Chapter 3 Embryogenesis And Develoment Flashcards

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1
Q

Fertilization

A

Usually occurs in the widest part of the fallopian tube (the AMPULLA). When sperm meets the secondary oocytes, It releases acromial enzymes that allow the head of the sperm to penetrate the Corona radiata and zona pellucida.

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2
Q

Acrosome

A

Sperm organelle that covers the sperm nuclei and contains acrosomal enzymes that help penetrate the egg. After the first sperm comes in contact with the secondary oocyte, it forms a tube like structure known as the acrosomal apparatus.

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3
Q

Cortical reaction

A

Release of calcium ions after penetration of the sperm through the cell membrane. These calcium ions depolarize the membrane of the ovum which prevents fertilization of the ovum by multiple sperm cells, and increases the metabolic rate of the newly formed diploid zygote.

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4
Q

Fertilization membrane

A

Depolarized impenetrable membrane that form as a result of the cortical reaction, prevent fertilization of the ovum by multiple sperm cells.

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5
Q

Two different mechanisms of twinning.

A

Dizygotic (fraternal) twins

Monozygotic (identical) twins

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6
Q

Dizygotic (fraternal) twins

A

Forms from the fertilization of two different eggs released during one ovulatory cycle by two different sperm. No more genetically similar than any other pair of siblings.

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7
Q

Monozygotic (identical) twins

A

Form when a single zygote splits into two. Because the genetic material is identical, the genome of the offspring will be too. If division is incomplete, conjoined twins may result where the two offspring are physically attached.

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8
Q

Three types of monozygotic twins

A

Monochorionic/monoamniotic: share the same amnion and chorion

Monochorionic/diamniotic: have their own amnion, but share the same chorion

Dichorionic/diamniotic: each have their own amnions and chorions

The type of twinning that occurs is a result of when the separation of the zygote occurred.

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9
Q

Embryonic ceavage

A

Rapid mitotic cell division as the zygote moves to the uterus for implantation. The first cleavage officially creates an embryo, as it nullifies one of the zygotes defining characteristics: unicellularity. The process of rapid cell division that occurs in an embryo after fertilization.

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10
Q

Two types of cleavage, explain.

A

Indeterminate cleavage (produces cells that have potential to develop into a complete organism) and determinate cleavage (cells have a predetermined developmental fate).

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11
Q

Indeterminate cleavage

A

Results in cells that can still develop into a complete organism.

Fun fact, monozygotic twins have a identical genome because they both originate from indeterminately cleaved cells of the same embryo.

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12
Q

Determinate cleavage

A

Results in cells with fates that are already DETERMINED, as the name implies. In other words, these cells are committed to differentiating into a certain type of cell.

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13
Q

Morula

A

Solid ball of cells, several divisions after fertilization. Comes from the Latin word for mulberry, which might help us grasp what an embryo at the stage looks like.

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14
Q

Blastula

A

Once the morula is formed, it undergoes blastulation which forms a blastula: hollow ball of cells with the fluid filled inner cavity known as a blastocoel. The mammalian blastula is known as a blastocyst.

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15
Q

Blastocyst

A

The mammalian blastocoel is known as a blastocyst, consisting of two noteworthy cell groups: the trophoblast and the inner cell mass.

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16
Q

Trophoblast cells

A

Surround the blastocoel and give rise to the chorion and later the placenta.

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17
Q

Inner cell mass

A

Protrudes into the blastocoel and gives rise to the organism itself.

The trophoblast gives rise to the placenta. The inner cell mass gives rise to the organism.

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18
Q

Chorion

A

Trophoblastic cells give rise to the chorion, an extraembryonic membrane that develops into the placenta.

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19
Q

Chorionic villi

A

The trophoblasts form the chorionic villi, which are microscopic fingerlike projections that penetrate the endometrium and develop into the placenta that support maternal-fetal gas exchange.

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20
Q

Umbilical cord

A

Connection between the embryo and the placenta. Consists of two arteries and one vein encased in a gelatinous substance. The vein carries freshly oxygenated blood rich with nutrients from the placenta to the embryo, the umbilical arteries carry de oxygenated blood, and waste to the placenta for exchange.

