5.10: Touch- The Skin

Resources

• Glossary terms
• Key Takeaways
• Test Yourself
• Additional Review

Touch can come in many forms: pressure, vibration, stretch, motion, edges, points, etc. Receptors in the skin allow for perception of these different characteristics, and when this information is combined in the central nervous system, we are able to determine the location, strength, duration, movement, shape, and texture of the object interacting with the skin.

Cutaneous (meaning found in the skin) mechanoreceptors are responsible for sensing mechanical changes to the skin.

Receptors

We can feel different modalities of touch because of the presence of specialized sensory receptors, called mechanoreceptors, located in the skin.

There are four different classes of cutaneous mechanoreceptors. These different mechanoreceptors have slightly different shapes and are therefore capable of detecting different types of stimuli.

1. Merkel’s discs are located at the border between the dermis and epidermis and are specialized to detect edges and points. They are very densely populated underneath our fingertips. These are the most precise mechanoreceptors with resolution at the level of 0.5 mm, which allow us to detect different distances in bumps while running your fingers across Braille.
2. Pacinian corpuscles are mechanoreceptors wrapped in several layers of connective tissue. The Pacinian corpuscles are located deep in the dermis of the skin and are responsible for perception of vibrations.
3. Meissner’s corpuscles are located in the epidermis layer and are highly concentrated at the fingertips. They are stimulated by skin motion/movement.
4. Ruffini endings are located in the dermis layer of the skin and respond to stretching of the skin.

Figure 37.1. The different mechanoreceptor types are located in different regions of the skin and are responsible for perception of different characteristics of a touch timulus. Pacinian corpuscles and Ruffini endings are located deep in the dermis. Meissner corpuscles are located in the dermis near the epidermis, and Merkel cells are located in the epidermis, near the surface of the skin. ‘Mechanoreceptors’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Structure of a Cutaneous Mechanoreceptor

The somatosensory afferents from the cutaneous mechanoreceptor have their cell bodies located in the dorsal root ganglion (DRG), a clump of somata that are close to the dorsal side of the spinal cord. These touch receptors are the primary neurons and are classified as pseudounipolar neurons based on their morphology. Pseudounipolar neurons don’t have true dendrites; instead each soma sends a single protrusion which branches into two directions. One branch goes towards the skin surface where it terminates as one of the mechanoreceptors. Typically, the terminal of this branch is surrounded by a connective tissue covering. The other branch off the soma travels towards the spinal cord.

Figure 37.2. Cutaneous mechanoreceptor structure. Cutaneous mechanoreceptors have their cell bodies located within the dorsal root ganglion. These pseudounipolar neurons have a singular projection from the cell body that branches, with one branch traveling out to the skin. The axon terminal is surrounded by a layered connective tissue covering (capsule). The other branch travels to the spinal cord. ‘Cutaneous mechanoreceptor structure’ by Valerie Hedges is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

Sensory Transduction

On a molecular scale, these mechanoreceptors detect changes at the skin using mechanically-gated ion channels. In previous chapters we discussed ion channels that are gated by voltage changes and channels that are gated by neurotransmitters. In the somatosensory system, we find ion channels that are gated by physical distortion or stretch of the membrane. These transmembrane proteins are specialized for detecting the physical distortion of the channel and can open by stretch of the membrane itself or indirectly through movement of intra- or extracellular proteins that are linked to the channels. They are specialized for detecting the physical distortion of the channel, similar to the channels found in the stereocilia of the hair cells or vestibular cells.

When pressure is applied to these proteins, the cation channel opens and sodium and calcium flow down their electrochemical gradient into the neuron, causing both a depolarization and the initiation of second messenger cascades. This depolarization is referred to as a ‘receptor potential’. If enough stimulus is applied, the depolarization reaches threshold potential for the cell and an action potential is sent toward the spinal cord.

 

Animation 37.1 Mechanoreceptors respond to touch stimuli via stretch-gated non-selective cation channels. The channels can either open due to stretch of the membrane itself which stretches open the channel or due to proteins associated with the channels that pull the channel open. ‘Stretch-Gated Ion Channels’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License. View static image of animation.

