Mouse differentiating spermatogonia can generate germinal stem cells in vivo

被引:134
作者
Barroca, Vilma [1 ]
Lassalle, Bruno [1 ]
Coureuil, Mathieu [1 ]
Louis, Jean Paul [2 ]
Le Page, Florence [1 ]
Testart, Jacques [1 ]
Allemand, Isabelle [1 ]
Riou, Lydia [1 ]
Fouchet, Pierre [1 ]
机构
[1] CEA, Direct Sci Vivant, Inst Radiobiol Cellulaire & Mol,U566, Lab Gametogenese Apoptose & Genotoxicite,INSERM, F-92265 Fontenay Aux Roses, France
[2] CNRS, UMR 6218, F-45071 Orleans, France
关键词
UNDIFFERENTIATED SPERMATOGONIA; GENETIC-ANALYSIS; SELF-RENEWAL; KIT-LIGAND; C-KIT; SPERMATOGENESIS; TESTIS; NICHE; PROLIFERATION; PLURIPOTENCY;
D O I
10.1038/ncb1826
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In adults, stem cells are responsible for the maintenance of many actively renewing tissues, such as haematopoietic, skin, gut and germinal tissues. These stem cells can self-renew or be committed to becoming progenitors. Stem-cell commitment is thought to be irreversible but in male and female Drosophila melanogaster, it was shown recently that differentiating germ cells can revert to functional stem cells that can restore germinal lineage(1,2). Whether progenitors are also able to generate stem cells in mammals remains unknown. Here we show that purified mouse spermatogonial progenitors committed to differentiation can generate functional germinal stem cells that can repopulate germ-cell-depleted testes when transplanted into adult mice. We found that GDNF, a key regulator of the stem-cell niche, and FGF2 are able to reprogram in vitro spermatogonial progenitors for reverse differentiation. This study supports the emerging concept that the stem-cell identity is not restricted in adults to a definite pool of cells that self-renew, but that stemness could be acquired by differentiating progenitors after tissue injury and throughout life.
引用
收藏
页码:190 / U173
页数:12
相关论文
共 33 条
  • [1] Long-term haematopoietic reconstitution by Trp53-/-p16Ink4a-/-p19Arf-/- multipotent progenitors
    Akala, Omobolaji O.
    Park, In-Kyung
    Qian, Dalong
    Pihalja, Michael
    Becker, Michael W.
    Clarke, Michael F.
    [J]. NATURE, 2008, 453 (7192) : 228 - U12
  • [2] AOI T, 2008, SCIENCE, V26, P101
  • [3] Flow cytometric characterization of viable meiotic and postmeiotic cells by Hoechst 33342 in mouse spermatogenesis
    Bastos, H
    Lassalle, B
    Chicheportiche, A
    Riou, L
    Testart, J
    Allemand, I
    Fouchet, P
    [J]. CYTOMETRY PART A, 2005, 65A (01) : 40 - 49
  • [4] Bedell MA, 2004, J ANDROL, V25, P188
  • [5] Interaction with the mammary microenvironment redirects spermatogenic cell fate in vivo
    Boulanger, Corinne A.
    Mack, David L.
    Booth, Brian W.
    Smith, Gilbert H.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (10) : 3871 - 3876
  • [6] Regeneration of male germline stem cells by spermatogonial dedifferentiation in vivo
    Brawley, C
    Matunis, E
    [J]. SCIENCE, 2004, 304 (5675) : 1331 - 1334
  • [7] ERM is required for transcriptional control of the spermatogonial stem cell niche
    Chen, C
    Ouyang, W
    Grigura, V
    Zhou, Q
    Carnes, K
    Lim, H
    Zhao, GQ
    Arber, S
    Kurpios, N
    Murphy, TL
    Cheng, AM
    Hassell, JA
    Chandrashekar, V
    Hofmann, MC
    Hess, RA
    Murphy, KM
    [J]. NATURE, 2005, 436 (7053) : 1030 - 1034
  • [8] Proliferation and differentiation of spermatogonial stem cells
    de Rooij, DG
    [J]. REPRODUCTION, 2001, 121 (03) : 347 - 354
  • [9] Spermatogonial stem cells
    de Rooij, DG
    Grootegoed, JA
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (06) : 694 - 701
  • [10] Identification and enrichment of spermatogonial stem cells displaying side-population phenotype in immature mouse testis
    Falciatori, I
    Borsellino, G
    Haliassos, N
    Boitani, C
    Corallini, S
    Battistini, L
    Bernardi, G
    Stefanini, M
    Vicini, E
    [J]. FASEB JOURNAL, 2003, 17 (15) : 376 - +