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Some consequences of pre-BCR signaling:

a) Cell proliferation, differentiation, apoptosis, gene rearrangement, receptor editing, anergy
b) Phagocytosis, exocytosis, endocytosis, chemotaxis, pinocytosis, mitosis
c) Active transport, passive transport, osmosis, diffusion, filtration, facilitated diffusion
d) Transcription, translation, replication, mutation, recombination, splicing

User RGO
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1 Answer

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Final answer:

Pre-BCR signaling initiates various cellular responses like protein expression, cellular metabolism, and cell division, depending on the type of cell and environmental factors. Examples include Epidermal Growth Factor (EGF) affecting protein expression, MAP-kinase cascade for cellular metabolism, and FAS-RAS signalling for cell division.

Step-by-step explanation:

Pre-BCR signalling is crucial in the development and functionality of B cells within the immune system. After the ligand binds to the cell-surface receptor, this initiates a signalling pathway or cascade that causes a variety of responses in the cell, depending on its type and the internal and external environment.

For instance, an effect on protein expression can be exemplified by the binding of Epidermal Growth Factor (EGF) to its receptor tyrosine kinase. When it comes to cellular metabolism, the MAP-kinase cascade illustrates how signaling can impact this aspect of cellular function. Lastly, for cell division, the FAS-RAS signalling pathway serves as an example of how signaling can regulate cellular proliferation.

Each of these pathways can lead to different cellular responses like cell proliferation, differentiation, apoptosis (programmed cell death), gene rearrangement, receptor editing, and energy storage or utilization within the cell, influences that are vital for both multicellular and unicellular organisms.

User Keith Banner
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