Chapter 3 biology Flashcards

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1
Q

VIP NOTES:

A

A secondary oocyte is ovulated from the follicle on approximately day 14 of the menstrual cycle.

The secondary oocyte travels into the fallopian tube, where it can be fertilized up to 24 hours after ovulation.

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2
Q

Where does fertilization occurs ?

A

It occurs in the widest part of the fallopian tube, called the ampulla.

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3
Q

Explain the full pathway of fertilization (9 BIGS STEPS)?

A

1) SPERM TRAVEL: Sperm swim to the fallopian tube, specifically the ampulla.
2) CAPACITATION OF THE SPERM: The head of the sperm has different types of proteins (like glycoproteins) molecules and cholesterol. So, capacitation is basically “ the cleaning off the head of the sperm, so after the capacitation it will only have modified glycoproteins left over” + “ increases the motility of the sperm=being hypermotile”
3) MOVING THROUGH THE CORONA RADIATA: When it reaches the egg, it has to push through the corona radiata, which contain the granulosa cells that produces hyaluronic acid. Because of the sperm is now hypermotile it will help the sperm to move through the corona radiata. (NOTE: Sperm move faster in alkaline environments than in acidic environements, accordingly the hypermotility will try to resist that hyaluronic acid environment.)
4) SPERM BINDING: Now that the zona plucida is available to the sperm, it then binds onto the sperm receptors (zona pallucida type 3 protein; ZP3 receptors) on the zona pellucida, recognized by specific proteins on the sperm that can recongize these ZP3 receptors.
5) ACROSOMAL REACTION: once a sperm attach to the sperm recetors on the zona pellucida it intiate the Acrosomal Reaction, where calcium ions start getting the sperm cells and causes the sperm to fuses its acrosome vesicles and releases acrosomal enzymes/digestive enzymes/ hydrolytic enzymes (acrasin and proteases) that helps to break/digest away the glycoprotein in the membrane of the zona pellucida and, thus, allow the sperm to get deeper and expose the egg’s cell membrane to the sperm. NOTE: THE FIRST EGG TO MAKE CONTACT WITH THE EGG’S CELL MEMBRANE WILL BE THE ‘WINNER’ AND FERTILIZE THE EGG.
6) FAST BLOCK TO POLYSPERMY: The egg’s cell membrane also has specific proteins where the sperm can bind to it. The sperm also have 2 types of proteins (beta and alpha) that will bind to the proteins on the egg’s cell membrane. Once the beta protein interacts with the proteins on the egg’s cell membrane, it opens specific sodium ion channels on the membrane and allow sodium ions to follow into the egg= deplorization of the egg. This deplorization inhibits the following sperms (like the ones still in the acrosomal reaction) from binding onto the egg’s cell membrane.
7) FORMATION OF ACROSOMAL APPARATUS + TRANSFER OF GENETIC MATERIAL: Alpha protein binds to the proteins on the egg’s cell membrane and allows the sperm’s and egg’s cell membrane to fuse. The first sperm to come into direct contact/touch with the egg’s cell membrane forms a tube-like structure known as the acrosomal apparatus, which helps to penetrate the cell membrane and allow the cell membrane of the sperm to fuse with cell membrane of the egg and, thus, transfer the pronucleus (sperm’s nuclear material) into egg once meosis II is complete.
—— The now depolarized and impenetrable membrane is called the fertilization membrane
8) CORTICAL REACTION (ONE MORE BLOCK TO PLOLYSPERM): once penetration of the sperm through the egg’s cell membrane and transfer of genetic material is complete, it causes the Smooth ER in the egg to be activated and start releasing calcium ions. The increased concentration of calcium ions in the egg’s cytoplasm causes the cortical granule (lysosomes) to be released into the zona pellucida (by exocytosis through the cell membrane) and releases its hydrolytic enzymes, which also help to digest the glycoprotein and the sperm receptors (ZP3) + hardens the cell membrane = it sets a slow block of polyspermy so no other following/incoming sperms can bind and once they hit the zona pellucida, they just bounce off.
9) FORMATION OF ZYGOTE: The increased calcium concentration also increases the metabolic rate of the newly formed diploid zgyote ( IE: it tells the egg that in metaphase 2 to finish meiosis and, thus produce two habloid ovum cells: definitive and polar body; the definitive then fuses with the male pronucleus cell and form a zygote.)

