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Original post by TheFootyKing19
Describe the gross structure of the human heart? (5)
Why do semi-lunar valves close?
What is the function of the valves?
What is the function of the AVN?
What is the function of the Bundle of His?
How do channel proteins work in facilitated diffusion?
Facilitated diffusuion depends on 3 factors? What are those?
Explain the process of Expiration? (5)
How is a dipeptide formed? (5)
What are the functions of proteins? (3)
Define Vaccine?
Define antibody?


It consists of the atria and ventricles. Blood flows into the right atrium from the vena cava then into the right ventricle and out through the pulmonary artery. It comes back into the left atrium through the pulmonary veins, and is pumped out by the left ventricle into the aorta.

Because the pressure in the aorta/pulmonary artery rises to above that of the ventricles.

To stop back flow of blood.

To send a wave of electrical activity down the atrioventricular septum through the bundle of His, which is released from the apex of the heart upwards from the Purkinje fibres causing ventricular systole.

To conduct the electrical impulse from AVN down to the apex of the heart and the Purkinje fibres.

Channel proteins open in the presence of particular substance which is recognised by glycoprotein or glycolipid receptors on the cell surface membrane, and allow substances to then diffuse through into or out of the cell in a controlled manner, but down the concentration gradient.

The presence of a protein carrier or channel, and concentration gradient down which substances can pass and sometimes a transmitter substance that must be present to allow the "gated" proteins to open.

Internal intercostal muscles contract bringing the ribs downwards and inwards, diaphragm relaxes into an upward dome shape. This decreases the volume of the thorax, and so pulmonary pressure is now greater than atmospheric pressure and air is forced out of the lungs. Alternatively, elastic recoil of the lungs and relaxation of the muscles may be enough to expel air.

A condensation reaction between to peptides or amino acids; a water molecule is produced as the carbon of the carboxylic acid group loses the alcohol group (OH) and the nitrogen of the amine group loses a Hydrogen. The bond is therefore formed between the carbon and nitrogen.

Proteins can form enzymes to catalyse biological reactions (globular), act as structures as fibrous proteins (muscles, tendons etc.) or as transport molecules within the cell surface membrane.

An injected substance containing dead or inactive pathogens or their antigens, which improves immunity to a disease.

A protein used to identify and neutralise foreign cells in the body.
(edited 12 years ago)
Hey me again, is the cellular response when an infected cell uses part of the antigen in a MHC 2 protein on it's cell surface membrane to activate T-killer cells

OR

When a phagocyte digests a pathogen then presents part of the pathogen on it's cell surface membrane to activate T-helper cells?

OR are they the same thing...
(edited 12 years ago)
Original post by stoppy123

Original post by stoppy123
Hey me again, is the cellular response when an infected cell uses part of the antigen in a MHC 2 protein on it's cell surface membrane to activate T-killer cells

OR

When a phagocyte digests a pathogen then presents part of the pathogen on it's cell surface membrane to activate T-helper cells?

OR are they the same thing...


Second one is correct
1) phagocyte presents antigen on its cell surface membrane
2) receptors on certain T helper cell fit exactly on to these antigens
3) this activates other t cells to divide rapidly by mitosis and form clones
4) the cloned t cells can diffrentiate into cyto toxic t cells, stimulate b cells etc


:biggrin: first one seems more complicated lol :/
Original post by maria-95
Second one is correct
1) phagocyte presents antigen on its cell surface membrane
2) receptors on certain T helper cell fit exactly on to these antigens
3) this activates other t cells to divide rapidly by mitosis and form clones
4) the cloned t cells can diffrentiate into cyto toxic t cells, stimulate b cells etc


:biggrin: first one seems more complicated lol :/


http://bcs.whfreeman.com/thelifewire/content/chp18/1802003.html

This says otherwise D:

You described the humoral response:http://bcs.whfreeman.com/thelifewire/content/chp18/1804s.swf
(edited 12 years ago)
cell mediated and humoral are very similar because they both have the activation phase. steps one two three above is where the t helper cells are activated, but then the clones that are produced will diffrentate into cyto toxic t cells ( which is explained in the link) that will kill infected cells..they do this by producing a protien which makes wholes in the membrane. so water can go in or out by osmosis and the cell will burst or shrink. ( the link has explained what the cyto toxic cells do before they have explained how they have actually come about)

Humoral immunity is when
1) the antigens of the invading pathogen are taken up by the b cell and presented on their membrane
2) t helper cells come along and bind to the processed antigens on the b cells to activate them
3) the be cells are now activated so can divide by mitosis
4) clones diffrentate into plasma cells and memmory cells and so on
Immunology will be the death of me.
Original post by maria-95
cell mediated and humoral are very similar because they both have the activation phase. steps one two three above is where the t helper cells are activated, but then the clones that are produced will diffrentate into cyto toxic t cells ( which is explained in the link) that will kill infected cells..they do this by producing a protien which makes wholes in the membrane. so water can go in or out by osmosis and the cell will burst or shrink. ( the link has explained what the cyto toxic cells do before they have explained how they have actually come about)