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21
Q

Anatomy of pregnancy

A
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22
Q

Ectopic pregnancy

A

Occurs when the blastula implants itself outside the uterus. Over 95% of ectopic pregnancies occur in the fallopian tubes. Generally not viable because the fallopian tube is not an environment in which an embryo can properly grow. A suspected ectopic pregnancy is often a surgical emergency.

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23
Q

Yolk sac

A

Site of early blood cell development, support the embryo until the placenta is functional.

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24
Q

Two noteworthy extra embryonic membranes

A

Allantois (Alan-tow-iss) and amnion.

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25
Q

Allantois

A

Involved in early fluid and gas exchange between the embryo and the yolk sack. The UMBILICAL CORD is formed from remnants of the yolk sac and the allantois.

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26
Q

Amnion

A

Surrounds the allantois. The amnion is thin, tough membrane filled with amniotic fluid. Serves as a shock absorber during pregnancy.

The allantois is a hollow sac-like structure filled with clear fluid that forms part of a developing amniote’s conceptus (which consists of all embryonic and extraembryonic tissues). It helps the embryo exchange gases and handle liquid waste.

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27
Q

Amniocentesis

A

Process of aspirating amniotic fluid by inserting a thin needle into the amniotic sac. the amniotic fluid contains fetal cells that can be examined for chromosomal abnormalities as well as sex determination. Opportunity for early screening tests.

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28
Q

Gastrulation

A

The generation of three distinct cell layers once the cell mass implants known as the primary germ layers: endoderm, mesoderm, ectoderm.

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29
Q

Early stages of embryonic development (from fertilization to babies)

A

Zygote, morula, blastocyst, gastrula (with archenteron and blastopore), embryo, fetus, babies.

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30
Q

Gastrula

A

Invaginated blastula

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31
Q

Archenteron

A

Name for the invaginated membrane into the blastocoel, later develops into the gut.

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32
Q

Blastopore

A

The opening of the archenteron.

In deuterostomes, the blastopore develops into the anus.

In protostomes, the blastopore develops into the mouth.

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33
Q

Dueterostomes and protostomes

A

Dueterostomes, such as humans, the blastopore develops into the anus.

In protostomes, such as anthropods and mollusks, the blastopore develops into the mouth.

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34
Q

Primary germ layers

A

Ectoderm, mesoderm, endoderm

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35
Q

Ectoderm

A

Outermost layer of the three primary germ layers. Gives rise to the integument (skin), including the epidermis, hair, nails, and the epithelia of the nose, mouth, and lower anal canal. Also gives rise to the lens of the eye, THE NERVOUS SYSTEM, and inner ear.

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36
Q

Mesoderm

A

The middle layer of the three primary germ layers. Gives rise to the muscular skeletal, circulatory system including the heart, and most of the excretory systems. Also gives rise to the gonads as well as the muscular and connective tissue layers of the digestive and respiratory systems and the adrenal cortex.

Ectoderm (outer): Skin, hair, nails, brain, spinal cord, nervous system

Mesoderm (middle): Muscles, bones, cartilage, blood vessels, kidneys

Endoderm (inner): Lining of the digestive tract, lungs, liver, pancreas

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37
Q

Endoderm

A

Innermost layer of the three primary germ layers. Forms the epithelial lining of the digestive and respiratory tract, including the lungs. The pancreas, thyroid, bladder, and distal urinary tracts, as well as parts of the liver, are derived from the endoderm.

Ectoderm (outer): Skin, hair, nails, brain, spinal cord, nervous system
Mesoderm (middle): Muscles, bones, cartilage, blood vessels, kidneys
Endoderm (inner): Lining of the digestive tract, lungs, liver, pancreas

38
Q

Tissues that arise from the three primary germ layers

A

Ectoderm (outer): Skin, hair, nails, brain, spinal cord, nervous system
Mesoderm (middle): Muscles, bones, cartilage, blood vessels, kidneys
Endoderm (inner): Lining of the digestive tract, lungs, liver, pancreas

39
Q

Dual embryonic origin of the adrenal glands.

A

The adrenal cortex is derived from the mesoderm, but the adrenal medulla is derived from the ectoderm because the adrenal medulla contains some nervous tissue.

