Oogonium
Oogonium | |
---|---|
Identifiers | |
MeSH | D009867 |
FMA | 83673 |
Anatomical terminology |
An oogonium (pl.: oogonia) is a small
In the mammalian fetus
Oogonia are formed in large numbers by mitosis early in fetal development from primordial germ cells. In humans they start to develop between weeks 4 and 8 and are present in the fetus between weeks 5 and 30.
Structure
Normal oogonia in human
The
Oogonia that are undergoing degeneration appear slightly different under the electron microscope. In these oogonia, the chromosomes clump together into an indistinguishable mass within the nucleus and the mitochondria and E.R. appear to be swollen and disrupted. Degenerating oogonia are usually found partially or wholly engulfed in neighboring somatic cells, identifying phagocytosis as the mode of elimination.[1]
Development and differentiation
In the blastocyst of the mammalian embryo, primordial germ cells arise from proximal epiblasts under the influence of extra-embryonic signals. These germ cells then travel, via amoeboid movement, to the genital ridge and eventually into the undifferentiated gonads of the fetus.[2] During the 4th or 5th week of development, the gonads begin to differentiate. In the absence of the Y chromosome, the gonads will differentiate into ovaries. As the ovaries differentiate, ingrowths called cortical cords develop. This is where the primordial germ cells collect.[3][4]
During the 6th to 8th week of female (XX) embryonic development, the primordial germ cells grow and begin to differentiate into oogonia. Oogonia proliferate via mitosis during the 9th to 22nd week of embryonic development. There can be up to 600,000 oogonia by the 8th week of development and up to 7,000,000 by the 5th month.[3]
Eventually, the oogonia will either degenerate or further differentiate into primary oocytes through asymmetric division. Asymmetric division is a process of mitosis in which one oogonium divides unequally to produce one daughter cell that will eventually become an oocyte through the process of oogenesis, and one daughter cell that is an identical oogonium to the parent cell. This occurs during the 15th week to the 7th month of embryonic development.[2] Most oogonia have either degenerated or differentiated into primary oocytes by birth.[3][5]
Primary oocytes will undergo oogenesis in which they enter meiosis. However, primary oocytes are arrested in prophase 1 of the first meiosis and remain in that arrested stage until puberty begins in the female adult.[6] This is in contrast to male primordial germ cells which are arrested in the spermatogonial stage at birth and do not enter into spermatogenesis and meiosis to produce primary spermatocytes until puberty in the adult male.[3]
Regulation of oogonia differentiation and entry into oogenesis
The regulation and differentiation of germ cells into primary
After female (XX) germ cells collect in the undifferentiated gonads, the up-regulation of Stra8 is required for germ cell differentiation into an oogonium and eventually enter meiosis. One major factor that contributes to the up-regulation of Stra8, is the initiation of the β-Catenin signaling pathway via RSPO1, which is also responsible for ovary differentiation. Since RSPO1 is produced in somatic cells, this protein acts on germ cells in a
Oogonial stem cells
It is theorized that oogonia either degenerate or differentiate into
Recent research, however, has identified that renewable oogonia may be present in the lining of the female ovaries of humans, primates and mice.[2][7][8] It is thought that these germ cells might be necessary for the upkeep of the reproductive follicles and oocyte development, well into adulthood. It has also been discovered that some stem cells may migrate from the bone marrow to the ovaries as a source of extra-genial germ cells. These mitotically active germ cells found in mammalian adults were identified by tracking several markers that were common in oocytes. These potential renewable germ cells were identified as positive for these essential oocyte markers.[2]
The discovery of these active germ cells and oogonia in the adult female could be very useful in the advancement of fertility research and treatment of infertility.[2][8] Germ cells have been extracted, isolated and grown successfully in vitro.[8] These germ cells have been used to restore fertility in mice by promoting follicle generation and upkeep in previously infertile mice. There is also research being done on possible germ line regeneration in primates. Mitotically active human female germ cells could be very beneficial to a new method of embryonic stem cell development that involves a nuclear transfer into a zygote. Using these functional oogonia may help to create patient-specific stem cell lines using this method.[2]
Controversy
There is a significant controversy regarding existence of mammalian oogonial stem cells. The controversy lies in negative data that has originated from many laboratories in the United States. Multiple approaches to verify the existence of oogonial stem cells have yielded negative results, and no research group in United States has been able to reproduce initial findings.[9][10][11]
In certain thallophytes
In phycology and mycology, oogonium refers to a female gametangium if the union of the male (motile or non-motile) and the female gamete takes place within this structure.[12][13]
In
In many algae (e.g.,
Structure
The oogonia of certain Thallophyte species[
In
Fertilization
In a common mode of fertilization found in certain species of Thallophytes, the antheridia will bind with the oogonia. The antheridia will then form fertilization tubes connecting the antheridial cytoplasm with each oosphere within the oogonia. A haploid nucleus (gamete) from the antheridium will then be transferred through the fertilization tube into the oosphere, and fuse with the oosphere's haploid nucleus forming a diploid oospore. The oospore is then ready to germinate and develop into an adult diploid somatic stage.[14]
See also
List of distinct cell types in the adult human body
References
- ^ PMID 4933750. Archived from the originalon 4 March 2016. Retrieved 6 April 2012.
- ^ a b c d e f g h "Germ Stem Cells, A Scientific Summary". New Jersey Medical School. Archived from the original on 12 January 2012. Retrieved 6 April 2012.
- ^ ISBN 0-12-389775-0.
- ^ PMID 21991325.
- ^ "Human Emryology, Embryogenesis". Module 3, Gametogenesis. Retrieved 6 April 2012.
- ^ "Genetics, Meiosis and Gaetogenesis". www.emich.edu. Archived from the original on 30 April 2012. Retrieved 6 April 2012.
- S2CID 1289213.
- ^ PMID 22366948.
- S2CID 2949653.
- PMID 23630252.
- PMID 28389520.
- ISBN 0-7992-1793-X
- ^ Smyth, G.M. 1955. Cryptogamic Botany. vol. 1. McGraw-Hill Book Company
- ^ a b c d "Sexual Sporulation in Oomycota". Archived from the original on 12 April 2012. Retrieved 6 April 2012.