Literature DB >> 9364445

The developmental origin of primordial germ cells and the transmission of the donor-derived gametes in mixed-sex germline chimeras to the offspring in the chicken.

H Kagami1, T Tagami, Y Matsubara, T Harumi, H Hanada, K Maruyama, M Sakurai, T Kuwana, M Naito.   

Abstract

A novel system has been developed to determine the origin and development of primordial germ cells (PGCs) in avian embryos directly. Approximately 700 cells were removed from the center of the area pellucida, the outer of the area pellucida, and the area opaca of the stage X blastoderm (Eyal-Giladi and Kochav, 1976; Dev Biol 49:321-337). When the cells were removed from the center of the area pellucida, the mean number of circulating PGCs per 1 microliter of blood was significantly decreased to 13 (P < 0.05) in the embryo at stage 15 (Hamburger and Hamilton, 1951: J Morphol 88:49-92) as compared to intact embryos of 51. When the removed recipient cells from the center of the area pellucida were replenished with 500 donor cells, no reduction in the PGC number was observed. The removal of cells from the outer of area pellucida or from the area opaca had no effect on the number of PGCs. When another set of the manipulated embryos were cultured ex vivo to hatching and reared to sexual maturity, the absence of germ cells and the degeneration of seminiferous tubules were observed in resulting chickens derived from the blastoderm from which the cells were removed from the center of the area pellucida. Chimeric embryos produced by the male donor cells and the female recipient contained the female-derived cells at 97.2% in the whole embryo and 94.3% in the erythrocytes at 5 days of incubation. At 5-7 days of incubation, masculinization was observed in about one half of the mixed-sex embryos. The proportions of the female-derived cells in the whole embryo and in the erythrocytes were 76.5% and 80.2% at 7 days to 55.7% and 62.5% at 10 days of incubation, respectively. When the chimeras reached their sexual maturity, they were test mated to assess donor contribution to their germline. Five of six male chimeras (83%) and three of five female chimeras (60%) from male donor cells and a female recipient embryo from which 700 cells at the center of area pellucida were removed were germline chimeras. Three of the five male germline chimeras (60%) and one of the three female germline chimeras (33%) transmitted exclusively (100%) donor-derived gametes into the offspring. When embryonic cells were removed from the outer of area pellucida or area opaca, regardless of the sex combination of the donor and the recipient, the transmission of the donor-derived gametes was essentially null. The findings in the present studies demonstrated, both in vivo and in vitro, that the PGCs originate in the central part of the area pellucida and that the developmental fate to germ cell (PGCs) had been destined at stage X blastoderm in chickens.

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Year:  1997        PMID: 9364445     DOI: 10.1002/(SICI)1098-2795(199712)48:4<501::AID-MRD11>3.0.CO;2-W

Source DB:  PubMed          Journal:  Mol Reprod Dev        ISSN: 1040-452X            Impact factor:   2.609


  11 in total

1.  Analysis of chicken primordial germ cells.

Authors:  Makoto Motono; Takuya Ohashi; Ken-Ichi Nishijima; Shinji Iijima
Journal:  Cytotechnology       Date:  2008-07-23       Impact factor: 2.058

2.  Gamma-irradiation depletes endogenous germ cells and increases donor cell distribution in chimeric chickens.

Authors:  Kyung Je Park; Seok Jin Kang; Tae Min Kim; Young Mok Lee; Hyung Chul Lee; Gwonhwa Song; Jae Yong Han
Journal:  In Vitro Cell Dev Biol Anim       Date:  2010-11-06       Impact factor: 2.416

3.  Reviving rare chicken breeds using genetically engineered sterility in surrogate host birds.

Authors:  Mark E Woodcock; Almas A Gheyas; Andrew S Mason; Sunil Nandi; Lorna Taylor; Adrian Sherman; Jacqueline Smith; Dave W Burt; Rachel Hawken; Michael J McGrew
Journal:  Proc Natl Acad Sci U S A       Date:  2019-10-01       Impact factor: 11.205

4.  Viable pluripotent chick blastodermal cells can be maintained long term in an alkaline defined medium.

Authors:  María Cruz López-Díaz; Julia Buján-Varela; Carlos Cadórniga-Valiño
Journal:  In Vitro Cell Dev Biol Anim       Date:  2015-12-31       Impact factor: 2.416

5.  Inter embryonic (homo- or hetero-sexual) transfer of primordial germ cells between chicken embryos.

Authors:  H Yamaguchi; Y Xi; N Fujihara
Journal:  Cytotechnology       Date:  2000-07       Impact factor: 2.058

6.  Efficient genetic modification and germ-line transmission of primordial germ cells using piggyBac and Tol2 transposons.

Authors:  Joni Macdonald; Lorna Taylor; Adrian Sherman; Koichi Kawakami; Yoshiko Takahashi; Helen M Sang; Michael J McGrew
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-14       Impact factor: 11.205

7.  Migration and differentiation of gonadal germ cells under cross-sex germline chimeras condition in domestic chickens.

Authors:  Yuki Nakajima; Tetsuya Hattori; Atsushi Asano; Naoto Ishikawa; Atsushi Tajima
Journal:  J Reprod Dev       Date:  2014-08-16       Impact factor: 2.214

Review 8.  Perspectives on avian stem cells for poultry breeding.

Authors:  Hiroshi Kagami
Journal:  Anim Sci J       Date:  2016-05-12       Impact factor: 1.749

Review 9.  Poultry genetic resource conservation using primordial germ cells.

Authors:  Yoshiaki Nakamura
Journal:  J Reprod Dev       Date:  2016-05-21       Impact factor: 2.214

10.  Developmental stages of the blue-breasted quail (Coturnix chinensis).

Authors:  Yoshiaki Nakamura; Yoshifumi Nakane; Masaoki Tsudzuki
Journal:  Anim Sci J       Date:  2018-10-28       Impact factor: 1.749

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