The primordial germ cells in early mouse embryos: Light and electron microscopic studies

1973 ◽  
Vol 31 (2) ◽  
pp. 275-284 ◽  
Author(s):  
Kwang W. Jeon ◽  
John R. Kennedy
Development ◽  
1978 ◽  
Vol 46 (1) ◽  
pp. 119-133
Author(s):  
Janet Heasman ◽  
C. C. Wylie

Primordial germ cells (PGCs) of Xenopus laevis have been isolated from early embryos and kept alive in vitro, in order to study the structural basis of their motility, using the transmission and scanning electron microscope. The culture conditions used mimicked as closely as possible the in vivo environment of migrating PGCs, in that isolated PGCs were seeded onto monolayers of amphibian mesentery cells. In these conditions we have demonstrated that: (a) No significant differences were found between the morphology of PGCs in vitro and in vivo. (b) Structural features involved in PGC movement in vitro include (i) the presence of a filamentous substructure, (ii) filopodial and blunt cell processes, (iii) cell surface specializations. These features are also characteristic of migratory PGCs studied in vivo. (c) PGCs in vitro have powers of invasion similar to those of migrating PGCs in vivo. They occasionally become completely surrounded by cells of the monolayer and, in this situation, bear striking resemblance to PGCs moving between mesentery cells to the site of the developing gonad in stage-44 tadpoles. We conclude that as far as it is possible to assess, the behaviour of isolated PGCs in these in vitro conditions mimics their activities in vivo. This allows us to study the ultrastructural basis of their migration.


1979 ◽  
Vol 21 (1) ◽  
pp. 3-10 ◽  
Author(s):  
TOYOAKI FUJIMOTO ◽  
ATSUMI UKESHIMA ◽  
YUKIHIKO MIYAYAMA ◽  
FUMIYO HORIO ◽  
ETSUKO NINOMIYA

2014 ◽  
Vol 385 (2) ◽  
pp. 155-159 ◽  
Author(s):  
Harry G. Leitch ◽  
Daiji Okamura ◽  
Gabriela Durcova-Hills ◽  
Colin L. Stewart ◽  
Richard L. Gardner ◽  
...  

Development ◽  
1973 ◽  
Vol 30 (1) ◽  
pp. 97-118
Author(s):  
Martha Spiegelman ◽  
Dorothea Bennett

The primordial germ cells (PGC's) of the early mouse embryo have been identified in semi-thin and ultra-thin plastic sections on the combined bases of location and a distinctive set of morphological features. These cells originate extra-gonadally and their path of migration during the stages investigated agrees with results of previous histological and experimental studies. At 8–9 days of development, PGC's are observed among the endoderm cells of the mid- and hindgut and the yolk stalk; at 10–11 days, PGC's are seen in the dorsal mesentery, the dorsal coelomic lining, and in the rudimentary genital ridge; by 13 days, the gonad is abundantly populated with germ cells. During the migratory period the PGC's appear as small (10–12 μm diameter), oval, basophilic cells which have a large nucleo-cytoplasmic ratio. These cells possess numerous free ribosomes and polysomes, a filamentous ground cytoplasm, and few profiles of endoplasmic reticulum. Mitochondria display small oval and thread-like profiles. A Golgi complex is not prominent in the PGC's. The densely granular and fibrillar nucleus is often oval in outline but sometimes shows irregular contours. A large nucleolus is present. Although located among groups of cells that exhibit extensive cell junctions, the PGC's have not been found to share such junctions with neighboring cells. Furthermore, the PGC's possess small cytoplasmic processes that contain numerous microfilaments. These observations are interpreted as morphological correlates to the migratory activity of these cells. In the early PGC's located in the gut, regions of the endoplasmic reticulum where membranes are closely apposed, perhaps fused, often present the appearance of annulate cisternae. In addition, compact aggregates of granulofibrillar material are found in the cytoplasm of these same cells. Neither of these structures is detected in the mesenteric PGC's, the gonadal germ cells, or any other cell of the embryo at the stages studied. It is suggested that these two cytoplasmic elements may be related to further differentiation of the germ cells. The germ cells of the developing gonad are large, oval cells which possess a nucleus of very round contour. Both the nucleus and the cytoplasm retain a densely granular appearance. The expanded cytoplasm contains a large Golgi complex but still few profiles of endoplasmic reticulum. Free ribosomes and polysomes are abundant. The germ cells share extensive gap junctions with one another and with adjacent stromal cells.


Development ◽  
1990 ◽  
Vol 109 (4) ◽  
pp. 911-923 ◽  
Author(s):  
A. Orr-Urtreger ◽  
A. Avivi ◽  
Y. Zimmer ◽  
D. Givol ◽  
Y. Yarden ◽  
...  

Developmental expression of the c-kit proto-oncogene, a receptor tyrosine kinase encoded by the W locus, was investigated by in situ hybridization in normal mouse embryos. Early after implantation transcripts were detectable only in the maternal placenta (6 1/2-7 1/2 days p.c.). Subsequently (8 1/2 days p.c.) numerous ectodermal (neural tube, sensory placodes) and endodermal (embryonic gut) derivatives expressed c-kit. Later transcripts were detected also in the blood islands of the yolk sac and in the embryonic liver, the main sites of embryonic hemopoiesis. Around midgestation, transcripts accumulated in the branchial pouches and also in primordial germ cells of the genital ridges. This complex pattern of expression remained characteristic also later in gestation, when c-kit was expressed in highly differentiated structures of the craniofacial area, in presumptive melanoblasts and in the CNS. In the adult ovary, maternal c-kit transcripts were detected. They were present in the oocytes of both immature and mature ovarian follicles, but not in the male germ line, where c-kit expression may be down regulated. Thus, c-kit activity is complex and appears in multiple tissues including those that also display defects in mutations at the W locus where c-kit is encoded. Correlation between W phenotypes and c-kit expression, as well as the regulation of the complex and multiple expression of polypeptide growth factors and receptors, is discussed.


Reproduction ◽  
2016 ◽  
Vol 151 (1) ◽  
pp. 51-58 ◽  
Author(s):  
Eunsook Park ◽  
Bobae Lee ◽  
Bruce E Clurman ◽  
Keesook Lee

Nucleoporin 50 kDa (NUP50), a component of the nuclear pore complex, is highly expressed in male germ cells, but its role in germ cells is largely unknown. In this study, we analyzed the expression and function of NUP50 during the embryonic development of germ cells using NUP50-deficient mice. NUP50 was expressed in germ cells of both sexes at embryonic day 15.5 (E15.5), E13.5, and E12.5. In addition, NUP50 expression was also detected in primordial germ cells (PGCs) migrating into the genital ridges at E9.5. The gonads of Nup50−/− embryos of both sexes contained few PGCs at both E11.5 and E12.5 and no developing germ cells at E15.5. The migratory PGCs in Nup50−/− embryos at E9.5 showed increased apoptosis but a normal rate of proliferation, resulting in the progressive loss of germ cells at later stages. Taken together, these results suggest that NUP50 plays an essential role in the survival of PGCs during embryonic development.


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