40
Q

Selective transcription of the genome

A

Mechanism by which cells with the same genes are able to develop into distinctly different cell types with highly specialized functions. Only genes needed for that particular cell type or transcribed.

41
Q

Induction

A

The ability of one group of cells to influence the fate of nearby cells.

42
Q

Inducers

A

Cell to cell communication. Facilitates the process of induction, the process of groups of cells or tissues influencing (inducing tissue) the development of other cells or tissue (responders). Inducers diffuse from organizing cells to the responsive cells. Also ensures the proximity of different cell types that work together with an in organ. Inducer also refers to the cell secreting the signal.

43
Q

Neuralation

A

The development of the nervous system. This happens once the three germ layers are formed. The nervous system is derived from the ectoderm.

44
Q

Notochord

A

Think of the notochord as a primitive Spine. Forms from the mesoderm.

45
Q

Formation of the neural tube

A

The notochord induces a group of overlying ectodermal cells to slide inward to form neural folds, which surrounding neural groove. the neural folds grow toward one another until they fuse into a neural tube, and give rise to the central nervous system. At the tip of each general fold are neural crest cells that migrate outward to form the peripheral nervous system. Ectodermal cells will then migrate over the neural tube and crest to cover the rudimentary nervous system.

46
Q

Spinal bifida and anencephaly

A

Spina bifida is the failure of the neural tube to close which causes all or some of the spinal cord to be exposed to the outside world. Ranges from no significant distress to death.

Anencephaly Is where the brain fails to develop in the skull is left open. Universally fatal.

Folate, or folic acid, is usually prescribed to people who are likely to get pregnant to prevent this complication. Neurulation occurs before pregnancy is detected.

47
Q

Teratogens

A

Substances that interfere with development, causing defects or even death of the developing embryo. Examples include alcohol, prescription drugs, good drugs, bad drugs, drug drugs, viruses, bacteria, and environmental chemicals, including polycyclic aromatic hydrocarbons.

48
Q

Three stages of stem cell specialization

A

Specification, determination, and differentiation

Specification is reversible process where a cell commits to a cell type, but can change its fate based on different cues.

Determination is an irreversible process where a cell commits to a cell type, and its fate cannot be reversed.

Differentiation is the process where a cell develops specific characteristics, such as structure, function, and biochemistry, to become a mature cell type.

49
Q

Cell specialization: specification/determination

A

Specification is the initial stage of cell specialization, in which the cell is REVERSIBLY designated as a specific type of cell.

Determination follows specification. The commitment of a cell to a particular function in the future. Prior to determination, the cell can become any cell type, even if it has already gone through specification.
After determination, the cell is irreversibly committed to a specific lineage.

Note: determination is a commitment, but the cell has not yet actually produced what it needs to carry out the function of that type.

50
Q

Morphogen

A

Specific molecule secreted from nearby cells that caused neighboring cells to follow a particular developmental pathway. A type of determination.

Some common morphogens include: transforming growth factor beta (TGF-B), sonic hedgehog (Shh), epidermal growth factor (EGF)

51
Q

Cell specialization: differentiation. Is differentiation reversible?

A

Changing of the structure, function, and biochemistry of the cell to match the cell type. Differentiation comes after determination.

Differentiation is generally irreversible.

52
Q

Stem cells

A

Cells that have not yet differentiated or that give rise to other cells that will differentiate. Three types are embryonic stem cells, adult (somatic) stem cells, and induced pluripotent stem cells (iPSCs). Categorized by their potency: totipotent, multipotent, unipotent.

53
Q

Stem cell potency

A

Determines the tissue or particular stem cell can differentiate into.

Cells with the greatest potency are called totipotent.

Cells that can give rise to all types of all cell types in an adult organism are pluripotent.

Cells that can give rise to multiple cells within a lineage are multipotent.

54
Q

Totipotent stem cells

A

Cells with the greatest potency for differentiation, include embryonic stem cells. In differentiating to any cell type, either in the fetus or in the essential structures. After the 16 cell stage, the cells of the morula begin to differentiate into two groups: the intercell mass and the trophoblast. After a few more cycles of cell division, these totipotent cells start to differentiate into the three term cell layers

55
Q

Pluripotent stem cells

A

Can differentiate into any cell type, except for those found in the placental structures.

