Theoretical exploration of blastocyst morphogenesis.
نویسندگان
چکیده
A theoretical exploration of cell distribution on the mouse blastocyst is conducted. A model ball of cells represents the morula which develops into a 32-cell model blastocyst that is enclosed in a spherical surface with a hemispherical cavity at one end. In the combinatorial analysis it is assumed that each cell of the 2-cell embryo forms 16 cells in the blastocyst and that these 16 cells touch each other. The results of the analysis identify a tendency for one set of 16 cells to contribute twice as many cells to the basal solid end of the blastocyst than the other set, a developmental bias that is also found by some observers of natural blastocysts. In the geometric analysis, half the volume of the inner group of cells of the morula and blastocyst and half the volume of the surrounding shell cells, the trophectoderm, is assumed to be formed from the progeny of each 2-cell stage cell. Making various assumptions about morphogenesis, it is found that there is a tendency for a curved frontier between the volumes from each 2-cell stage cell, the clonal volumes, to lie at an angle of 43.4 degrees to the equator of the blastocyst and for the bulk of the frontier circumference to lie on either side of the equator. These tendencies are also found by some observers of real blastocysts.
منابع مشابه
Morphogenesis of the mammalian blastocyst.
The first 4 days of mouse pre-implantation development are characterized by a period of segmentation, including morphogenetic events that are required for the divergence of embryonic and extra-embryonic lineages. These extra-embryonic tissues are essential for the implantation into the maternal uterus and for the development of the foetus. In this review, we first discuss data showing unambiguo...
متن کاملCell adhesion in the preimplantation mammalian embryo and its role in trophectoderm differentiation and blastocyst morphogenesis.
Cell adhesion plays a critical role in the differentiation of the trophectoderm epithelium and the morphogenesis of the blastocyst. In the mouse embryo, E-cadherin mediated adhesion initiates at compaction at the 8-cell stage, regulated post-translationally via protein kinase C and other signalling molecules. E-cadherin adhesion organises epithelial polarisation of blastomeres at compaction. Su...
متن کاملRole of the Mitochondrial Genome during Early Development in Mice
The role of the mitochondrial genome in early development and differentiation was studied in mouse embryos cultured in vitro from the two to four cell stage to the blastocyst (about 100 cells). During this period the mitochondria undergo morphological differentiation: progressive enlargement followed by an increase in matrix density, in number of cristae, and in number of mitochondrial ribosome...
متن کاملROLE OF THE MITOCHONDRIAL GENOME DURING EARLY DEVELOPMENT IN MICE Effects of Ethidium Bromide and Chloramphenicol
The role of the mitochondrial genome in early development and differentiation was studied in mouse embryos cultured in vitro from the two to four cell stage to the blastocyst (about 100 cells). During this period the mitochondria undergo morphological differentiation : progressive enlargement followed by an increase in matrix density, in number of cristae, and in number of mitochondrial ribosom...
متن کاملA Role for Borg5 During Trophectoderm Differentiation
Stem cell differentiation is accompanied by a gradual cellular morphogenesis and transcriptional changes. Identification of morphological regulators that control cell behavior during differentiation could shed light on how cell morphogenesis is coupled to transcriptional changes during development. By analyzing cellular behavior during differentiation of mouse embryonic stem cells (ESCs), we un...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The International journal of developmental biology
دوره 53 4 شماره
صفحات -
تاریخ انتشار 2009