Neural Tissue Engineering, by Jonathan Hummel: Difference between revisions

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As described earlier, the mechanisms of response to damage in the CNS and PNS are dramatically different and thus prose different challenges in the field of tissue engineering.[2] While there is a long way to go in expanding the treatment options for both parts of the nervous system, there are many more methods of repair that have been developed to address problems of the PNS:
As described earlier, the mechanisms of response to damage in the CNS and PNS are dramatically different and thus prose different challenges in the field of tissue engineering.[2] While there is a long way to go in expanding the treatment options for both parts of the nervous system, there are many more methods of repair that have been developed to address problems of the PNS:
=== In the Peripheral Nervous System ===
=== In the Peripheral Nervous System ===
[[Image:Cap.PNG|thumb|center|upright=2.0|alt=Various treatment strategies for nerve injuries in the PNS [8]| Various treatment strategies for nerve injuries in the PNS [8]]]
[[Image:Cap.PNG|thumb|center|upright=4.0|alt=Various treatment strategies for nerve injuries in the PNS [8]| Various treatment strategies for nerve injuries in the PNS [8]]]





Revision as of 21:13, 12 April 2015

Nerve Tissue Damage

Different responses to damage in the peripheral and central nervous system [1]
Different responses to damage in the peripheral and central nervous system [1]
Central and peripheral nervous system [3]
Central and peripheral nervous system [3]

Damage to nervous tissue in both the central (CNS) and peripheral (PNS) nervous system arises from a wide variety of causes. Direct mechanical trauma, inadequate blood supply, or failure of the cellular machinery of the neurons themselves can result in the severing of axons, damage of neuron cell bodies, or disruption of existing synapses.[1] While all three types of nerve tissue damage are interconnected, the repair of severed axons has historically received the most study, largely due to the fact that the prospects of recovery are much better in the absence of extensive cell body damage or synapse obstruction by aggregates.[1][2] Regardless of the initial cause, the response to axon damage by the local cells in neural tissues differ dramatically between the CNS and PNS, resulting in different challenges when developing treatments.[1] Glial cells, or more specifically Schwann cells, are the cells responsible for forming the myelin sheath that surrounds, protects, and nourishes the axons of neurons.[2] Shortly after the disruption of an axon in the PNS, macrophages are attracted to the area to swiftly remove the cellular debris of the Schwann cells, as well as any debris from the damaged axon itself. Damage of the axon triggers the cell body associated with that axon to express a variety of genes associated with the production of axon components as well as elongation. Surviving Schwann cells in the area proliferate and reorganize into a linear supporting structure. They also release growth factors and proteins that guide the direction in which the growth cone of the extending axon moves. This ensures that the extending axon moves toward the appropriate target neuron or tissue to repair communication.[1] In the CNS, the response to the exact same axon damage results in a different course of events that are much less favorable for tissue repair. The cellular debris are not cleaned up nearly as rapidly as they are in the PNS and persist for weeks, rather than days, which poses obstacles for axon extension and reformation of myelin structures. On top of that, expression of genes associated with axon repair rarely occurs in CNS neurons the way it does in the PNS. When axon extension is initiated by a CNS neuron, proper function of the growth cone is inhibited by factors released by oligodendrocytes, the CNS equivalent of the Schwann cells. Another type of glial cell, called astrocytes, release other factors in response to axon damage that inhibits the extension of the axon.[1] Thus, in the PNS there are mechanisms that actively promote the repair of damaged neural tissues, while in the CNS there are mechanisms in place to actively prevent the repair of neural tissues. The goal of neural tissue engineering is to restore lost neural tissue function by using engineered cells and/or materials. The strategies behind tissue engineering in CNS and PNS tissues are thus very different, and as one can imagine, there has been much more success in the PNS because preexisting repair mechanism simply need to be aided.[2] It should also be mentioned that other sources of nerve tissue damage, such as degenerative diseases like Alzheimer's, do not result in direct axon damage but a buildup of proteins and aggregates that impede proper neural function. Thus, approaches to treatment of these malfunctions are very different and further understanding of these disorders is required.[4]

Economic and Societal Impact

The exact costs associated with nerve tissue damage are difficult to estimate, largely due to the fact that there are such a wide variety of neurological disorders and traumas, some of which are not fully understood or are under the realm of psychology and/or psychiatry.[5] That being said, the costs both economically and emotionally that stem from nerve tissue damage are surely noteworthy. To get a sense for the economic impacts, one can look at the costs associated with any individual health issue related to nerve tissue damage or malfunction. For example, the overall annual cost of traumatic brain injuries in the United States is estimated to be $48.3 billion and the lifetime cost of caring for a traumatic brain injury survivor is estimated to be between $0.6 and $1.9 million.[6] The costs associated with degenerative diseases are even larger, with a projected $226 billion to be spent due to Alzheimer's in 2015.[7] Especially in the case of nerve tissue damage and disease, the emotional and quality of life impacts are just as important as the economic effects. Damage and degeneration of nerve tissues in the PNS often result in the pain, loss of feeling, and loss of control in the affected parts of the body. These symptoms result in varying degrees of disability and loss of productivity in those affected, not to mention general discomfort.[5] In nerve tissue damage and degeneration that affects the CNS, the greatest losses are often in cognition and the ability to normally interact with family or friends. In the case of CNS degeneration, even before the more grave effects set in, there is often a level of fear and pain associated with the prospect of losing cognition or control, which also cannot be overlooked.[5] What is often most discouraging for those affected by neurological damage or degeneration is the lack of effective treatment to solve or combat these problems. This is largely due to a massive knowledge gap with regards to the nervous system and the specific causes of disorders and modes of repair.[5][2] While the field of neural tissue engineering is currently only able to address simple PNS damage, further study of tissue engineering in both the PNS and CNS could someday lead to solutions to even the most complex and detrimental neurological degenerative diseases.

Summary of Neural Tissue Engineering Progress

The following timeline is hardly an exhaustive list of the key events in the history of neural tissue engineering. It does, however, provide a general summary of the progression of this field over time:

  • 1543-1627 : Gabriele Ferrara developed and described a procedure for connecting severed nerves with gentle sutures and limb immobilization.[2]
  • 1954 : Use of autologous nerve graphs for peripheral nervous system repair, which was developed during WWII, is formally published as a method of repair.[2]
  • 1972 : Methods of nerve repair further are improved with use of the operating microscope and understanding of the negative effects of suture tensions on nerve healing.[2]

Methods of Neural Tissue Repair

As described earlier, the mechanisms of response to damage in the CNS and PNS are dramatically different and thus prose different challenges in the field of tissue engineering.[2] While there is a long way to go in expanding the treatment options for both parts of the nervous system, there are many more methods of repair that have been developed to address problems of the PNS:

In the Peripheral Nervous System

Various treatment strategies for nerve injuries in the PNS [8]
Various treatment strategies for nerve injuries in the PNS [8]


In the Central Nervous System

Recent Advances and Future Directions

Stuff goes in here...

References

  • [1] Zhang, Lijie, Jerry Hu, and Kyriacos A. Athanasiou. “The Role of Tissue Engineering in Articular Cartilage Repair and Regeneration.” Critical reviews in biomedical engineering 37.1-2 (2009): 1–57. Print.
  • [1] Recovery from Neural Injury
  • [2] Peripheral nerve regeneration: Experimental strategies and future perspectives
  • [3] CNS/PNS photo
  • [4] Senile plaque neurites in Alzheimer disease accumulate amyloid precursor protein.
  • [8] Peripheral nerve conduits: technology update