Humoral immunity is when
1) the antigens of the invading pathogen are taken up by the b cell and presented on their membrane
2) t helper cells come along and bind to the processed antigens on the b cells to activate them
3) the be cells are now activated so can divide by mitosis
4) clones diffrentate into plasma cells and memmory cells and so on


So.. this The cellular response is the engulfing of a antigen by a phagocyte then breaking it down and presenting it on their cell surface membrane on a receptor protein, t-helper cells bind to this protein and then are stimulated to divide into identical clones of eachother, these t-cells can then divide into memory cells, cytotoxin cells etc

The humoral response is when a b-cell comes in contact with an antigen and the b-cell breaks the antigen down partially then presents it on its plasma membrane, the t-cells then bind to this b-cell as they have come into contact with the antigen before, the b-cells are now stimulated to divide by mitosis, these clones can then become memory cells or plasma cells.
Original post by Mocking_bird
Immunology will be the death of me.


Amen to that!
Original post by stoppy123

Original post by stoppy123
So.. this The cellular response is the engulfing of a antigen by a phagocyte then breaking it down and presenting it on their cell surface membrane on a receptor protein, t-helper cells bind to this protein and then are stimulated to divide into identical clones of eachother, these t-cells can then divide into memory cells, cytotoxin cells etc

The humoral response is when a b-cell comes in contact with an antigen and the b-cell breaks the antigen down partially then presents it on its plasma membrane, the t-cells then bind to this b-cell as they have come into contact with the antigen before, the b-cells are now stimulated to divide by mitosis, these clones can then become memory cells or plasma cells.


thats correct :biggrin:
Do we need to know how microorganisms enter the body or just how they cause disease (produce toxin + damage host tissue)?

Also if anyone has any notes on vaccination, it would be appreciated. :smile:
(edited 12 years ago)
Original post by Mocking_bird
Do we need to know how microorganisms enter the body or just how they cause disease (produce toxin + damage host tissue)?

Also if anyone has any notes on vaccination, it would be appreciated. :smile:


Pathogens include bacteria, viruses and fungi.

Disease can result from pathogenic microorganisms penetrating any of an
organism’s interfaces with the environment. These interfaces include the digestive
and gas-exchange systems.


Pathogens cause disease by damaging the cells of the host and by producing
toxins.


According to the specification, it would be useful to know such things.
Original post by Mocking_bird
Do we need to know how microorganisms enter the body or just how they cause disease (produce toxin + damage host tissue)?

Also if anyone has any notes on vaccination, it would be appreciated. :smile:


I think we need to know that they can enter by like nose mouth ears etc...

But it's mostly common sense
Original post by stoppy123
I think we need to know that they can enter by like nose mouth ears etc...

But it's mostly common sense


Pathogens include bacteria, viruses and fungi.

Disease can result from pathogenic microorganisms penetrating any of an
organism’s interfaces with the environment. These interfaces include the digestive
and gas-exchange systems.


Pathogens cause disease by damaging the cells of the host and by producing
toxins.


According to the specification, it would be useful to know such things.
Any notes on Pulmonary TB? I know it's destroys alveoli when it's active and can then spread by the blood, but what happens in it's passive phase?
Reply 1394
Original post by crazycake93

Original post by crazycake93
Did not expect it to come up again, ignored the whole topic.

scraped 81ums in that paper, good thing i got 138/140 in unit 2 eh :tongue:


heh!
i hope that is a lesson for u now, innit?
good u made it in unit 2 well done!
Original post by Cherry Coke
I've already failed this exam once. :colonhash: Defo going to fail it again.


I've failed it twice so if I mess up this time I will not be happy :/ fml
questions on immunity :biggrin:

1) define monoclonal antibodies (1)
2) state two barriers which prevent the entry of pathogens (2)
3) explain the process of phagocytosis (5)
4) Describe the role of memory cells in the immune response (4)
5) where do B lymphosytes mature? (1)
6) state two difference between T and B cells (2)
7) state and explain the two types of immunity (4)
9) Give two reason why the control of cholera by vaccination is difficult? (2)
10) Give two ethical issues associated with vaccination programmes (2)

whoever answers these question first makes their own batch of questions :biggrin:
Original post by maria-95
questions on immunity :biggrin:

1) define monoclonal antibodies (1)
2) state two barriers which prevent the entry of pathogens (2)
3) explain the process of phagocytosis (5)
4) Describe the role of memory cells in the immune response (4)
5) where do B lymphosytes mature? (1)
6) state two difference between T and B cells (2)
7) state and explain the two types of immunity (4)
9) Give two reason why the control of cholera by vaccination is difficult? (2)
10) Give two ethical issues associated with vaccination programmes (2)

whoever answers these question first makes their own batch of questions :biggrin:


