TGF beta 1 inhibits proliferation and has a chemotropic effect on mouse primordial germ cells in culture

Development ◽  
1991 ◽  
Vol 113 (4) ◽  
pp. 1451-1457 ◽  
Author(s):  
I. Godin ◽  
C.C. Wylie

Primordial germ cells are the stem cells that provide the functional gametes of adult animals. In many animal groups they are set aside at the earliest stages of development, and migrate from their sites of first appearance to the sites where the gonad will form, the genital ridges. During this migration they proliferate. In the mouse embryo their numbers increase from less than one hundred to approximately four thousand during the period of their migration. In a previous paper we showed that both the proliferation and the direction of migration of mouse PGCs in culture were influenced by soluble factors released from their target tissue, the genital ridges. Studies on other stem cell populations have shown that complex combinations of growth factors control their proliferation, migration and differentiation. In this paper, we show that TGF beta 1 inhibits proliferation of PGCs taken from 8.5 day old embryos and cultured on embryonic fibroblast feeder layers. We also show that the previously reported chemotropic effect of genital ridges in this culture system is mediated by TGF beta 1, or a closely related molecule, released from the genital ridges.

Development ◽  
1991 ◽  
Vol 113 (4) ◽  
pp. 1365-1373 ◽  
Author(s):  
C. Ffrench-Constant ◽  
A. Hollingsworth ◽  
J. Heasman ◽  
C.C. Wylie

The adhesive extracellular matrix glycoprotein fibronectin is thought to play a central role in cell migration during embryogenesis. In order to define this role, we have examined the response to fibronectin in cell culture of mouse primordial germ cells (PGCs) before, during and after their migration from the hindgut into their target tissue, the genital ridges. Using an explant culture system, we show that PGCs will emigrate from tissue fragments containing hindgut, and that fibronectin stimulates this migration. Adhesion assays show that the start of PGC migration is associated with a fall in adhesion to fibronectin. Double-labelling studies using in situ hybridization and histochemistry demonstrate that migrating PGCs do not contain detectable fibronectin mRNA, suggesting that they do not synthesize and secrete the fibronectin within their migratory substratum. Taken together, these findings are consistent with an important role for fibronectin in stimulating PGC migration. In addition, however, they suggest that the interaction between PGCs and fibronectin may be important in timing the start of migration, with the fall in adhesion allowing the PGCs to commence their migration towards the genital ridges.


Biologicals ◽  
2017 ◽  
Vol 48 ◽  
pp. 114-120 ◽  
Author(s):  
Vahid Mansouri ◽  
Mohammad Salehi ◽  
Mir davood Omrani ◽  
Zahra Niknam ◽  
Abdolreza Ardeshirylajimi

Zoo Biology ◽  
2002 ◽  
Vol 21 (3) ◽  
pp. 287-294 ◽  
Author(s):  
Takaharu Kawashima ◽  
Rika Sakai ◽  
Koichiro Kano ◽  
Yoshinori Tamaki ◽  
Koichiro Hashimoto

2016 ◽  
Vol 113 (32) ◽  
pp. 9021-9026 ◽  
Author(s):  
Kanako Morohaku ◽  
Ren Tanimoto ◽  
Keisuke Sasaki ◽  
Ryouka Kawahara-Miki ◽  
Tomohiro Kono ◽  
...  

Reconstituting gametogenesis in vitro is a key goal for reproductive biology and regenerative medicine. Successful in vitro reconstitution of primordial germ cells and spermatogenesis has recently had a significant effect in the field. However, recapitulation of oogenesis in vitro remains unachieved. Here we demonstrate the first reconstitution, to our knowledge, of the entire process of mammalian oogenesis in vitro from primordial germ cells, using an estrogen-receptor antagonist that promotes normal follicle formation, which in turn is crucial for supporting oocyte growth. The fundamental events in oogenesis (i.e., meiosis, oocyte growth, and genomic imprinting) were reproduced in the culture system. The most rigorous evidence of the recapitulation of oogenesis was the birth of fertile offspring, with a maximum of seven pups obtained from a cultured gonad. Moreover, cryopreserved gonads yielded functional oocytes and offspring in this culture system. Thus, our in vitro system will enable both innovative approaches for a deeper understanding of oogenesis and a new avenue to create and preserve female germ cells.


2019 ◽  
Vol 123 ◽  
pp. 83-89 ◽  
Author(s):  
Long Xie ◽  
Zhenping Lu ◽  
Dongyang Chen ◽  
Mengmeng Yang ◽  
Yuying Liao ◽  
...  

2000 ◽  
Vol 79 (1) ◽  
pp. 80-85 ◽  
Author(s):  
L. Karagenç ◽  
J.N. Petitte

2017 ◽  
Vol 10 (1) ◽  
pp. 12-18
Author(s):  
Hui Xiong ◽  
Xiangchen Li ◽  
Qingyun Hu ◽  
Pengfei Hu ◽  
Weijun Guan

Stem cell technologies have been widely used in the study of spermatogenesis. However, deriving motile sperm from stem cells in vitro is still rarely achieved. We found that chicken primordial germ cells could directly differentiate into sperm by using retinoic acid in a non-testicular culture system. The induced sperms were characterised by RT-PCR, immunofluorescence and flow cytometry techniques. Results suggested that chicken primordial germ cells could produce motile sperm in vitro. Our work has provided a novel animal model of spermatogenesis in vitro, which might be used for male reproductive mechanism research.


2002 ◽  
Vol 48 (2) ◽  
pp. 143-150 ◽  
Author(s):  
Takaharu KAWASHIMA ◽  
Koichiro KANO ◽  
Yasuyuki KANNAN ◽  
Yoshinori TAMAKI ◽  
Koichiro HASHIMOTO

2012 ◽  
Vol 11 (13) ◽  
pp. 2196-2203 ◽  
Author(s):  
Ming-Cheng Chang ◽  
Jenn-Fa Liou ◽  
Jen-Wen Shiau ◽  
Jui-Jane Tailiu ◽  
Chein Tai ◽  
...  

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