56
Q

Multipotent stem cells

A

Can differentiate into multiple types of cells within a particular group. For example, hematopoietic stem cells are capable of differentiating into all of the cells found in blood, including the various types of white blood cells, red blood cells, and platelets, but not into skin cells, neurons, or muscle cells. Potency is a spectrum, not a series of strict definitions.

57
Q

Embryonic stem cells image

A
58
Q

Cell to cell communication.

A

Cell to cell communication can occur via Autocrine, paracrine, juxtacrine, endocrine signals.

Note: -crine suffix means “to secrete or release”

59
Q

Responders (cell communication)

A

Responders are the cells that are being induced also referred to as the responsive cell, to be induced to responder must be COMPETENT, or able to respond to the inducing signal.

60
Q

Autocrine signals

A

Cellular communication that acts on the same cell that secreted the signal in the first place

61
Q

Paracrine signals

A

Cellular communication signals that act on cells in the local area.

62
Q

Juxtacrine signals

A

Cellular communication signals that do not usually involve diffusion, but involve a cell directly stimulating receptors of an adjacent cell. Occurs when cells are in direct contact with one another.

63
Q

Endocrine signals

A

Cellular communication signals that involve secreted hormones that travel through the bloodstream to a distant target tissue.

64
Q

Growth factors

A

Peptides that promote differentiation and mitosis in certain tissues. Most growth factors only function on specific cell types or in certain areas, as determined by the competence of these cells.

65
Q

What is reciprocal development, the embryological concept of induction?

A

Reciprocal development is an embryological concept where two tissues or structures influence each other in a two way relationship.

Example being tooth development. Dentin must develop before enamel, a process that is managed by reciprocal induction.

66
Q

Apoptosis

A

Programed cell death. The cell undergoes changes in morphology and divides into many self-contained protrusions called apoptotic blebs which can then be broken apart into apoptotic bodies.

67
Q

Cell necrosis

A

Process of cell death in which a cell dies as a result of injury.

68
Q

Regenerative capacity

A

The ability of an organism to regrow certain parts of the body.

Complete regeneration: lost or damaged tissues are replaced with identical tissues.

Incomplete regeneration implies that the newly form tissue is not identical and structure function to the tissue that has been injured or lost.

69
Q

Complete regeneration

A

Regenerative capacity in that the lost or damaged tissues are replaced with identical tissues.

70
Q

Incomplete regeneration

A

Regenerative capacity that implies that the newly form tissue is not identical and structure function to the tissue that has been injured or lost.

71
Q

Senescence

A

Biological aging. at the cellular level, senescence results in the failure of cells to divide, normally after approximately 50 divisions in vitro (in glass).

72
Q

Telomeres

A

End of chromosomes. Telomeres reduce the loss of genetic information from the end of chromosomes and help prevent the DNA from unraveling. High concentration of guanine and cytosine enable telomeres to “knot off” the end of the chromosome.

73
Q

Telomerase

A

A reverse transcriptase enzyme that is able to synthesize the end of chromosomes, and thus telomeres, prevent senescence (the process of aging). Some cells including germ cells, fetal cells, and tumor cells, expressed this enzyme.

74
Q

Placenta

A

ORGAN where nutrients, gas, and waste exchange occurs. Facilitated by diffusion, which requires a gradient, which implies there is a higher partial pressure of oxygen in maternal blood than in fetal blood.

Note: the placenta also qualifies as an endocrine organ because it produces progesterone, estrogen, and human chorionic gonadotropin (hCG), all which are essential for maintaining pregnancy.

75
Q

Fetal hemoglobin (HbF)

A

Contained in fetal blood cells and have a greater affinity for oxygen than adult hemoglobin (HbA). Further enhances the transfer of oxygen from maternal to fetal circulation.

Note: fetal blood and maternal blood do not mix. The transfer of nutrients gas and waste is facilitated via diffusion.

76
Q

Immunity regarding the placental barrier

A

The placenta barrier also serves an immunity function. The fetus is immunologically naïve because it has not yet been exposed to any pathogens. However, accidental exposure can happen in utero (in the womb).

