Cell redundancy in the zona-intact preimplantation mouse blastocyst: a light and electron microscope study of dead cells and their fate

Development ◽  
1974 ◽  
Vol 31 (3) ◽  
pp. 643-654
Author(s):  
A. M. El-Shershaby ◽  
J. R. Hinchliffe

In the zona pellucida-intact 95 h post coitum mouse blastocyst, electron-microscopic studies reveal the presence, as a part of normal development, of 1–2 dead cells lying free on the surface of the inner cell mass (ICM) or trophoblast cells, and of 4–5 dead cells phagocytosed by 1CM cells. Such dead cells are electron-dense and show characteristic chromatopycnosis of the nucleus, and swelling of the endoplasmic reticulum. In addition, 1–2 digestive vacuoles with granular contents and myelin figures are found, principally in ICM cells, and corresponding with basophilic bodies observed with the light microscope. The results are interpreted as indicating that a relatively large number (i.e. a minimum of 6–8, or approximately 10%) of blastocyst cells die and are phagocytosed and digested, usually by the ICM cells, but probably also by trophoblast cells. This process does not, however, affect the future differentiation of the ingesting cell. Simultaneously a small number of epithelial cells adjacent to the blastocyst die, either singly or in small groups. These findings confirm the view that previous reports of penetration of the uterine epithelium by ‘primary invasive cells’ originating in the ICM were due to confusion between two separate groups of dead cells, namely the embryonic dead cells of the ICM and the single dead cells in the adjacent uterine epithelium, which appear to be phagocytosed by trophoblast cells following loss of the zona pellucida.

Development ◽  
1974 ◽  
Vol 32 (3) ◽  
pp. 675-695
Author(s):  
Mary Nadijcka ◽  
Nina Hillman

The mouse blastocyst stage covers approximately 2 days. During this period, embryonic development advances through four ultrastructurally distinct substages. Specific ultra-structural characteristics, such as changes in cell shape and/or the distribution of intracellular organelles, may be used to characterize the various cell types from each other at each substage (e.g. trophoblast from inner cell mass cells), as well as to distinguish the same cells from each other at different substages (e.g. substage 1 abembryonic trophoblast cells from substage 2 abembryonic trophoblast cells). A distinguishing characteristic of these blastocyst substages are the membrane contacts (tight junctions, desmosomes, focal tight junctions) between cells. The apical surfaces of adjacent trophoblast cells, from the time of cavity formation until the initial stage of implantation, are connected by a tight junction and a desmosome. The basal region of the apposed trophoblast membranes, however, vary both in their spatial interrelationship with each other and in their defined cellular contacts. Likewise, the cell contacts between the inner cell mass cells, and between these cells and the embryonic trophoblast cells, are distinctive for each blastocyst substage.


Development ◽  
1977 ◽  
Vol 39 (1) ◽  
pp. 273-277
Author(s):  
M. A. H. Surani ◽  
S. C. Barton

Preimplantation mouse blastocysts were dissected into inner cell mass (ICM) and trophoblast cells. These fragments were transferred to pseudo-pregnant mice which were left intact or ovariectomized. The latter group received progesterone to permit blastocysts and the dissected fragments to enter into quiescence, prior to injection of oestradiol to induce implantation. Trophoblastic vesicles, without ICM, entered into quiescence and implanted whereas the ICM did not. The entry of trophoblast into quiescence does not appear therefore to be governed by the ICM.


1995 ◽  
Vol 43 (1) ◽  
pp. 304 ◽  
Author(s):  
D. Rath ◽  
H. Niemann ◽  
T. Tao ◽  
M. Boerjan

Development ◽  
1982 ◽  
Vol 70 (1) ◽  
pp. 133-152
Author(s):  
Susan J. Kimber ◽  
M. Azim ◽  
H. Surani ◽  
Sheila C. Barton

Whole 8-cell morulae can be aggregated with isolated inner cell masses from blastocysts. On examining semithin light microscope sections of such aggregates we found that cells of the morula changed shape and spread over the surface of the ICM, thus translocating it to the inside of the aggregate. Using single cells from 8-cell embryos in combination with single cells from other stage embryos or isolated ICMs we show that 1/8 blastomeres spread over other cells providing a suitably adhesive surface. The incidence of spreading is high with inner cells from 16-cell embryos (56 %) and 32-cell embryos (62%) and isolated inner cell masses (64%). In contrast, the incidence of spreading of 1/8 blastomeres is low over outer cells from 16-cell embryos (26%) and 32-cell embryos (13%). Blastomeres from 8-cell embryos do not spread over unfertilized 1-cell eggs, 1/2 or 1/4 cells or trophectoderm cells contaminating isolated ICMs. When 1/8 cells are aggregated in pairs they flatten on one another (equal spreading) as occurs at compaction in whole 8-cell embryos. However, if 1/8 is allowed to divide to 2/16 in culture one of the cells engulfs the other (51-62/ pairs). Based on the ideas of Holtfreter (1943) and Steinberg (1964,1978) these results are interpreted to indicate an increase in adhesiveness at the 8-cell stage as well as cytoskeletal mobilization. Following the 8-cell stage there is an increase in adhesiveness of inside cells while the outside cells decrease in adhesiveness. The difference in adhesiveness between inside and outside cells in late morulae is probably central to the divergent differentiation of (inner) ICM and (outer) trophectoderm cell populations.