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4
Q

Explain how does dizygotic (fraternal) twins occur? What happens if the zgyotes implant close together?

A

It forms from fertilization of two different eggs, released during one ovulatory cycle, by two different sperms. Each zgyote will then implant into the uterine wall and each develops its own placenta, chorion, and amnion.

If the zgyotes implant close together, the placentas may grow onto each other.

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5
Q

Explain how does monozygotic (identical) twins occur? What happens if the division is incomplete?

A

it forms when a single zygote splits into two, where because the genetic material is identical the genomes of the offspring will be too.

If the division is incomplete, conjoined twins may results, where the two offsprings are physically attached.

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6
Q

Monozygotic twins can be classified by the number of structures they shared. Explain the 3 different types monzygotic twins can occur?

A

monochorionic/monoamniotic: twins share the same amnion and chorion.
Monochorionic/diamniotic: each have their own amnion, but share the same chorion.
dichorionic/diamniotic: each have their own amnions and chorions.

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7
Q

VIP NOTES:

A

Which type of twinnig occurs is a result of when the separation occured.

As more gestational structrues are shared, there are more risks as the fetuses grow and develop.

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8
Q

What happens at day 14 or 15 of the women’s ovulation cycle? (IE: how the egg becomes prepared for fertilization?)

A

During the 14 or 15 day of ovulation cycle, women start releasing a specific hormone called Luteinizing hormone (LH). This hornomes is released in the following pathway:
1. Hypothalamus release GnRH
2. GnRH triggers the anterior pituatory gland to release the LH. The anterior pituatory gland is also triggered by the increased concentration of the estrogen (positive feedback loop).
3. The LH hornomen then travels through the bloodstream and goes down to the ovaries. The LH hormone then tells the ovaries to produce lots of fluid to pressurize the graafian follicle (containing the secondary oocytes/egg) + other steps, which at the end helps to pop out the secondary oocyte and the fimbrae helps to move the secondary ooocyte to the ampulla. There fertilization takes place. NOTE: this secondary oocyte means that it underwent through miosis I and it is paused at mieosis II (particularly metaphase II). The reason for that pause is particularly because that secondary oocyte is waiting for a sperm cell to touch it (sperm attaching to the zp3 receptors) and once a sperm does, the oocyte can actually finish meiosis II to get itself ready for the pronucleus of the sperm to get into it. Then it fuses with it and finally form the diploid zygote cell.

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9
Q

After fertilization in the fallopian tubes, where does the zygote go next? What happens if it travels too late?

A

The zygote must travel to the uterus for implantation.

There will no longer be an endometrium capable of supporting the embryo.

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10
Q

What happens as the zygote moves to the uterus for implanatation?

A

As the zygote moves to the uterus for implanatation, the zygote undergoes rapid mitotic cell division (cell proliferation) in a process known as cleavage.

In this process, the diploid zygote cell undergo division 1 that produces 2 cells (2-cell stage). Then division 2 to produce 4 cells (4-cell stage). Then division 3 to produce 8 cells (8-cell stage). And lastly division 4 to produce 16 cells (16-cell stage).

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11
Q

What is the product after the first cleavage process?

A

The first cleavage officially creates an embryo, which nullifies the zygote primary characteristic: being unicellular.

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12
Q

Although several rounds of mitosis occur, the total size of the embryo remains unchanged during the first few divisions. BUT, by divising into progressively into smaller cells, the cells increase two ratios, what are they?

A

The nuclear-to-cytoplasm ration

                     AND

Surface area to volume ratio.

THUS, the cells achieve increased area for gas and nutrient exchange relative to overall volume.

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13
Q

What are the two types of cleavage? Explain each one.

Monozygotic twins orginate from which type of cleavage?

A

Indeterminate cleavage: results in cells that can develop into complete organisms

Determinate cleavage: results in cells with their fates, as the term implies, already determined. IE: these cells are committed to undergo the differentiation process to develop into a particular type of cell.

— Monozygotic twins orginate from the indeterminatly cleavaged cells of the same embryo.

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14
Q

What is Morula and Blastomeres?

A

A structure consisting of a hollow mass of cells. IE: it is anything from 16-cell stage until the blastocyst is called the morula.

The 16 or plus cells itself is called the blastomeres.

IE: Morula is a stage in embryonic development pathway consisting of blastomeres (16 or plus cells).

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15
Q

Once the morula is formed, it undergoes what process? Describe it.

