Cell fate determination

Within the field of developmental biology, one goal is to understand how a particular cell develops into a final cell type, known as fate determination. Within an embryo, several processes play out at the cellular and tissue level to create an organism. These processes include cell proliferation, differentiation, cellular movement[1] and programmed cell death.[2][3] Each cell in an embryo receives molecular signals from neighboring cells in the form of proteins, RNAs and even surface interactions. Almost all animals undergo a similar sequence of events during very early development, a conserved process known as embryogenesis.[4] During embryogenesis, cells exist in three germ layers, and undergo gastrulation. While embryogenesis has been studied for more than a century, it was only recently (the past 25 years or so) that scientists discovered that a basic set of the same proteins and mRNAs are involved in embryogenesis. Evolutionary conservation is one of the reasons that model systems such as the fly (Drosophila melanogaster), the mouse (Mus musculus), and other organisms are used as models to study embryogenesis and developmental biology. Studying model organisms provides information relevant to other animals, including humans. While studying the different model systems, cells fate was discovered to be determined via multiple ways, two of which are by the combination of transcription factors the cells have and by the cell-cell interaction.[5] Cells' fate determination mechanisms were categorized into three different types, autonomously specified cells, conditionally specified cells, or syncytial specified cells. Furthermore, the cells' fate was determined mainly using two types of experiments, cell ablation and transplantation.[6] The results obtained from these experiments, helped in identifying the fate of the examined cells.

  1. ^ Wallingford, John B; Fraser, Scott E; Harland, Richard M (2002-06-01). "Convergent Extension: The Molecular Control of Polarized Cell Movement during Embryonic Development". Developmental Cell. 2 (6): 695–706. doi:10.1016/S1534-5807(02)00197-1. ISSN 1534-5807. PMID 12062082.
  2. ^ Miura, Masayuki; Yamaguchi, Yoshifumi (2015-02-23). "Programmed Cell Death in Neurodevelopment". Developmental Cell. 32 (4): 478–490. doi:10.1016/j.devcel.2015.01.019. ISSN 1534-5807. PMID 25710534.
  3. ^ Ranganath, R. M.; Nagashree, N. R. (2001). "Role of programmed cell death in development". International Review of Cytology. 202: 159–242. doi:10.1016/s0074-7696(01)02005-8. ISBN 9780123646064. ISSN 0074-7696. PMID 11061565.
  4. ^ Saenko, SV; French, V; Brakefield, PM; Beldade, P (27 April 2008). "Conserved developmental processes and the formation of evolutionary novelties: examples from butterfly wings". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 363 (1496): 1549–55. doi:10.1098/rstb.2007.2245. PMC 2615821. PMID 18192179.
  5. ^ Streuli, Charles H. (2009-01-15). "Integrins and cell-fate determination". Journal of Cell Science. 122 (2): 171–177. doi:10.1242/jcs.018945. ISSN 0021-9533. PMC 2714415. PMID 19118209.
  6. ^ Featherstone, D. E.; Broadie, K. S. (2005-01-01), Gilbert, Lawrence I. (ed.), "2.3 - Functional Development of the Neuromusculature", Comprehensive Molecular Insect Science, Amsterdam: Elsevier, pp. 85–134, ISBN 978-0-444-51924-5, retrieved 2021-03-22

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