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APCModerator: BioTeam
18 posts • Page 1 of 2 • 1, 2
APChello I have FEW questionS
1.A virus normally is inside a cell...how does the antigen PRESENTING CELL recognise it?? according to how much i know,it needs to recognize the MHC class II to trigger signal for the Th cell to release cytokines...which is a very primary need of the immune response....BUT HOW?? 2.Also APC cells internalize the antigen(a virus/anythin) either by phagocytosis or endocytosis....what does this mean ...as in does the virus get phagocytosed with the cell it flourishes in...how does it escape the phagolysosomal phase.......and also what exactly is the difference between endocytosis and phagocytosis...
1. Free virus can be arrested by APC but other can be already infiltrated another cells, this condition is taken control by presenting viral antigen by the infected cell (because virus infiltration and replication already changed the cell's surface antigen). The infected cell will also as APC to the specific immune system and the result is: cytotoxicity will occur in that infected cell.
2. Phagocytosis is an endocytosis process done by Phagocytes.. Some virus have a special ability based on their morphological, physiologycal and biochemistry aspects...so, if they can escape from endolysosomic process, don't be too surprised for that thing.. Q: Why are chemists great for solving problems?
A: They have all the solutions.
Actually there are a lot of differences between phagocytosis and endocytosis. One involves mainly polimerisation of actin molecules outwards while the other involves polimerisation of clatrin molecules inwards... And a lot of other things, which would be useless to post here...
However, to my surprise, Neil Campbell classifies phagocytosis as a type of endocytosis in BIOLOGY 7th edition "I have no intention of stopping anytime soon. I want to understand the universe and answer the big questions, that is what keeps me going" - Stephen Hawking
Re: APC
A virus-infected cell will present modified peptide via MHC-I on its surface. This will attract CTL to kill the cell. MHC-II is for recognizing external pathogens, MHC-I is for internal pathogens.
Antigen is internalized and processed to break up into peptide. Then, the peptide will be externalized to present to T-Cell via MHC-I or MHC-II. ![]()
@victor
Poetry is for literature people. We aim to break down and understand, not simplify and memorise(well, Poison's teachers do from what she told us "I have no intention of stopping anytime soon. I want to understand the universe and answer the big questions, that is what keeps me going" - Stephen Hawking
how does APC recognise the intracellular viral antigens (peptides or dna/rna)?
before the intracellular viral antigens can bind to MHC class I, some kind of receptors have to bind to the antigens first rite? Recently, my classmate presented a topic that mention that some APCs expressed TLR3 intracellularly. This TLR3 can then bind to the intracelluar viral dsRNA.. wondering if there are any receptors that can bind to antigen intracellularly? and also how does the virus break out from the endosome after it has been engulf by the cell?? Go as far as you can see, and when you get there you will always be able to see farther.
they fuse their capsids with the endosome and release their genetic materials.. Q: Why are chemists great for solving problems?
A: They have all the solutions.
For APCs, it is not necessary to recognize whether it is pathogenic or nonpathogenic material. Their job is to process antigens that coming inside our body as much as they can, and present them as peptide with appropriate MHC to T-cell that will recognize and determine whether it is pathogenic or nonpathogenic material. It is T-cell job to take action whether we will generate immun response or immune tolerance.
We have three professional APCs i.e. dendritic cells (DC), macrophage (MΦ) and B-cell. As you may know, in innate immunity DC and MΦ have a job to engulf nonspecific antigens by pattern recognition, via FcR (Fc reseptor), complement system, etc. Here, to bridge between innate and adaptive immunity, after engulf antigen, they will process and externalize them to be presented with appropriate MHC. B-cell has a BCR (B-cell receptor, similar as Ig but bound on the surface of B-cell) to bind specific antigens and then internalize and externalize with the same mechanism as the former two APC. Virus-infected cell can also act as APC to present viral antigens after with MHC-I (new-made).
Oh a nice topic! Very nice! I never read about this before. If you don't mind, could you please send me the paper please? I'll be more than happy to get it. Thanks in advance However, since this is new to me, I try to digest your question. I am a bit confused to this question. TLR3 is an internal receptor for virus. If this TLR3 is a family of Toll-like receptor, means that it will bind nonspecifically to virus before it comes into nucleus to hijack infected-cell's DNA. In cytoplasm there is a giant protein complex known as proteasome that will cut viral protein into peptides. After some steps of reaction (if you need this in detail, I'll explain it later, this is a bit complicated), eventually the peptide will bind to newly synthesized MHC-I and externalize to be presented to T-cell. So.. that's it. Is this what you want to know or...?
Is virus engulfed and trapped in endosome? I am not sure FOR ALL: I have a nice figure of MHC-I and MHC-II generation. If you think you will understand with this caricature, you can save it; if not then just leave it MHC class I:
MHC clas II:
For myself they are grrreat figures, explain me a lot of things in funny ways ![]()
some types of viruses can send their capsides along with their genetic material via endosome..(usually for the lipid enveloped virus). It's due to prevent the Viruses' genetic material from nuclease inactivation in cytoplasm. Q: Why are chemists great for solving problems?
A: They have all the solutions.
Ah ya, true. By covering their 'body' in lipid envelope, they can diffuse cell membrane easily and slap! they come inside the cell and ready to hijack it. Thanks for reminding me this mechanism, my dear
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18 posts • Page 1 of 2 • 1, 2
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