77
Q

TORCHES mnemonic (regarding fetal pathogens)

A

TOxoplasma gondii
Rubella
Cytomegalovirus
HErpes or Hiv
Syphilis

Many pathogens are too large to cross the placental barrier by diffusion, but a set of pathogens called TORCHES infections, can cross the barrier and cause significant birth defects. Therefore, screening for (and sometimes immunization against) these infections is recommended in pregnancy.

78
Q

Arteries. Do they carry oxygenated or deoxygenated blood? Are there any exceptions to that?

A

Carry oxygenated blood away from the heart.

One artery that carries deoxygenated blood is the pulmonary artery which heads toward the pulmonary circuit.

79
Q

Veins, do they carry oxygenated or deoxygenated blood, are there exceptions?

A

Carry deoxygenated blood to the heart. Pulmonary veins carry oxygenated blood, Umbilical veins carry oxygenated blood to embryo (early stages) and fetus (9 weeks until birth).

80
Q

Umbilical arteries

A

Carry deoxygenated blood away from the fetus towards the placenta.

81
Q

Umbilical vein

A

Carries oxygenated blood toward the fetus from the placenta

82
Q

Three shunts in fetal development

A

In order from placenta to embryo and out are: ductus venosus (shunt blood away from the fetal liver) Foramen ovale, ductus arterius (shunt blood away from the fetal lungs),

These three shunts actively direct blood away from the lungs and liver because those organs are underdeveloped and sensitive to high blood pressures they will receive in postnatal life.

83
Q

Foramen ovale

A

One way valve that connects the right atrium to the left atrium in the fetus. This allows blood entering the right atrium from the inferior vena cava to flow into the left atrium instead of the right ventricle, and thereby be pumped through the aorta into systemic circulation directly.

84
Q

Ductus arteriosus

A

Shunts leftover blood from the pulmonary artery to the aorta. The pressure differential between the right and left sides of the heart pushes blood through this opening and into systemic circulation. ALLOWS BLOOD TO BYPASS PULMONARY CIRCULATION AND PROVIDE NUTRITIONAL AND OXYGEN RICK BLOOD INTO SYSTEMIC CIRCULATION.

85
Q

Ductus venosus

A

Ductus venosus is a fetal blood vessel that allows oxygenated blood to flow from the placenta to the fetal brain and heart and allows blood to bypass the fetal liver. Allows blood to go directly to the inferior vena cava from the umbilical vein.

Note: a small amount of blood makes it to the hepatic arteries in systemic circulation to allow for oxygenation and nourishment of the developing fetal liver.

86
Q

First trimester

A

The major organs begin to develop during the first few weeks. The heart begins to beat, and soon afterwards, the eyes, gonads, lens, and liver start to form. The cartilaginous skeleton begins to harden into bone. Most of the organs form. The brain is fairly developed, and the embryo becomes known as a fetus. At the end of the third month of fetus is about 9 cm long.

87
Q

Second trimester

A

The fetus undergoes a tremendous amount of growth. Its face takes on a human appearance, and its toes and fingers elongate. The fetus measures 30 to 36 cm long by the end of the sixth month.

88
Q

Third trimester

A

Characterized by continued rapid growth and further brain development. Antibodies are transported by highly selective, active transport from the pregnant individual to the fetus for protection against foreign agents and preparation for life outside the womb.

89
Q

Birth

A

The cervix thins out and the amniotic sac ruptures. Next, the strong uterine contractions result in the birth of the fetus. Finally, the placenta and umbilical cord are expelled.

90
Q

Parturition

A

Vaginal childbirth

91
Q

Two molecules that coordinate rhythmic contractions of uterine smooth muscle during childbirth.

A

Prostaglandins and the peptide hormone oxytocin.

92
Q

What do the three primary germ layers develop into humans?

A

Ectoderm: nervous system, skin, sensory organs, hair, nails, teeth enamel.

Mesoderm: muscles, connective tissues, blood and lymph vessels, heart, kidney, reproductive organs.

Endoderm: gi tract, liver, pancreas, lungs, thyroid, parathyroid glands, bladder, urethra.