Seoul 135-081, Republic of KoreaFertility Center of CHA Gangnam Medical Center, College of Medicine, CHA University, 606-5 Yeoksam-dong, Gangnam-gu, Seoul 135-081, Republic of KoreaDepartment of Anatomy and Cell Biology, College of Medicine, Hanyang University, Seoul 133-791, Republic of KoreaDepartment of Urology, CHA Bundang Medical Center, CHA University, Seongnam 463-712, Republic of KoreaFertility Center of CHA Gangnam Medical Center, College of Medicine, CHA University, 606-5 Yeoksam-dong, Gangnam-gu, Seoul 135-081, Republic of KoreaUnipotent spermatogonial stem cells (SSCs) can be transformed into ESC-like cells that exhibit pluripotency in vitro. However, except for mouse models, their characterization and their origins have remained controversies in other models including humans. This controversy has arisen primarily from the lack of the direct induction of ESC-like cells from well-characterized SSCs. Thus, the aim of the present study was to find and characterize pluripotent human SSCs in in vitro cultures of characterized SSCs. Human testicular tissues were dissociated and plated onto gelatin/laminin-coated dishes to isolate SSCs. In the presence of growth factors SSCs formed multicellular clumps after 2–4 weeks of culture. At passages 1 and 5, the clumps were dissociated and were then analyzed using markers of pluripotent cells. The number of SSEA-4-positive cells was extremely low but increased gradually up to ~ 10% in the SSC clumps during culture. Most of the SSEA-4-negative cells expressed markers for SSCs, and some cells coexpressed markers of both pluripotent and germ cells. The pluripotent cells formed embryoid bodies and teratomas that contained derivatives of the three germ layers in SCID mice. These results suggest that the pluripotent cells present within the clumps were derived directly from SSCs during in vitro culture.http://dx.doi.org/10.1155/2013/143028
collection DOAJ
language English
format Article
sources DOAJ
author Jung Jin Lim
Hyung Joon Kim
Kye-Seong Kim
Jae Yup Hong
Dong Ryul Lee
spellingShingle Jung Jin Lim
Hyung Joon Kim
Kye-Seong Kim
Jae Yup Hong
Dong Ryul Lee
In Vitro Culture-Induced Pluripotency of Human Spermatogonial Stem Cells
BioMed Research International
author_facet Jung Jin Lim
Hyung Joon Kim
Kye-Seong Kim
Jae Yup Hong
Dong Ryul Lee
author_sort Jung Jin Lim
title In Vitro Culture-Induced Pluripotency of Human Spermatogonial Stem Cells
title_short In Vitro Culture-Induced Pluripotency of Human Spermatogonial Stem Cells
title_full In Vitro Culture-Induced Pluripotency of Human Spermatogonial Stem Cells
title_fullStr In Vitro Culture-Induced Pluripotency of Human Spermatogonial Stem Cells
title_full_unstemmed In Vitro Culture-Induced Pluripotency of Human Spermatogonial Stem Cells
title_sort in vitro culture-induced pluripotency of human spermatogonial stem cells
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2013-01-01
description Unipotent spermatogonial stem cells (SSCs) can be transformed into ESC-like cells that exhibit pluripotency in vitro. However, except for mouse models, their characterization and their origins have remained controversies in other models including humans. This controversy has arisen primarily from the lack of the direct induction of ESC-like cells from well-characterized SSCs. Thus, the aim of the present study was to find and characterize pluripotent human SSCs in in vitro cultures of characterized SSCs. Human testicular tissues were dissociated and plated onto gelatin/laminin-coated dishes to isolate SSCs. In the presence of growth factors SSCs formed multicellular clumps after 2–4 weeks of culture. At passages 1 and 5, the clumps were dissociated and were then analyzed using markers of pluripotent cells. The number of SSEA-4-positive cells was extremely low but increased gradually up to ~ 10% in the SSC clumps during culture. Most of the SSEA-4-negative cells expressed markers for SSCs, and some cells coexpressed markers of both pluripotent and germ cells. The pluripotent cells formed embryoid bodies and teratomas that contained derivatives of the three germ layers in SCID mice. These results suggest that the pluripotent cells present within the clumps were derived directly from SSCs during in vitro culture.
url http://dx.doi.org/10.1155/2013/143028
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