Genome Complexity; amazing immune system (Introduction)

by David Turell , Monday, November 21, 2016, 18:24 (2924 days ago) @ David Turell

Another study into how T cells recognize foreign material when surrounded by a welter of 'self' proteins:

http://medicalxpress.com/news/2016-11-immune-receptors-amplify-invader-mini-machines.html

"When a receptor on the surface of a T cell—a sentry of the human immune system—senses a single particle from a harmful intruder, it immediately kicks the cell into action, launching a larger immune response. But exactly how the signal from a single receptor, among thousands on each T cell, can be amplified to affect a whole cell has puzzled immunologists for decades.

"Now, Salk scientists have discovered the key to the amplification of an "invader" signal. The T cell receptor that detects the intruder turns into a mini-machine, activating and releasing copy after copy of a protein called ZAP70.

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"T cells are central in the adaptive immune response, which is the body's ability to recognize pathogens and respond to them. A single T cell's receptors screen thousands of molecules at any given second, but most of them originate from the body's own proteins and have to be ignored as "self." Researchers have struggled to explain how, in the wake of overwhelming "self" signals, a T cell can detect and respond to one or two "invader" signals.

"Lillemeier's lab studied ZAP70, a protein that associates with T cell receptors and becomes activated when the receptors recognize a foreign molecule. To track the activity and location of ZAP70 molecules, the team tagged them with a fluorescent marker while anchoring each T cell receptor in place. To the group's surprise, ZAP70 molecules were being activated by the T cell receptors and then moving away, spreading throughout the cell.

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"By churning out ZAP70 and sending it throughout the cell—as opposed to just activating a handful of ZAP70s and keeping them tethered to the T cell receptor—the immune cells can rapidly spread a signal throughout the cell.

"'What we saw is that at the beginning of signaling, you have lots of ZAP70 being released from the T cell receptor to amplify and distribute the signal," says Lillemeier. "But once the signaling is established, the T cell receptor actually adapts and stops releasing so much of ZAP70."

"Questions remain on how the process works, including what the ultimate destinations of the ZAP70 molecules are and how they go on to transmit signals. But the observation, Lillemeier says, is progress toward understanding how T cells identify and react to pathogens.

"'It's really important to understand this process since T cells are at the center of the adaptive immune response," he says. "If the receptors are not controlled well, you're sick; you might either have an autoimmune disease or you can't respond to infections." Being able to make the receptors have a stronger or weaker signal—perhaps by changing how much ZAP70 they activate and release—could help treat these kinds of diseases, he adds." (my bold)

Comment: This is an automatic cellular reaction, no thought involved. The researchers are now looking for the feedback mechanism to control the reaction, a must in all the biochemistry of life. Not by chance.