1) antibodies produced from cloned b-cells
2) Skin and not sure. I'll just guess tears :/
3) pathogen attracts a phagocyte. The phagocyte engulfs the pathogen forming a vescile around it. Releases digestive enzymes from the lysosomes than hydrolyse the pathogen. Presents it's antigens on it's cell surface membrane to stimulate production of T-cells.
4) They remain in the body for a long time incase of a second infection. They remember the antigens so the immune system skips straight to the specific respsonse. Produces antibodies faster so symptoms don't appear.
5) Bone marrow
6) T-cells stimulate production of B-cells and B-cells produce antibodies.
7) Active immunity. Antibodies created by your own system so is long lasting. Passive immunity. Antibodies transferred from an external environment. Short term as no B-memory cells.
8) Water borne disease and easily transmitted?
9) In herd immunity not everyone needs to be vaccinated so some people will feel it is unfair others don't have to. Use of animals as test subjects.
Reply 1398
Original post by maria-95

Original post by maria-95
questions on immunity :biggrin:

1) define monoclonal antibodies (1)
2) state two barriers which prevent the entry of pathogens (2)
3) explain the process of phagocytosis (5)
4) Describe the role of memory cells in the immune response (4)
5) where do B lymphosytes mature? (1)
6) state two difference between T and B cells (2)
7) state and explain the two types of immunity (4)
9) Give two reason why the control of cholera by vaccination is difficult? (2)
10) Give two ethical issues associated with vaccination programmes (2)

whoever answers these question first makes their own batch of questions :biggrin:


1)monoclonal antibodies are single clones onf antibodies made by B-lymphocytes
2)skin, HCl in the stomach
3)phagocytosis is when a phagocyte detects a foreign pathogen, the phagocyte releases chemicals to attract the pathogen, the phagocyte attach themselves to the surface of the pathogen, then the phagocyte engulfs the pathogen and forms a vesicle, lysosmes produce digestive enzymes and fuse with the phagocyte and the digestive enzymes break down the pathogen, and then the useful chemicals are absorbed by the cytoplasm and the unuseful product are later egested by the body.
4)they memorise the antigens on the surface of a pathogen and responds for future infection
5)bone marrow
6)T cells are involved in the cell mediated immunity, while b cells are involved in the humoral immunity
7)passive immunity, the antibodies are already made, and there is active immunity, the antibodies are made by the body
8)that is because there are different starins of cholera and it is hard to control when it is spread all over the body, and there is antigenic variability
9)religious people might be agains animal testing, or some people might be scared to take vaccinations as they are not tested or not approved by known companies
Original post by maria-95
questions on immunity :biggrin:

1) define monoclonal antibodies (1)
2) state two barriers which prevent the entry of pathogens (2)
3) explain the process of phagocytosis (5)
4) Describe the role of memory cells in the immune response (4)
5) where do B lymphosytes mature? (1)
6) state two difference between T and B cells (2)
7) state and explain the two types of immunity (4)
9) Give two reason why the control of cholera by vaccination is difficult? (2)
10) Give two ethical issues associated with vaccination programmes (2)

whoever answers these question first makes their own batch of questions :biggrin:


1) Many Identical antibodies produced in a single clone from the same b-cell.
2) Skin and Mucus
3) Phagocytes detect the pathogen by the chemicals it gives off. The phagocyte engulfs the pathogen in a vesicle, which a phagosome then forms around. Lysosomes fuse with the phagosome and release lytic enzymes into the phagosome breaking down the pathogen. The break down products are digested by the phagocyte and indigestable products are released.
4) Exposure to a specific antigen on a b cells surface membrane results in b cells possessing the complimentary antibody to divide by mitosis, some of these can then become memory b cells. The memory b cells circulate in the blood and if you come into contact with the same pathogen, the memory b cell will divide and rapidly produce antibodies which have a specific tertiary structure complimentary to the antigen, and will bind to it forming an antibody-antigen complex and thus destroying it.
5) Wut.
6) T cells have receptors on their surface, B cells have antibodies.
T cells are the cell mediated response, B cells are the humerol response.
7) Passive - the individual is given an injection of the antibodies as opposed to their own immune system being able to divide and produce the plasma cells which possess the complimentary antibody - doesnt last long as memory b cells arent produced.
Active - The individuals own immune system creates the antibodies by the division of b cells which possess the complimentary antibody and memory b cells are made.
9)Cholera has a high mutation rate and erm.. i dont know.
10) Tests on animals - unethical.
Some people in deprived areas may not recieve the treatment.
^ Guesses.



Fingers crossed this is better than my results in the last immunity questions >_<

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