Receptive Fields

Each cutaneous mechanoreceptor is able to detect somatosensory information in an area of skin called the receptive field. When the receptive field is touched, the mechanoreceptor will be activated. The size of a receptive field can be determined by measuring the rate of action potentials from the nerve that collects somatosensory information from that patch of skin. The smaller the receptive field, the better the brain can distinguish between two different adjacent tactile stimuli.

Figure 37.3. Each mechanoreceptor will be activated by a specific region of skin, the receptive field. When no stimulation of the receptive field occurs on the surface of the skin, the mechanoreceptor will show a baseline firing rate. When stimulation of the receptive field occurs, the firing rate of the mechanoreceptor will increase. ‘Receptive Field Activation’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Receptive Field Size

Additionally, different classes of mechanoreceptors have different sizes of receptive fields: deeper structures, like Pacinian corpuscles, have larger receptive fields compared to receptors found closer to the skin surface that have smaller receptive fields.  Merkel cells and Meissner corpuscles, both of which are located near the skin surface, have small receptive fields and thus collect information from a restricted area of sensory space. Ruffini endings and Pacinian corpuscles, located deeper in the skin layers, have larger receptive fields than the Merkel cells and Meissner corpuscles and thus collect information over a large are of sensory space.

Figure 37.4. Receptive field sizes vary depending on the underlying mechanoreceptor type and location. Merkel cells and Meissner corpuscles have small receptive fields, whereas Pacinian corpuscles and Ruffini endings have large receptive fields. ‘Mechanoreceptor Receptive Fields’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Receptive field sizes are different among the different mechanoreceptors, but they also vary among different body regions. Even within one receptor type (e.g. Meissner corpuscles), receptive fields in regions like the fingers or lips are smaller than in regions like the back or leg. This allows us to have finer spatial resolution with locating and identifying objects using our fingers. The smaller receptive fields in these regions are a result of a higher density of receptors in the skin.

Figure 37.5. Density of mechanoreceptors can affect the size of the receptive field for each receptor. High density leads to smaller receptive fields. Density and receptive field size varies by location on the body. Regions like the hands and face have smaller receptive fields than regions like the back. ‘Receptive Field Location’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Two-Point Discrimination

Receptive field sizes are important because they allow us to locate a stimulus on our bodies. Larger receptive fields are not as precise as smaller receptive fields. One measure of receptive field size is two-point discrimination (try it at home!), which determines the minimum distance needed between two stimuli to perceive two separate points on the skin and not one. The hand has a smaller threshold for discerning between two points than does the back, a result of the different sized in receptive fields. In skin areas with a large receptive field, two adjacent stimuli may feel like one.

Figure 37.6. The size of the receptive fields affect the sensitivity of the skin, which can be measured by the two-point discrimination test. Tools like calipers or even a paperclip can be used to measure two-point discrimination. If the two points of the caliper feel like one point, they are both activating the same receptive field, indicating the receptive field is large. If, however, it is possible to perceive two separate points on the skin, then the calipers are activating two different receptive fields. ‘Two-Point Discrimination’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License.

Skin areas with small receptive fields are better able to distinguish two similarly-spaced points. The hand has a smaller threshold for discerning between two points than does the back, a result of the different sized in receptive fields.

The two-point discrimination threshold for the fingers is very small, which indicates that they have high sensitivity. Body areas with high sensitivity typically have higher density of mechanoreceptors, have receptors that have smaller receptive fields, and have more brain tissue devoted to processing the sensory information that comes from those structures.

The two-point discrimination threshold for areas such as the leg or torso is very large, which indicates that these areas have low sensitivity. Body areas with low sensitive have a lower density of mechanoreceptors, have receptors that have larger receptive fields, and have less brain tissue devoted to sensory information that comes from those structures.

