Chemical signaling is the process by which cells communicate with each other.
This is a foundational concept for understanding how different organ systems coordinate their activities in the body.
Builds upon knowledge from biology 226 (nervous system and neuron communication).
Chemicals act as messaging substances, similar to letters carrying information.
The message must physically reach the recipient cell.
This topic covers various subtopics related to cell-to-cell communication and involves conceptual physiology.
Chemical messenger molecules flow directly from one cell to another.
Cells must be physically connected via protein structures called gap junctions.
Gap junctions create a pore or tunnel allowing substances to pass between cells.
The direction of flow is determined by the concentration gradient of the chemical.
Substances shared include ions (sodium, calcium, potassium, chloride) and small molecules (glucose, amino acids).
Gap junctions consist of multiple proteins forming a ring (connexon).
Pore is much larger than channel proteins which only allow molecules as big as water through.
Chemical messenger molecules are released from a secretory cell into the extracellular fluid (ECF).
The chemical then travels through the ECF to reach the target cell.
Target cells possess receptor molecules, usually proteins, that bind to the chemical messenger.
Binding of the messenger changes the receptor's shape (conformation) and activates it.
Activation triggers a chemical chain reaction inside the target cell, leading to a desired response.
To stop the response, the messenger must be removed from the receptor, reverting it to its inactive form.
Receptors are highly specific to particular messenger molecules based on their shapes.
The messenger's shape must complement the binding site on the receptor.
A given receptor is typically activated by only one or two different messengers due to the precise structural requirements.
Computer-generated models illustrate the complex shapes of hormones like human growth hormone and the corresponding receptor, emphasizing the near-perfect match required for binding.
The messenger must be removed from the receptor to deactivate it.
The most common method is enzymatic breakdown of the messenger.
Example: Acetylcholine (ACH) in a chemical synapse is broken down by an enzyme.
The enzyme is often associated with the target cell's membrane, with its active site facing the extracellular fluid (e.g., synaptic cleft).
For messengers like hormones that travel long distances through the bloodstream, enzymes in the liver and kidneys break them down.
The body uses three methods to control when a chemical signal is released: humoral, neural, and hormonal.
A substance in the extracellular fluid (a "humor") influences the release of a chemical signal.
Example: Parathyroid glands monitor blood calcium levels. If calcium is too low, they release parathyroid hormone (PTH).
A neuron tells the secretory cell what to do.
Example: Sympathetic neurons stimulate the adrenal medulla to release catecholamines (hormones involved in the fight-or-flight response).
A hormone tells the secretory cell what chemical signal to release.
Example: The pituitary gland releases hormones that tell other glands (e.g., thyroid, adrenal cortex) to release their hormones.
Chemical signals exhibit different patterns of secretion over time: chronic, acute, and cyclic.
Fairly steady maintenance of chemical signal levels over time.
The level hovers around a set point, with only small deviations.
Example: Thyroid hormones, which maintain basal metabolic rate.
Responds to a particular stimulus or change in the body and are secreted to make a correction.
Short-lived, ceasing when the stimulus is removed.
Example: Epinephrine (adrenaline) is released in response to stress (physical or psychological) and stops when the stressor is removed.
Rises and falls in a fairly predictable pattern over time.
Example: Female reproductive hormones, such as estrogen, fluctuate across the monthly menstrual cycle.