Embryology of the Face 2

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    EMBRYOLOGY OF THE FACE

    INTRODUCTION

    Human being comes into existence

    as single fertilized ovum cell.

    Fertilization involves the fusion of

    the male and female gem cells (i.e.Spermatozoa and Ova) to form a

    Zygote, which commences the

    formation of a new individual. Pre-

    natal development occupies 10-lunar

    months. Pre-natal development isdivided into 3 successive phases.

    The 1st 2 phases can be combined to

    constitute the Embryonic stage of

    development.

    The 3rd phase is called the fetal

    stage. The forming individual can be

    described as an Embryo or Fetus

    depending on its developmental

    stage.

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    1ST phase begins at fertilization and

    spans the first 4 weeks of the

    development. This phase involveslargely cellular proliferation and

    migration with some differentiation

    of cell populations.

    Few congenital defects can resultfrom this period of development

    because, if the disturbance is severe,

    the embryo is lost but if it is less

    severe the proliferative response can

    compensate by a process of cellrenewal.

    The second phase spans the next 4

    weeks of development and it is

    largely characterized by the

    differentiation of all major externaland internal structures

    (morphogenesis).

    This is a particularly vulnerable

    period of development for the

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    embryo because it involves many

    intricate embryologic processes and

    it is during this period that manyrecognized congenital defects

    develop.

    From the end of the second phase to

    third, further development is largelya matter of growth and maturation

    and the embryo is now called fetus.

    INDUCTION, COMPETENCE

    AND DIFFERENTIATIONThese terms, induction, competence

    and differentiation, describe

    important concepts in Embryology.

    All the cells of an individual stem

    from the Zygote. These cells clearlydifferentiate into populations that

    assume particular functions, shapes

    and rates of turn over. These

    populations of cells are said to be

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    compartmentalized such that

    successive generation of cells in a

    given compartment may eitherremain constant or differentiate i.

    e. change their characteristics and

    establish a new population of cells.

    The process that initiatesdifferentiation is termed induction.

    An inducer is the agent that

    persuades cells to be induced.

    Furthermore, each compartment of

    cells must be competent to respondto the induction process.

    There is evidence that over time,populations of embryonic cells vary

    their competence from no response

    to maximum response and then back

    to no response. In other word, there

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    is a window of competence of

    varying duration for different

    population of cells.FORMATION OF THE 3-

    LAYERED EMBRYO (i.e. the

    differentiation of the Primary Germ

    Layers)After fertilization, the mammalian

    development involves a phase of

    rapid proliferation and migration of

    cells with little or no differentiation.

    The proliferative phase lasts until 3germ layers are formed.

    1st Phase of Development

    After fertilization, the fertilized

    ovum travels through the oviduct

    and reaches the uterus. During thispassage, the cells undergo rapid

    mitosis so that it forms a solid mass

    of 16 cells, which at this stage is

    called Morula.

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    With the ovum in the uterine cavity,

    fluid enters the morula and

    accumulates in an eccentric location.The fluid-containing cavity is now

    called Blastocoele and the embryo at

    this stage is called Blastocyst.

    Within the blastocyst, 2-cellpopulation can now be

    distinguished. (1) Those lining the

    cavity (Primary Yolk-sac) are called

    Trophoblast cells and a small cluster

    of cells within the cavity called innercell mass or Embryo blast.

    The embryo blast cells form the

    embryo proper whereas the

    trophoblast cells are associated with

    the implantation of the embryo andthe formation of the placenta.

    As soon as the Blastocyst is

    implanted into the Uterine

    Endometrium, the embryo blast

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    FORMATION OF THE NEURAL

    CREST AND THE FATE OF

    THE GERM LAYERS

    It has been established that the

    formation of the 3-layered embryo

    occurs during the 3-4 weeks of

    development. These initial events

    involve cell proliferation andmigration.

    In the next 3-4 weeks of

    development, major tissues and

    organs differentiate from the 3-

    layered (Triploblastic) embryo. Thehead, face and tissues contributing to

    the development of the teeth also

    differentiate during this period.

