DA2 Flashcards

1
Q

Fate of embryonic epiblast cells

A
  • Those on midline form the primitive streak
  • Some displace hypolast to form endoderm
  • Some migrate between epiblast and endoderm to form mesoderm
  • The rest become ectoderm
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2
Q

Roles of primitive streak

A
  • Establishes the longitudinal (cranial-caudal) axis of embryo
  • Is the master organizer of mesoderm as segregation of epiblast cells occus according to area of streak they migrate
    • Through primitive node - form notochord
    • Caudal to node - form paraxial mesoderm
    • Through midstreak - form intermediate mesoderm
    • Caudal to streak - form lateral plate mesoderm
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3
Q

Neurulation

A

Establishment of nervous system

  • Notochord induces formation of neural plate
  • Folds of neural plate fuse to establish neural tube
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4
Q

Roles of notochord

A
  • Inductor of CNS
  • Supporting structure for developing embryo
  • Formation of vertebral column (persists in adults as nucleus pulposus)
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5
Q

Neurulation: Neuropores

A
  • Temporary communication of neural tube with amnion
  • Neural tube differentiates to form brain vesicles, spinal cord
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6
Q

Neurulation - Neural Crest Cells

A

Break free from the crest of neural plate

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7
Q

Derivatives of pluripotent crest cells

A
  • Sensory and autonomic ganglia
  • Adrenal medulla
  • Melanocytes
  • Connective tissue structures of the head and face
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8
Q

Paraxial Mesoderm

A
  • Becomes segmented into paired somites
  • Formed successivley, unidirectionally
  • Number of pairs is species-specific
  • Used to estimate age of embryo
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9
Q

Somites

A

the foundation of metameric organization of body

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10
Q

Intermediate mesoderm differentiates into_______.

A

Urogenital structures

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11
Q

Lateral plate mesoderm divides into two layers:

A
  1. Dorsal layer associates with ectoderm to form parietal pleurae/peritoneum
  2. Ventral layer associates with endodern to form visceral pleurae/peritoneum
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12
Q

Space between the dorsal layer and ventral layer of the divded lateral plate mesoderm

A

Intraembryonic body cavity (coelom)

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13
Q

Establishment of cylindrical body form

A

Initiated by differential growth and body foldings

  • Head fold: brain extends into amniotic cavity and folds ventrally
  • Tail fold: proceeds cranially
  • Lateral folding: proceeds bidirectionally
  • Result: incorporation of coelom and yolk sac into the body
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14
Q

Body form result:

A

Tube-within-a-tube cylindircal body

  • Outer tube represents the body wall
  • Inner tube represents the primitive gut
  • Space between the two represents the body cavity
  • Middle part of the tube remains temporarily
  • In fetal stage olk sac is replaced by umbilical cord
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15
Q
A
  • A - communication of intraembryonic and extraembryonic cavities
  • B - narrowing of the wide connection between the two cavities
  • C - completion of cylindrical body
  • Figure C:
    • 1 - Body cavity
    • 2 - Primitive gut
    • 3 - Body wall
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16
Q

Placodes

A

Ectodermal thickenings in head region; form sensory organs

17
Q

Pharyngeal arches

A

agregations of mesoderm in head region

18
Q

Basic Processes of Development: Growth

A
  • Most outstanding event in early development
  • Differential growth - accounts for diversity of form
  • Growth rate of different parts are relatviely constant within same species
  • Growth is controlled and made possible by a number of factors (constitutional, nutritional, hormones, vitamins, growth-arresting)
19
Q

Basic Processes of Development: Differentiation

A

Development of specialized cell types

  • Is antagnoistic to growth
  • Is determined by cell’s genome and its position in embryo
  • Is determined by interactions and effective communication between cells
  • Induction: a group of cells directs differentiation of other cells (essential part of cell differentiation)
20
Q

Stages in cell differntiation

A
  • Uncommited (totipotent) cell: to 8-cell morula stage
  • Commited (pluripotent): cell with restricted developmental potential
21
Q

Phases of commitment

A
  • Specification: cell can differentiate autonomously
    • Transitional commitment –> reversible commitment (cloning)
    • A cell can be re-programmed to give rise to any cell type
  • Determination: stage of irreversible commitment
    • Conditional commitment –> regulative development
    • The halved number of cells alter their fat to produce a complete organisms
    • Critical in development of identical twins
22
Q

Basic Processes of development: Morphogenesis

A
  • A mass of cells becomes a structure morphogenic field - a subset of cells forming an organ (each field - controlled by tissue-master genes)
23
Q

Basic Morphogenic Processes

A
  1. Cell migration: controlled and influenced by interaction with their environment
  2. Cell aggregation: cells with like tissue-receptors adhere to form compact masses
  3. Splitting - cells delaminate and reaggregate to form new layers
  4. Fusion - growth together of two localized areas
  5. Cell Death - apoptosis, essential for shaping complex organs
  6. Folding - outward (evagination, outpocketing); inward (invagination, inpocketing); linear (groove)