Neural Tissue Engineering, by Jonathan Hummel

Nerve Tissue Damage

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

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 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 or loss of productivity, not to mention discomfort, in those effected.[5]

Summary of Neural Tissue Engineering History

• 1965 : Someone did something

Methods of Neural Tissue Repair

In the Peripheral Nervous System

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Recent Advances and Future Directions

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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.

• [5] http://jnnp.bmj.com/content/63/suppl_1/S19.full

• [6] http://www.brainandspinalcord.org/recovery-traumatic-brain-injury/cost-traumatic-brain-injury/index.html

• [7] http://www.alz.org/facts/overview.asp