Long term-cultured and cryopreserved primordial germ cells from various chicken breeds retain high proliferative potential and gonadal colonisation competency

2016 ◽  
Vol 28 (5) ◽  
pp. 628 ◽  
Author(s):  
Céline Tonus ◽  
Karine Cloquette ◽  
Fabien Ectors ◽  
Joëlle Piret ◽  
Laurent Gillet ◽  
...  

When derived from chicken embryos, avian primordial germ cells (PGCs) have been reported to keep their germline-specific properties and proliferative potential even after long-term culture and genetic modifications. Few teams to date have reported such long-term expansion and engineering without differentiation of primary avian PGCs’ cultures. We have developed original and robust methods that allow more than 1 year culture, expansion and cryobanking of primary cultures of PGCs without obvious effects on their biological properties, including their ability to colonise the genital ridges. Overall, 38% of embryonic samples gave rise to PGCs lines derived from three commercial layers and two Belgian endangered breeds. The lines kept their proliferative potential and their characteristic PGCs phenotype after 20 months in culture, whether or not interrupted by a cryopreservation step. All the resulting lines appeared devoid of female cells, although initially pooled from male and female embryos. Labelled PGCs from 12 long-term cultured lines colonised the genital ridges of recipient embryos. Thus, this procedure allows derivation, long-term expansion and cryobanking of primary cultures of PGCs without obvious changes to their original characteristics, providing an alternative access to applications in avian biotechnology and preservation of genetic resources.

Nature ◽  
1992 ◽  
Vol 359 (6395) ◽  
pp. 550-551 ◽  
Author(s):  
James L. Resnick ◽  
Lynn S. Bixler ◽  
Linzhao Cheng ◽  
Peter J. Donovan

Reproduction ◽  
2013 ◽  
Vol 146 (1) ◽  
pp. R37-R48 ◽  
Author(s):  
Jessica M Stringer ◽  
Sanna Barrand ◽  
Patrick Western

In mice, epiblast cells found both the germ-line and somatic lineages in the developing embryo. These epiblast cells carry epigenetic information from both parents that is required for development and cell function in the fetus and during post-natal life. However, germ cells must establish an epigenetic program that supports totipotency and the configuration of parent-specific epigenetic states in the gametes. To achieve this, the epigenetic information inherited by the primordial germ cells at specification is erased and new epigenetic states are established during development of the male and female germ-lines. Errors in this process can lead to transmission of epimutations through the germ-line, which have the potential to affect development and disease in the parent's progeny. This review discusses epigenetic reprogramming in the germ-line and the transmission of epigenetic information to the following generation.


2019 ◽  
Vol 31 (5) ◽  
pp. 847
Author(s):  
Nana Aduma ◽  
Hiroe Izumi ◽  
Shusei Mizushima ◽  
Asato Kuroiwa

DEAD-box helicase 4 (DDX4; also known as vasa) is essential for the proper formation and maintenance of germ cells. Although DDX4 is conserved in a variety of vertebrates and invertebrates, its roles differ between species. This study investigated the function of DDX4 in chicken embryos by knocking down its expression using retroviral vectors that encoded DDX4-targeting microRNAs. DDX4 was effectively depleted invitro and invivo via this approach. Male and female gonads of DDX4-knockdown embryos contained a decreased number of primordial germ cells, indicating that DDX4 is essential to maintain a normal level of these cells in chicken embryos of both sexes. Expression of doublesex and mab-3 related transcription factor 1 (DMRT1) and sex determining region Y-box 9 (SOX9), which are involved in testis determination and differentiation, was normal in male gonads of DDX4-knockdown embryos. In contrast, expression of cytochrome P450 family 19 subfamily A member 1 (CYP19A1), which encodes aromatase and is essential for ovary development, was significantly decreased in female gonads of DDX4-knockdown embryos. Expression of forkhead box L2 (FOXL2), which plays an important role in ovary differentiation, was also slightly reduced in DDX4-knockdown embryos, but not significantly. Based on several pieces of evidence FOXL2 was hypothesised to regulate aromatase expression. The results of this study indicate that aromatase expression is also regulated by several additional pathways.


2014 ◽  
Vol 90 (1) ◽  
Author(s):  
Yonghong Song ◽  
Sivakumar Duraisamy ◽  
Jahabar Ali ◽  
Jaleel Kizhakkayil ◽  
Victor Doss Jacob ◽  
...  

2009 ◽  
Vol 21 (5) ◽  
pp. 696 ◽  
Author(s):  
Sandeep Goel ◽  
Mayako Fujihara ◽  
Kazuo Tsuchiya ◽  
Yuji Takagi ◽  
Naojiro Minami ◽  
...  