A

Once the morula is formed, it undergoes the process of blastulation.

This process forms the blastula, which is a hollow ball of cells with a fluid-filled inner cavity known as the blastocoal.

The mammalian blastula is known as the blastocyst and consists of two noteworthy types of cell groups:
* A bunch of blastomeres cells clump together towards one edge and form the **inner cell mass–> Embryo blast ** that protrudes into the blastocoal (not all of it but only toward one edge) and give rise to the organism itself.
* The surrouding circular blastomeres cells become the **outer cell mass–> Trophoblast cells ** surrouding the blastocoal and give rise to the chorion and later to the placenta.

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16
Q

Trophoblast cells then develop into what (2 things)? Embroblast then develop into what (1 thing)?

A

Trophoblast (chorion/placenta): Cytotrophoblast (differentriate into this first) and synetrophoblast (differentiate into this second)

Embroblast (the organism itself): Bilaminar disk.

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17
Q

Once the blastula is implanted into the endometrium (uterus cavity lining), explain how does the trophoblast differentiate into the cytotrophoblast? and then the synthiotrophoblast?

A

Blastula is currently implanted into the endometrium:
1. Some of trophoblast cells (cytotrophoblast) start profilerating alot and as they profilerate these cell start moving out of the zona plucida (by releasing particular enzymes that allows it to move beyond the zona plucida) and its cell membrane to disintegrate/break into smaller pieces to the point of an area (like fingers) where all the cytoplasm and nuclei of these disintegrated cells are located; this area is called the synthium pool–> syntiotrophoblast.
2. This basically means that the cytotrophoblast cells is line of distinct cells and the ‘finger areas’ with floating cytoplasm and nuclei is the syntiotroblast cells, where eventually the cytotrophoblast cells will also start profilerating and enterning a villi into the syntiotrophoblast.
3. Overtime, the syntiotrophoblast will release specific hydrolytic enzymes that allow it to move deeper into the uturus cavity lining and eventually becoming confluent with maternal blood vessels. By this way, the embryo can grow by recieving oxgyenated blood, nutrients, hormones, etc from the mother via the maternal blood vessels.

WATCH NINJA NERD FOR BETTER UNDERSTANDING (4:00-7:00)

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18
Q

NOTE:

A

NO PREGNANCY: Progestrone level drops = shedding of the endometrium lining

THERE IS PREGNANCY: Cytotrophoblast release a hornome called (B-HCG), it triggers the corpus letueum to release progestrone = prevent shedding of the endometrium lining along with the implanted embryo.

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19
Q

The blastula moves from the fallopian tube to the uterus, where it burrows into the endometrium (the blastula has specific types of proteins that allows it to hook into the endometrium; IE: the uturine cavity).

What does the trophoblastic cells give rise to?

A

The trophoblastic cells give rise to the chrion, which is an extraembroynic membrane that develips into the placenta. The chrion contain chorionic villi (also formed by trophoblast), which are microscopic finger-like projections that penetrate the endometrium and as the placenta forms, it help to support the maternal-fetal gas exchange.

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20
Q

What is the umbilical cord?

A

The embryo is connected to the placenta by the umbilical cord, which consists of two arteries and one vein encased in a gelatinous substance.

The vein carries freshly oxgyenated blood rich with nutrients from the placenta to the embryo.
The arteries carry deoxgyenated blood and waste from the embryo to the placenta.

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21
Q

In addition to the placenta, what else does the chorion form?

A

it also forms an outer membrane around the amnion for additional layer of protection.

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22
Q

What is yolk sac, allantois and amnion? Also mention what is umbilical cord formed from?

A

Until the placenta is functional, the embryo is supported by the yolk sac which is also the site of early blood cell development.

The allantois is involved in early fluid exchange between the embryo and the yolk sac. Later, the umbilical cord is formed the remnants of yolk sac and the allantois.

The allantois is surrounded by the amnion, which is thin and tough membrane filled with amnotic fluid which serve as a shock absorbed during pregnancy, as it helps in lessening the impact of maternal motion on the developing embryo.

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23
Q

GASTRULATION: What is the process that occurs after implantation (what happens after the formation of the blastocyst)?

A

Once the cell mass (blastocyst) is formed and implanted into the endometrium at the uterus undergo another developmental process known as the gastrulation process, which is the development of three distinct cell layers.

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24
Q

What does the blastopore develops into for deuterostomes? For Protostomes?

