Introduction
Cleavage of the Zygote forms 2 blastomeres, cleavage with no cytoplasm synthesis, therefore individual cell volume decreases (More? embryonic cell cycle).

2 Blastomeres
(More? see quicktime movie of early cell division)
The zygote divides and develops into a solid ball of cells, the morulla, so called because of its mulberry-like appearance.
Cell division is initially synchronous, then asynchronous (slow- centre cells, larger fast- peripheral
cells, flattened against zona pellucida). The solid ball of cells undergoes
compaction (day 3-4) and then a cavity begins to form inside the ball, this whole
structure becomes the blastocyst (day 5).
The blastocyst has 2 cell populations: an inner cell mass (which will form
the entire embryo) and a shell of cells (cytotrophoblastic shell, which
will form the placenta). From the blastocyst stage onward different
populations of cells begin to be established.
Human embryo- in vitro blastocyst formation
Timecourse: Fertilization, Day 2-5 cell division, Day 5 cell compaction, early and
late cavitation, early blastocyst, expanding blastocyst.
(Modified from Fong and Bongso, Human Reproduction 1999 |
see also images of in vitro blastocyst formation)
Some Recent Findings
Recent review by Chen HW, Chen JJ, Yu SL, Li HN, Yang PC, Su CM, Au HK, Chang CW, Chien LW, Chen CS, Tzeng CR.
Transcriptome analysis in blastocyst hatching by cDNA microarray.
Hum Reprod. 2005 Sep;20(9):2492-501.
A microarray study of hatching specific genes in the mouse blastocyst showing high expression of adhesion and migration molecues required for
blastocyst attachment and altered levels in delayed growth embryos. They also demonstrated corresponding strong and specific immunostaining of
E-cadherin and NCAM in hatched blastocysts.
Hatching specific genes include:
- cell adhesion and migration molecules - E-cadherin, neuronal cell adhesion molecule (NCAM), lectin, galactose binding, soluble 7 (Lgals7), vanin 3, biglycan
- epigenetic regulators - Dnmt1, SIN3 yeast homolog A
- stress response regulators - Dnmt1, SIN3 yeast homolog A
- immunoresponse regulators - interleukin (IL)-2-inducible T-cell kinase, IL-4R, interferon- receptor 2, neurotrophin
Embryonic Cell Cycle
These early embryonic cell cycles differ by having little or no intervening growth phases simply Mitosis and DNA replication.
Embryonic cell cycle: Cell Division (Mitosis, M Phase) - DNA synthesis (S Phase) Cell Division (Mitosis, M Phase) - DNA synthesis (S Phase)
Normal cell cycle: Cell Division (Mitosis, M Phase) - Growth Phase 1 (G1 Phase) - DNA synthesis (S Phase) Growth Phase 2 (G2 Phase) - (Mitosis, M Phase)
(More? Mitosis)
References
Links: Journals | Online Textbooks | Search Textbooks | PubMed |
Search PubMed | Glossary
PubMed
Reviews
Lynn Lamoreux M, Kelsh RN, Wakamatsu Y, Ozato K.
Pigment pattern formation in the medaka embryo. Pigment Cell Res. 2005 Apr;18(2):64-73.
Articles
Chen HW, Chen JJ, Yu SL, Li HN, Yang PC, Su CM, Au HK, Chang CW, Chien LW, Chen CS, Tzeng CR.
Transcriptome analysis in blastocyst hatching by cDNA microarray.
Hum Reprod. 2005 Sep;20(9):2492-501.
Old References from 1999:
- Expression of Fgfr2 in the early mouse
embryo indicates its involvement in
preimplantation development. Haffner-Krausz
R, Gorivodsky M, Chen Y, Lonai P Mech
Dev 1999 Jul 1;85(1-2):167-172
- "We report that the IIIc transcriptional
alternative of Fgfr2 is transcribed in the
unfertilized egg and that during early
zygotic transcription, messages encoded by
both Fgfr2 alternatives (IIIc and IIIb) are
present. The Fgfr2 protein was first detected
in peripheral blastomeres of compacted
morulae. Trophectoderm specificity of Fgfr2
became obvious in the early blastocyst and
with maturation its localization underwent
further specification, Fgfr2 concentration
increased at the abembryonic pole and
decreased at the embryonic pole. Moreover
Fgfr2 expression became markedly asymmetrical
along the animal-vegetal axis of the mature
blastocyst. Our observations indicate a role
for Fgfr2 in trophectoderm growth and
specification and in the orientation and
polarity of the preimplantation
conceptus."
- Development of cellular polarity of
hamster embryos during compaction. Suzuki H,
Azuma T, Koyama H, Yang X Biol Reprod 1999
Aug;61(2):521-6
- "Development of cellular polarity is an
important event during early mammalian embryo
development and differentiation. Blastomeres
of hamster embryos at various stages were
examined by scanning electron microscopy
(SEM) and immunocytochemical staining. SEM
observations revealed that 1- to 7-cell-stage
embryos showed a uniform distribution of
microvilli throughout the cell surface.
Microvillous polarization was initially noted
in the blastomeres (10-35%) of 8-cell-stage
embryos. The polarized microvilli were
observed mostly in the basal region of
cell-cell contact and occasionally at the
apical, outward-facing surface of the
blastomere.
Fluorescein-isothiocyanate-conjugated
concanavalin A failed to reveal any polarity
in the blastomeres regardless of the stages
of the embryos. Actin staining showed that
microfilaments were present beneath the cell
surface, and in addition, areas of cell
contact were more heavily stained, indicating
a thick microfilament domain. Microtubules
were located throughout the cytoplasm and
were heavily concentrated near the nucleus
during interphase, although they became
redistributed in the region of the mitotic
spindle during karyokinesis. The position of
nucleus changed from the cell center to the
apical, outward-facing surface of the cell,
and it distanced itself from the basal
microvillous pole. It is suggested that the
changes in the cell surface and nuclear
position are the first manifestations of cell
polarity in peri-compacted hamster embryos,
which appear as early as the 8-cell stage;
furthermore, the outward migration of the
nuclei may parallel the redistribution of
microtubules in the cytoplasm."
Search PubMed
Search May 2006 "blastocyst development" 8,126 reference articles of which 790 were reviews.
Search PubMed Now: term = blastocyst+development
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