Figure 37.7. 2-point discrimination thresholds across the body. 2-point discrimination threshold is the minimum distance between two points, typically measured in millimeters, needed to distinguish stimuli. The graph depicts the typical threshold to distinguish two points across various areas of the body. Areas such as the legs and stomach have high 2-point discrimination thresholds, indicating that they are less sensitive and that the two stimuli need to be placed further apart to distinguish two separate stimuli. Areas of the body like the hands and fingers have lowers 2-point discrimination thresholds, indicating that they are more sensitive and are capable to distinguishing two separate stimuli, even when very close in distance. ‘2-point discrimination across the body’ by Valerie Hedges is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

Adaptation Rate

Another important characteristic of the somatic sensory receptors is that of adaptation rate. The class of mechanoreceptors can be divided into two categories based on their electrical properties in response to stimuli: slowly adapting and rapidly-adapting.

Slowly-adapting mechanoreceptors change their action potential firing rate as long as the stimulus is present, while rapidly-adapting mechanoreceptors only change activity at the moment there is a change in stimulus. For example, imagine the stimulus of a coin that is sitting in the palm of your hand. The slowly-adapting sensory neurons may increase their firing rate as long as the coin is in your palm. When the quarter is removed, they return to their baseline firing rate.  Slowly-adapting mechanoreceptors change their action potential firing rate as long as the stimulus is present and are most useful for determining the pressure and shape of a stimulus. Merkel cells and Ruffini endings are both slowly adapting fibers.

 

Animation 37.2. Slowly adapting mechanoreceptors continuing firing action potentials throughout the duration of a stimulus. As the stimulus moves from not present, to weak, to strong, the action potential firing of the Ruffini ending fires throughout the entire stimulus. ‘Slowly Adapting Receptor’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License. View static image of animation.

Rapidly-adapting mechanoreceptors only change activity at the moment there is a change in stimulus, but not when a stimulus is constant. This firing makes rapidly adapting fibers specialized for detecting movement and vibration.  Considering the coin example from above, a rapidly adapting sensory neuron will change its action potential firing properties only at two timepoints: the moment the coin lands in your hand, and the moment that coin is removed. These neurons signal a change in status.

 

Animation 37.3 Rapidly adapting mechanoreceptors firing action potentials when the strength of the stimulus changes. As the stimulus moves from not present, to weak, to strong, the action potential firing of the Pacinian corpuscle only fires when the stimulus changes strength. ‘Rapidly Adapting Receptor’ by Casey Henley is licensed under a Creative Commons Attribution Non-Commercial Share-Alike (CC BY-NC-SA) 4.0 International License. View static image of animation.

Key Takeaways

• There are multiple types of mechanoreceptors in the skin that are activated by different types of touch stimuli
• The receptive field size differs among the types of mechanoreceptors
• The adaptation rate differs among the types of mechanoreceptors
• Receptive field is a region of skin that activate a given mechanoreceptor
• Receptive field size for a specific type of mechanoreceptor can vary in size across the body
• Mechanoreceptors express stretch-gated non-selective ion channels that depolarize the cell during sensory transduction

Test Yourself!

Additional Review

Describe the relationship between density of receptors, receptive fields, and two-point discrimination.

Answers

Attributions

1. Foundations of Neuroscience by Casey Henley. The original work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License
2. Open Neuroscience Initiative by Austin Lim. The original work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Media Attributions

• Mechanoreceptors © Casey Henley is licensed under a CC BY-NC-SA (Attribution NonCommercial ShareAlike) license
• somatosensory afferent © Valerie Hedges is licensed under a CC BY-NC-SA (Attribution NonCommercial ShareAlike) license
• Receptive Field Activation © Casey Henley is licensed under a CC BY-NC-SA (Attribution NonCommercial ShareAlike) license
• Mechanoreceptor Receptive Fields © Casey Henley is licensed under a CC BY-NC-SA (Attribution NonCommercial ShareAlike) license
• Receptive Field Location © Casey Henley is licensed under a CC BY-NC-SA (Attribution NonCommercial ShareAlike) license
• Two Point Discrimination © Casey Henley is licensed under a CC BY-NC-SA (Attribution NonCommercial ShareAlike) license
• 2 point discrimination © Valerie Hedges is licensed under a CC BY-NC-SA (Attribution NonCommercial ShareAlike) license