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    The major key events that occur

    during this period involve: (a) the

    differentiation of the nervous systemand neural crest tissue from the

    Ectoderm, (b) the differentiation of

    mesoderm and (c) the folding of the

    embryo in 2-planes along the cauda-cephalic (tail-head) axis and lateral

    axis.

    The nervous system develops as a

    thickening within the ectodermal

    layer at the head - end of theembryo. This thickening constitutes

    the neural plate, which rapidly form

    raised margins, i.e. the neural folds.

    These folds in turn encompass and

    delineate an increased midlinedepression i.e. the neural groove.

    The folds eventually fuse so that a

    neural tube now separates from the

    ectoderm forming the floor of the

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    amniotic cavity with mesoderm

    intervening. From the neural tube,

    the brain and the spinal corddevelop. In the mammalian embryo,

    a group of cells separates from the

    lateral aspect of the neural plate and

    not from the crest but thename/term, neural crest cells, has

    been entrenched and retained for

    these groups of cells.

    These groups of cells (neural crest

    cells) have the capacity todifferentiate extensively within the

    developing embryo giving rise to a

    number of structure, e.g. the sensory

    ganglia, sympathetic neurons,

    Schwann cells, pigment cells,meninges and the cartilage of the

    branchial arches. They also form

    most of the embryonic connective

    tissue in the facial region. The

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    contribution of the neural crest cells

    is so extensive and their contribution

    so significant that they have beenconsidered as a fourth (4th) germ

    layer.

    In a dental context, the proper

    migration of neural crest cells isessential for the development of the

    face and the teeth. In Treacher

    Collins Syndrome (mandibulofacial

    dysostosis) full facial development

    is prevented by interference in themigration of neural crest cells to the

    facial region. All the tissues of the

    teeth, except enamel, and its

    supporting apparatus are derived

    directly from neural crest; theirdepletion will prevent proper dental

    development.

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    Derivatives from the Mesoderm

    Paraxial Mesoderm: This forms

    segmental blocks somites and eachsomite contributes to 2 adjacent

    vertebrae and their disks, a

    segmental mass of muscles and the

    dermis of the associated skin.Intermediate Mesoderm: It gives rise

    to the urogenital system.

    Lateral Plate Mesoderm: forms the

    connective tissue of the muscles

    and viscera, the serous membraneof the pleura, pericardium and

    peritoneum, blood and lymph

    cells; and the cardiovascular and

    lymphatic system as well as

    spleen and adrenal cortex.As a result of lateral folding, the

    ectoderm of the floor of the amniotic

    cavity now encapsulates the embryo

    and forms the surface epithelium.

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    The paraxial mesoderm remains

    adjacent to the neural tube and

    notochord.The lateral plate mesoderm cavitates

    to form a space (coelom) and the

    mesoderm bounding this cavity now

    lines the body wall and gut. Theintermediate mesoderm becomes

    relocated to a position on the dorsal

    wall of the coelom. The Endoderm

    forms the gut.

    One of the derivatives of mesodermis mesenchyme i.e. the embryonic

    connective tissue.

    The neural crest cells also give rise

    to mesenchyme, which is termed

    ectomesenchyme to distinguish itfrom other mesodermal

    mesenchyme.

    In summary, early stages of

    embryonic development involve

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    rapid cell proliferation and some

    histodifferentiation leading quickly

    to the formation of a trilaminar diskconsisting of 3 layers which are the

    ectoderm, mesoderm and endoderm

    with a head to tail axis fold

    established. The nervous systemdevelops from the ectoderm of this

    disk through the development of

    folds. These folds also spin off

    neural crest cells that contribute

    extensively to many tissues of theembryo including most of the dental

    tissues. All the tissues of the embryo

    arise from these 4-cell populations.

    The shape of the embryo is

    determined by the folding of the diskin 2 planes along the caudacephalic

    and lateral axes with the head fold

    being crucial to the establishment of

    the primitive mouth.

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    Environmental factors have

    relatively little impact on the

    production of congenital defectsduring the early stages of

    development because their effects

    are masked. If damage is slight,

    proliferative activity is so great thatthe damage can easily be

    compensated for by the replacement

    of new cells. If the damage is severe,

    the embryo dies. Environmental

    effects are however significant in thelater stages of embryonic

    development.

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