Development ◽  
1987 ◽  
Vol 100 (2) ◽  
pp. 325-332
Author(s):  
C.L. Garbutt ◽  
M.H. Johnson ◽  
M.A. George

Aggregate 8-cell embryos were constructed from four 2/8 pairs of blastomeres, one of which was marked with a short-term cell lineage marker and was also either 4 h older (derived from an early-dividing 4-cell) or 4 h younger (derived from a late-dividing 4-cell) than the other three pairs. The aggregate embryos were cultured to the 16-cell stage, at which time a second marker was used to label the outside cell population. The embryos were then disaggregated and each cell was examined to determine its labelling pattern. From this analysis, we calculated the relative contributions to the inside cell population of the 16-cell embryo of older and younger cells. Older cells were found to contribute preferentially. However, if the construction of the aggregate 8-cell embryo was delayed until each of the contributing 2/8 cell pairs had undergone intercellular flattening and then had been exposed to medium low in calcium to reverse this flattening immediately prior to aggregation, the advantage possessed by the older cells was lost. These results support the suggestion that older cells derived from early-dividing 4-cell blastomeres contribute preferentially to the inner cell mass as a result of being early-flattening cells.


Development ◽  
1977 ◽  
Vol 40 (1) ◽  
pp. 143-157
Author(s):  
Paul S. Burgoyne ◽  
Thomas Ducibella

Mouse embryos (8-cell to early blastocyst) were denuded with pronase, and apposed in pairs which represented a wide range of stage combinations. These pairs either formed aggregates which differentiated into double-sized blastocysts, or they failed to aggregate. The 8–16-cell stages would not envelop late morulae/early blastocysts to form layered aggregates. This must mean that as the embryo differentiates into a blastocyst, the outer surface of the trophoblast loses its capacity for supporting cell spreading. The aggregation data also demonstrate that embryos almost completely lose their potential for aggregation at a very discrete stage in development – namely, between 8 and 9 h before blastocoel formation. It is argued that this is the stage at which the zonular tight junctional seal is completed, and that it is this physical barrier which prevents aggregation. It has been argued previously that the zonular tight junctional seal allows the creation of the special microenvironment which is necessary for the determination of the inner cells as inner cell mass. The completion of this seal 8–9 h before it is required for the formation of a blastocoel would provide a suitable time period for this cell determination to occur. The results obtained also relate to the technique of chimera production. Since the aim of this technique is to generate mice with mixed cell populations, it is important that the blastocyst formed following aggregation should have both cell lines present in the inner cell mass. This can best be assured by using relatively late morula stages (75 h post-HCG injection) since these will have already segregated their inner cells, but the incomplete seal will still allow aggregation to take place.


Development ◽  
1995 ◽  
Vol 121 (5) ◽  
pp. 1333-1339 ◽  
Author(s):  
P. Bhatnagar ◽  
V.E. Papaioannou ◽  
J.D. Biggers

The effects of macrophage colony stimulating factor on the development of the zygote to the blastocyst stage of an outbred strain of mouse have been studied in KSOM, an improved medium that supports a high rate of in vitro development. Macrophage colony stimulating factor accelerates the formation of the blastocyst cavity by day 4 (96 hours post-hCG). It also increases overall embryonic cell number through a differential increase in the number of trophoblast cells, with no significant effect on the number of inner cell mass cells. By day 5 of culture (120 hours post-hCG), colony stimulating factor-treated embryos have about 20 more trophoblast cells than control embryos, an increase of about 30 percent of the total number of cells in a control blastocyst. The maximum response of embryos was obtained at a concentration around 540 U ml-1 colony stimulating factor (identical to 918 Stanley units ml-1), and the cytokine can produce the same effects even if it is present in the medium for only part of the culture period. This in vitro stimulation of preimplantation development with macrophage colony stimulating factor is compatible with continued normal fetal development in vivo.


Development ◽  
1975 ◽  
Vol 33 (4) ◽  
pp. 979-990
Author(s):  
J. Rossant

Inner cell masses (ICMs) were dissected from 3½- and 4½-day blastocysts and cultured in contact with 2½-day morulae. Blastocysts and morulae were homozygous for different electrophoretic variants of the enzyme glucose phosphate isomerase (GPI). Aggregation of ICMs and morulae was observed, and such aggregates were able to form blastocysts in vitro and morphologically normal foetuses in utero. GPI analysis of these conceptuses revealed that most were chimaeric. However, donor ICM-type isozyme was only detected in the embryonic and extra-embryonic fractions of the chimaeras and never in the trophoblastic fraction. Thus, ICM cells appear unable to form trophoblast derivatives even when exposed to ‘outside’ conditions as experienced by developing trophoblast cells. This is evidence that ICM cells, although not overtly differentiated, are determined by 3½ days.


Development ◽  
1978 ◽  
Vol 48 (1) ◽  
pp. 53-72
Author(s):  
C. F. Graham ◽  
Z. A. Deussen

The cell lineage of the mouse was studied from the 2-cell stage to the blastocyst. Lineage to the 8-cell stage was followed under the microscope. Each cell from the 2-cell stage divided to form two daughter cells which remained attached. Subsequently, these two daughters each produced two descendants; one of these descendants regularly lay deep in the structure of the embryo while the other was peripheral. Lineage to the blastocyst was followed by injecting oil drops into cells at the 8-cell stage, and then following the segregation of these drops into the inner cell mass and trophectoderm. Between the 8-cell stage and the blastocyst, the deep cells contributed more frequently to the inner cell mass than did the peripheral cells.


2017 ◽  
Vol 41 (5) ◽  
pp. 496-510.e5 ◽  
Author(s):  
Minjung Kang ◽  
Vidur Garg ◽  
Anna-Katerina Hadjantonakis

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