A

Deuterostomes: anus
Protostomes: mouth

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25
Q

What happens during the gastrulation process? What is the end result/product of the gastrulation process called? (mention archenteron and blastophore)

A

End product is called a gastrula and it forms in the following way:
1. First the bilaminar disk is composed of two layers: epiblast(top) and hypoblast(bottom); two cavities: Amnion (top of epiblast) and yolk sac (below hypoblast).
2. START: epiblast cells signal each other to form a thick area
3. Cells at this area then starts dying and forming a clear invagination area into the blastcoal and other cells continue moving towards the invagination, called the archenteron (later develop into the gut/gastrointestinal tract). The opening of the archenteron is called the blastopore.

26
Q

Explain how are the three germ cell layers formed?

A

After the formation of archenteron, some cells will migrate into the remains of blastocoal. This occurs in the folllowing way:
1. Epiblast cells lining the archenteron invagination release chemicals and then the chemicals go close to the surrounding epiblast cells and cause them to migrate loosely (IE: not connected to each other anymore because the protein between them is broken).
2. These migrating cells are now stimulated to move towards the remaining blastocoal/archenteron.
3. Now the hypoblast cells are replaced by the migrating epiblast cells and called the endoderm (some books state that this layer still have some hypoblast cells). Other subsequent migrating epiblast continue moving and form the mesoderm. And the original epiblast layer is now called the ectoderm.

27
Q

What does each germ layer develop into?

A

Ectoderm: integument- epidermis, hair, nails, epithelia of (nose, mouth, and lower anal canal), lens of the eyes, nervous system, and inner ear.

Mesoderm: Several systems- musculoskeletal, circulatory, and most of the excretory systems + also give rise to the gonads and the musclular and connective tissue layers of the digestive and respiratory systems and the adrenal cortex.

Endoderm: epithelial lining of the digestive and respiratory tracts + following organs derived from the endoderm- pancreas, thyroid, bladder, distal urinary tracts, and parts of the liver.

28
Q

What is the adrenal cortex derived from? adrenal medulla?

A

Adrenal cortex: mesoderm
Adrenal medulla: ectoderm

29
Q

How is it that cells with the same genes are able to develop into such distinctly different cell types with highly specialized functions?

A

It is primarly due to the selective transcription of the genome. This basically means only the genes needed for that particular cell type are transcriped.

FOR EXAMPLE: in pancreatic islet cells thee genes to produce specific needed hormones (insulin, glucagon, or somatostatin) are turned on, while these same genes are turned off in other cell types because it is not needed (other genes needed for other cell types are turned on).

30
Q

What is meant by the concept of induction? what chemical substances is used in that process? and what two type of cells release-respond to these substances?

A

Selective transcription is often related to the concept of induction, which is the ability of one group of cells to influence the fate of nearby cells.

This process is mediated by chemical substances called inducers which diffuse from the organizing cells to the responsive cells.

NOTE: induction also ensures the proximity of different cell types that work together within in an organ

31
Q

Once the three germ layers are formed, what process takes place?

A

Neurulation process, which is the development of the nervous system

32
Q

Explain the full process of neurulation?

A
  1. A rod of mesodermal cells known as the notochord forms along the long axis of the organism like a primitive spine.
  2. The notochord induces a group of overlying ectodermal cells to slide inward to form the neural folds, which surround the neural groove.
  3. The neural golds grow towards one another until they fuse into a neural tube, which give rise to the central nervous system.
  4. At the tip of each neural fold are neural crest cells, which migrate outward to form the peripheral nervous system (including the sensory ganglia, autonomic ganglia, adrenal medulla, and schwann cells) as well as specific cell types in other tissues (such as the calcitonnin-producing cells of the thyroid, melanocytes in the skin, and others).
  5. Finally, the ectodermal cells migrate over the nueral tube and crest to cover the rudimentary nervous system.
33
Q

What are teratogens?

A

Early development is a highly sensitive time. During this stage, substances (known as teratogens) can interfere with development, causing defects or even death of the developing embryo.

34
Q

VIP NOTES:

A

Each teratogen will not have the same effect on every embryo. It is believed that the unique genetics of the embryo influences the effects of the teratogen.

35
Q

In addition to genetics, what are the other 5 ways that affect the outcome of teratogen?

A

In addition to genetics:
* route of exposure
* length of exposure
* rate of placental transmission of the teratogen
* exact identity of the teratogen
will also affect the outcome.

