Copyright
©The Author(s) 2015.
World J Stem Cells. Jan 26, 2015; 7(1): 51-64
Published online Jan 26, 2015. doi: 10.4252/wjsc.v7.i1.51
Published online Jan 26, 2015. doi: 10.4252/wjsc.v7.i1.51
Table 1 Summary of seddon and sunderland classifications following peripheral nerve injury adapted from[98]
Sunderland | Seddon | Injury | Neurosensory impairment | Recovery potential |
I | Neuropraxia | Intrafascicular oedema, conduction block Segmental demyelination | Neuritis, paraesthesia Neuritis, paraesthesia | Ful (1-7 d) Full (1-2 mo) |
II III IV | Axonotmesis | Axons severed, endoneurial tube intact Endoneurial tube torn Only epineurium intact | Paraesthesia, episodic dysesthesia Paraesthesia Hypoaesthesia, dysaesthesia neuroma | Full (2-4 mo) Slow, Incomplete (12 mo) Neuroma |
V | Neurotmesis | Loss of continuity | Anaesthesia, extreme pain and neuroma formation | None |
VI | As per V | As per V | Nil |
Table 2 Table of various neuron markers their distributions and function adapted from[99]
Marker | Distribution | Protein function |
GFAP | Mature cells of glial origin | Specifically found in astroglial cells |
MAP 2 | Mature marker of neurones | Thought to be involved in microtubule assembly during neurogenesis |
Nestin | Developing nervous system, myogenic, endothelial and hepatic cells | Intermediate filament protein expressed in multiple tissues |
NF-70 | Most PNS neurones | Structural protein supporting large axons and synapses |
NSE | Early neuronal marker | Three variants: α, β, γ with only the γ isoenzyme expressed in neuronal tissue |
S100 | Cytoplasm of SCs, astrocytes and astrogliosis | Non-specific cell marker involved in multiple cell processes including cell cycle progression and differentiation |
Synaptophisin | Brain synaptic vesicles | Directs vesicle associated membrane protein-2 to intracellular compartments |
TAU | Axons | βNeuronal microtubule associated protein stabilising microtubules and link to signalling pathways to cytoskeleton |
βIII-tubulin | Central and peripheral nervous system axons | β tubulins heterodimerize to form microtubules involved in axon guidance |
Table 3 Comparision the different methods of chemical differentiation of adipose derived stem cells
Nerve differentiation chemicals | Histochemical markers positive | Ref. |
B27/bFGF/EGF | MAP2, β-III tubulin, S-100, GFAP, Nestin, | [19,21,42-45,47] |
IBMX/dexamethasone/insulin/indomethacin | S100, GFAP | [94] |
β-mercaptoethanol/butylated hydroxanisole/retinoic acid/EGF/bFGF | GFAP, Nestin, β-III tubulin, NSE, TAU, MAP2 and Synaptophisin | [40] |
β-mercaptoethanol/retinoic acid/PDGF/bFGF/forskolin/GGF-2 | GFAP, S100 | [41,58,59,95] |
Table 4 Animal studies modelling adipose derived stem cells and conduits for peripheral regeneration
Animal models | Details | Measured outcomes | Ref. |
Rat | Polycaprolactone conduit for 6 mm nerve gap | SNI, nerve thickness | [56] |
Rat | Fibrin conduit 10 mm nerve gap | Axon regeneration | [42] |
Rat | Polyhydroxybutyrate conduit 10 mm nerve gap | Axon regeneration | [59] |
Mouse | Nerve crush model and local administration ADSC ± matrigel | Axon regeneration | [48] |
Rat | Decellularised vascular conduit v autogenous nerve and vascular conduits containing ADSC | Axon regeneration, nerve conduction velocity | [90] |
Rat | Silastic conduit for 13 mm nerve gap | SNI, EPT, sensory nerve function | [57] |
Rat | Silicon conduit ± collagen or ADSCs | Axon regeneration, nerve conduction velocity | [100] |
Rat | Nerve crush model with systemic injection of ADSC | Axon regeneration, motor recovery | [68] |
Rat | Genipin-Gelatin-Tricalcium phosphate conduit 10 mm nerve gap | SNI | [92] |
Rat | ADSC injected into repaired chronic denervated nerve | Axon regeneration, PFI | [89] |
Rat | Microporous conduit for 15 mm nerve gap | Motor recovery | [60] |
Rat | Fibrin conduit for 10 mm nerve gap | Motor recovery, GAP-43 expression in dorsal root ganglion | [58] |
Dog | Polytetrafluoroethylene tube and alginate hydrogel l 7 mm nerve gap | Axon regeneration | [51] |
- Citation: Zack-Williams SD, Butler PE, Kalaskar DM. Current progress in use of adipose derived stem cells in peripheral nerve regeneration. World J Stem Cells 2015; 7(1): 51-64
- URL: https://www.wjgnet.com/1948-0210/full/v7/i1/51.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v7.i1.51