Gonocytes are progenitor-type germ cells that arise from primordial germ cells and differentiate further into spermatogonia, thereby initiating spermatogenesis. In the present study, freshly isolated gonocytes were found to have either weak or no expression of pluripotency determining transcription factors, such as POU5F1, SOX2 and C-MYC. Interestingly, the expression of these transcription factors, as well as other vital transcription factors, such as NANOG, KLF4 and DAZL, were markedly upregulated in cultured cells. Cells in primary cultures expressed specific germ cell and pluripotency markers, such as lectin Dolichos biflorus agglutinin (DBA), KIT, ZBTB16, stage-specific embryonic antigen (SSEA-1), NANOG and POU5F1. Using a monoclonal antibody to specifically identify porcine germ cells, the stem cell potential of fresh and cultured cells was determined with a testis xenotransplantation assay. Colonised porcine germ cells were detected only in mouse testes that were either transplanted with fresh testicular cells or with cells from primary cultures. Interestingly, testes transplanted with cells from primary cultures showed colonisation of germ cells in the interstitial space, reflecting their tumourigenic nature. The formation of teratomas with tissues originating from the three germinal layers following the subcutaneous injection of cells into nude mice from primary cultures confirmed their multipotency. The results of the present study may provide useful information for the establishment of multipotent germ stem cell lines from neonatal pig testis.


Author(s):  
Е.П. Федорова ◽  
О.В. Неупокоева ◽  
Л.А. Ставрова ◽  
О.Л. Воронова ◽  
Л.А. Сандрикина ◽  
...  

Выявлено генотоксичное воздействие паклитаксела на хромосомный материал дифференцированных клеток костного мозга самцов и самок мышей в ранние и отдаленные сроки исследования. Установлено, что в эти же сроки наблюдения паклитаксел вызывает гипоплазию костного мозга и снижает в костном мозге экспериментальных животных количество ранних клеток-предшественников эритропоэза, а также способствует уменьшению их пролиферативного потенциала независимо от пола. The genotoxic effect of paclitaxel on the chromosomal material of differentiated bone marrow cells in male and female mice was revealed in the early and long-term periods of the study. It was found that during the same observation period paclitaxel causes bone marrow hypoplasia and reduces the number of early erythropoiesis progenitor cells in the bone marrow of experimental animals, and also contributes to a decrease in their proliferative potential regardless of gender.


2019 ◽  
Vol 242 (1) ◽  
pp. T51-T68 ◽  
Author(s):  
Patrycja A Jazwiec ◽  
Deborah M Sloboda

It is well established that early life environmental signals, including nutrition, set the stage for long-term health and disease risk – effects that span multiple generations. This relationship begins early, in the periconceptional period and extends into embryonic, fetal and early infant phases of life. Now known as the Developmental Origins of Health and Disease (DOHaD), this concept describes the adaptations that a developing organism makes in response to early life cues, resulting in adjustments in homeostatic systems that may prove maladaptive in postnatal life, leading to an increased risk of chronic disease and/or the inheritance of risk factors across generations. Reproductive maturation and function is similarly influenced by early life events. This should not be surprising, since primordial germ cells are established early in life and thus vulnerable to early life adversity. A multitude of ‘modifying’ cues inducing developmental adaptations have been identified that result in changes in reproductive development and impairments in reproductive function. Many types of nutritional challenges including caloric restriction, macronutrient excess and micronutrient insufficiencies have been shown to induce early life adaptations that produce long-term reproductive dysfunction. Many pathways have been suggested to underpin these associations, including epigenetic reprogramming of germ cells. While the mechanisms still remain to be fully investigated, it is clear that a lifecourse approach to understanding lifetime reproductive function is necessary. Furthermore, investigations of the impacts of early life adversity must be extended to include the paternal environment, especially in epidemiological and clinical studies of offspring reproductive function.


Development ◽  
1957 ◽  
Vol 5 (4) ◽  
pp. 396-403
Author(s):  
Beatrice Mintz

The pleiotropic mutant genes W and Wv are alleles of w in the mouse, and produce anaemia, absence of fur pigmentation, and sterility in homozygotes (review by Russell, 1954). Germ-cells of both male and female homozygotes are lacking or drastically reduced in numbers at birth, the genotypes being identifiable through the concurrent anaemia. The developmental basis for this sterility was therefore sought in embryonic life and has been described (Mintz & Russell, 1955, 1957). Recently, a new mutation, Wj, with comparable effects in the homozygote, arose at the same locus. Evidence that it is an allele of the W-series, but different from W or Wv, will be presented elsewhere (Russell, Lawson, & Schabtach, in preparation). In the present report, the early abnormalities characterizing WjWj will be traced and compared with those produced by the other mutant alleles, and will be considered in relation to the problems of germ-cell origin and pleiotropism. A preliminary note (Mintz, 1957) has appeared on the study.


2000 ◽  
Vol 53 (5) ◽  
pp. 1071-1079 ◽  
Author(s):  
B. Kühholzer ◽  
A. Baguisi ◽  
E.W. Overström

Sign in / Sign up

Export Citation Format

Share Document