36
Q

What are common examples of teratogens?

A

Alcohol
prescription drugs
viruses
Bacteria
Environmental chemicals include polycyclic aromatic hydrocarbons.

37
Q

In addition to teratogens, maternal health can also influence development. Certain conditions may cause changes in the overall physiology of the person who is pregnant resulting in overexposure or underexposure of the embryo or fetus to certain chemicals. What are the two examples related to diabetes + hyperglacemia and maternal folic acid deficiency?

A

Diabetes + Hyperglycemia: overexposure to sugar in utero can lead to a fetus that is too large to be delivered and that could become hypoglycemic soon after birth due to synthezing high levels of insulin to compensate.

**Maternal folic acid deficiency: ** folic acid deficiency may prevent complete closure of the neural tube, resulting in spina bifida, in which part of the nervous system are exposed to the outside world or covered with a thin membrane in which the brain fails to develop.

38
Q

^^VIP NOTES^^:

A
  • An adult human being is composed of approx. 37 trillion cells.
  • These cells are organized into tissues that form organs within organ systems
  • In order to create an organism as complex as a human being, each cell must perform a specialized function
  • In addition, the cells in an organ must be organized such that the organ can function properly. For example, pancrease must create both digestive and endocrine enzymes. The cells that synthesize the digestive enzymes must be located where cell products can enter ducts to ultimately empty into the duodenum. Likewise, the cells that synthesize endocrine hormones must be located near a blood vessel to put their products into systemic circulation.
39
Q

In order to accomplish, what three stages must the cell go through (IE: what are the 3 states of cell specialization)?

A

Specification
Determination
Differentiation

40
Q

What is the difference between specification and determination?

A

The initial stage of cell specialization is specification, in which the cell is reversibily designated as a specific cell type.

On contrast, determination is the irreversible commitment of the cell to a particular cell type/lineage (plus function) in the future.

NOTE: prior to determination the cell can become any cell type, even if it has already gone through specification. But after determination, the cell is irreverisbly commited to a specific cell lineage.

41
Q

What are the two ways by which determination may occur?

A

1) During cleavage, where the existing mRNA and protein in the parent cell has been asymmetrically distributed between the daughter cells, the presence of specific mRNA and protein molecules may result in determination.

2) Determination may also occur due to secretion of specific molecules from nearby cells. The molecules are called morphogens and may cause the neighboring cells (the cell undergoing determination) to follow a particular developmental pathway.

42
Q

VIP NOTE:

A

Determination is a commitment to a particular cell type, but note that the cell has not yet actually produced what it needs to carry out the functions of that cell type- that is actually the goal of differentiation.

43
Q

What is the process of differentiation? This process includes what changes? This process occurs due to what main reason?

A

After the fate of the cell has been determined, the cell must begin to undertake changes that cause the cell to developed into the determined/wanted cell type.

This includes changes to the structure, function, and biochemistry of the cell to match the wanted cell type. This is process is called differentiation.

Due to selective transcription

44
Q

VIP REMEMBER:

A

When cell is determined, it is committed to a particular cell lineage. When the cell differentiates, it assumes the structure, function, and biochemistry of that cell type.

45
Q

What are stem cells? Where can these cells exist?

A

Cells that have not yet differentiated or that give rise to other cells that will be differentiated.

Stem cells can exist in embryonic tissues as well as in adult tissues.

46
Q

The tissues of a particular stem cell can differentiate into are detemined by what?

A

By its potency.

47
Q

What are the three types of cell potency that stem cells can differentiate into?

A

Totipotent: It is the greatest potency and include embroynic stem cells. These totipotent stem cells can differentiate into any cell type either in the fetus (3 germ layers) or in the placental structures.

Pluripotent: after the 16-cell stage, the totipotent cells start to differentiate into the three germ cell layers. At this stage, the cells are said to be pluripotent which means that the cells can differentiate into any cell type (any germ layer and its derivates) except those found in the placental structures.

Multipotent: Stem cells that can differentiate into multiple cell types within a particular group. Like for example, hemtopoietic stem cells are capable of differentiating into all of the cells found in blood (white, red, platelets; but not skin, neurons, or muscle).

48
Q

VIP NOTES:

A

The determination and differentiation of a cell depends on the location of the developing cell as well as the identity of the surrounding cells.

The developing cell recieves signals from organizing cells around it and may also secrete its own signaling molecules.

