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Experimental Embryology

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Experimental embryology, a branch of embryology, is an important partner of descriptive embryology. Hypotheses about development are tested using genetic and embryo manipulations, e.g., lesions, transplantations, and transgenic organisms. Important concepts developed by experimental embryologists include induction, commitment, and programmed cell death. Experimental embryology addresses, for example, questions about mechanisms underlying observed developmental changes, including whether these changes are autonomous or conditional.


Contents

Cell-autonomous (or mosaic) Development

Observation of development in undisturbed embryos gives the impression that cells follow a genetic program to their cell fate, perhaps influenced by the portion of cytoplasm it inherited during cleavage. A cell's fate is thus largely determined by its lineage (Sidney Brenner's "European plan").

  • Ablation of one or more blastomeres may result in missing parts.
  • Transplanted cells may develop as if they had not been moved.
  • This type of development is thought to be important in most invertebrates.

Conditional (or regulative) Development

Manipulation of embryos often demonstrates that cell fate is influenced by the cell's environment. Cellular behavior may be influenced by intercellular signaling molecules (e.g., morphogens), direct cell-cell interactions (e.g., via cell-adhesion molecules) and extracellular matrix. A cell's fate is thus largely determined by its neighbors (Brenner's "American plan").

  • Ablation of one or more blastomeres may have little effect on the final form of the organism.
  • Transplanted cells may develop differently, or influence the development of its new neighbors.
  • This type of development is thought to be important in vertebrates and some invertebrates (including most insects).

Induction

Induction is the influence of an inductor (an "organizer" or "evocator") on the differentiation of adjacent cells or the development of an embryonic structure. Differentiation under the influence of an organizer or other "positional information" is an important component of theories of pattern formation in morphogenesis.
An organizer is a group of cells that influence the growth and development of adjacent (competent) cells, through the effects of an evocator.

Competence

Competence is the ability of a cell to respond in a specific manner to an inductor. For example, competence may depend on the expression of a specific cell-surface receptor for an evocator.

Experimental Approaches

Hans Spemann received a Nobel Prize in 1935 for discovery of the organizer effect in embryonic development.

  • Organizers are traditionally characterized by the effects of their ablation on surrounding tissues, or the effects of their transplantation on surrounding host tissues.
  • Tests of potential evocators include injection into embryos and studies of transgenic mice.

Commitment

Differentiation is an overt change in cellular biochemistry, structure and function. It is preceded by the covert commitment of cells to particular fates. Commitment is divided into two stages, specification and determination. Specification are early, reversible steps; whereas determination implies irreversibility.

Potential

Potency is the extent of the potential of a developing cell to differentiate into a variety of cell types. During development, the potency of cells is generally reduced as they become differentiated. Potency and commitment have an inverse relationship. The prospective potency of an embryonic cell (the set of cell types that could arise from it) is greater than its prospective fate (the set of cell types that would be produced in normal, unaltered development).

  • Embryonic stem cells are totipotential cells (able to differentiate into any type of cell).
  • Most stem cells are pluripotential cells (able to differentiate into many cell types).
  • Progenitor cells include multipotential cells (able to differentiate into several cell types) and committed cells.

Experimental Approaches

The standard experiments to test cellular commitment and potential include transplantation and ablation.

  • Tissues can be destroyed to determine if there are any changes in the differentiation of tissues surrounding the lesion.
  • Tissues can be moved to a different location (in the same or a different individual) to test their commitment and potential, and to examine the effects of graft and host tissues on each other.

Programmed Cell Death (Apoptosis)

Perhaps surprisingly, cell death is a normal developmental (morphogenetic) process. If cells are no longer needed, they commit suicide by activating an intracellular death program, called programmed cell death or apoptosis. Well studied examples of apotosis in normal vertebrate development include:

  • Sculpting the digits in the developing mouse paw by apoptosis. Interdigital tissue between digital rays in the paw plate is removed by apoptosis, probably induced by bone morphogenetic proteins.
  • In the frog spinal cord, more neurons are produced than are needed. This strategy of overproduction followed by culling ensures that all target cells are contacted by nerve cells and that extra nerve cells are eliminated.

Growth factors

Cell survival may be dependent upon the presence of growth factors. For example, survival of spinal cord motor neurons depends on nerve growth factor released by their target cells (muscle cells). Growth factors are also important inducers of proliferation and differentiation.

Experimental approaches

  • John Sulston shared a Nobel Prize in 2002 for his description of cell lineage in development of the nematode worm C. elegans. He described the pattern of cell proliferation that resulted in adults containing exactly 959 cells, and found that during development another 131 cells died.
  • H. Robert Horvitz shared a Nobel Prize in 2002 for his work on genetic analysis of programmed cell death in development of C. elegans. He discovered and characterized genes involved in programmed cell death in C. elegans, and showed that similar genes are present in humans.
  • Stanley Cohen and Rita Levi-Montalcini shared a Nobel Prize in 1986 for the discovery and and isolation of growth factors (Nerve growth factor and Epidermal growth factor).

History

Nobel Prizes

Several Nobel Prizes in Medicine and Physiology have recognized work in experimental embryology.

Year Awardee(s) Citation Organism(s)
1933 Thomas Hunt Morgan "for his discoveries concerning the role played by the chromosome in heredity" Drosophila
1935 Hans Spemann "for his discovery of the organizer effect in embryonic development" amphibians
1986 Stanley Cohen & Rita Levi-Montalcini "for their discoveries of growth factors" mouse and chick
1995 Edward B. Lewis, Christianne ~Nüsslein-Volhard & Eric F. Wieschaus "for their discoveries concerning the genetic control of early embryonic development" Drosophila
2001 R. Timothy Hunt, Leland H. Hartwell & Paul M. Nurse "for their discoveries of key regulators of the cell cycle" sea urchin (Hunt) and yeast (Hartwell & Nurse)
2002 Sidney Brenner, H. Robert Horvitz & John E. Sulston "for their discoveries concerning genetic regulation of organ development and programmed cell death" C.elegans
2007 Mario Capecchi, Martin Evans & Oliver Smithies "for their discoveries for introducing specific gene modifications in mice by the use of embryonic stem cells" mouse

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The content on or accessible through Medpedia.com is for informational purposes only. Medpedia is not a substitute for professional advice or expert medical services from a qualified health professional. Read more

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