49
Q

What is meaning of inducers? Responder? Competent?

A

As discussed previously, surrounding tissues induce a developing cell to become a particular cell type via inducers; the term inducer may also refer to the cell secreting the signal.

The cell that is induced is called a responder (responsive cell)

To be induced, a responder must be competent; meaning be able to respond to the inducing signal.

50
Q

What are the 4 signals that cell-cell communication can occur? Explain each one?

A
  1. Autocrine: signals that can act on the same cell that secreted the signal in the first place
  2. Paracrine: signals that act on cells in the local area
  3. Juxtacrine: signals that do not usually involve diffusion, but involve a cell directly stimulating receptors of an adjacent cell.
  4. Endocrine: signals that involve secreting hormones that travel through the bloodstream to a distant target tissue.
51
Q

Inducers are usually what?

A

Inducers are usually growth factors, which are peptides that promote differentiation and mitosis in certain tissues.

52
Q

VIP NOTE:

A

Most growth factors (inducers) only function on specific cell types or in certain areas, as determined by the competence of these cells.

For example, PAX6 is expressed in the ectoderm of the head, but in no other location. Therefore, as the optic vesicle approaches the overlying ectoderm producing this factor, development of the lens of the eye is induced.

53
Q

Interestingly, induction is not always a one-way pathway for the course of development. What is the meaning of reciprocal induction?

A

If two tissues both induce further differentiation in each other, this is called reciprocal induction.

For example, differentiation of the lens then trigger the optic vesicle to form the optic cup, which ultimately becomes the retina. IE: most tissues will be exposed to multiple inducers during the course of development.

54
Q

What is one of the main methods of signaling? A common example?

A

Via the use of gradients. A common example of that is morphogens which diffuse throughout the organism.

Common example of morphogens are TGF-B, Shh, and EGF.

55
Q

VIP NOTES:

A
  • Induction and differentiation lead to the creation of different types of cells; however, these cells are not always in the right location to carry out their function.
  • Further, the sculpting of various anatomic structures requires not only differentiation, but also the death of some cells.
  • Certain organs also have the ability to recreate injured or surgically removed portions of tissue.
56
Q

What is cell migration? Give two well known example mentioned in the book?

A

Cells (differentiated cells) must be able to disconnect from adjacent structures and migrate to their correct location in order carry out their function.

  1. Anterior pituatary gland originates from a segment of oral ectodem and must migrate from the top of the mouth to its final location just below the hypothalamus
  2. Neural crest cells also undergo extensive migration: these cells form at the edge of the neural folds during neurulation and then migrate throughout the body to form many different structures including the following: sensory ganglia, autonomic ganglia, adrenal medulla, schwann cells, and as well as specific cell types in other tissues such as calcitonin-producing cells of the thyroid and melanocytes in the skin.
57
Q

What is apoptosis? How can it occur?

A

Programmed cell death that occurs at varrious times during development.

Apoptosis allows for the recycling of materials.

It can occur via apoptotic signals or pre-programming.

58
Q

Explain what happens during the apoptosis process? (make sure to explain what is apoptotic blebs and apoptotic bodies?u

A

During the process of apoptosis:
1. The nucleus condenses (pyknosis: irreverisble condensation of the chromatin during the process of apoptosis).
2. Cell shrinkage
2. the cell undergo changes in morphology and divides into many self-containing protrusions called apoptotis blebs
3. The apoptotic blebs can then be broken apark into apoptotic bodies and then can be digested by other cells (phagocytes engulfs the apoptotic bodies).

59
Q

What is the benefit of the formation of apoptotic blebs?

A

Because the blebs are contained by a membrane, this prevents the release of potentially harmful substances into the extracellular membrane.

60
Q

What is necrosis?

A

A process of cell death in which a cell dies as a result of injury and the internal substances can be leaked, causing irritation of nearby tissues or even an immune response.

61
Q

List the differences between apoptosis and necrosis? (SOURCE: GOOGLE- WIKIPEDIA IMAGRES)

A

Apoptosis:
* The nucleus begins to break apart
* Chromatin condenses and breaks into smaller pieces
* The organelles are located in the belbs.
* LOOK AT THE WIKIPEDIA IMAGE

Necrosis:
* The structure of the nucleus changes
* The belbs fuse with each other and become bigger
* no organelles located in the belbs
* LOOK AT THE WIKIPEDIA IMAGE