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Quantitative and morphological differences of nerve fibers between proliferative and mature scars in two-and three-dimensional spaces 被引量:5

Quantitative and morphological differences of nerve fibers between proliferative and mature scars in two-and three-dimensional spaces
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摘要 BACKGROUND: Numerous studies use fluorescent microscopy to obtain two-dimensional optical images of the morphology of nerve fibers in hypertrophic scars. In addition, current confocal microscopy studies have focused on normal, not pathological, cutaneous nerves. However, laser scanning confocal microscopy results in a three-dimensional structure of the nerve fibers. OBJECTIVE: To observe quantitative and morphological differences in nerve fibers from the proliferative and mature stage in hypertrophic scars using fluorescent and confocal microscopy. DESIGN, TIME AND SETTING: Neuropathological, comparison study was conducted at the Provincial Hospital Affiliated to Shandong University, China from June 2006 to July 2007. PARTICIPANTS: Specimens were selected from 30 patients undergoing scar restoration at the Provincial Hospital Affiliated to Shandong University of China at 1 month to 23 years following wound healing. The study comprised 20 males and 10 females. The scars were fibrous lesions, erythematous, tough, confined to skin lesions, did not exhibit ulceration or infection, exhibited telangiectasia, with or without itching and pain, and were not locally treated. Samples were equally assigned to two groups according to course of disease: proliferative group (〈 6 months) and mature group (6-24 months). Control samples were collected from full-thickness skin from donor sites (n = 10). METHODS: Nerve fiber morphology was observed using fluorescent and confocal microscopy following immunofluorescence of the skin specimens. The microscopic images were semi-quantitatively analyzed to acquire a positive area ratio of neurofilament protein-positive nerve fibers. MAIN OUTCOME MEASURES: Morphology and positive area ratio of neurofilament protein/positive nerve fibers was measured. RESULTS: The positive area ratio of neurofilament protein-positive nerve fibers was significantly greater in the proliferative group compared to the normal control group (P 〈 0.05). Nerve fibers were irregularly distributed and exhibited local swelling, twisting, and disconnection. However, the positive area ratio of neurofilament protein-positive nerve fibers was significantly less in the mature group compared with the normal control group (P 〈 0.05). The nerve fibers were arranged in an orderly manner, with intact inner and stereoscopic structures similar to normal skin. CONCLUSION: Compared with mature scars, hypertrophic scars exhibited a greater number of nerve fibers, with more serious pathologies. BACKGROUND: Numerous studies use fluorescent microscopy to obtain two-dimensional optical images of the morphology of nerve fibers in hypertrophic scars. In addition, current confocal microscopy studies have focused on normal, not pathological, cutaneous nerves. However, laser scanning confocal microscopy results in a three-dimensional structure of the nerve fibers. OBJECTIVE: To observe quantitative and morphological differences in nerve fibers from the proliferative and mature stage in hypertrophic scars using fluorescent and confocal microscopy. DESIGN, TIME AND SETTING: Neuropathological, comparison study was conducted at the Provincial Hospital Affiliated to Shandong University, China from June 2006 to July 2007. PARTICIPANTS: Specimens were selected from 30 patients undergoing scar restoration at the Provincial Hospital Affiliated to Shandong University of China at 1 month to 23 years following wound healing. The study comprised 20 males and 10 females. The scars were fibrous lesions, erythematous, tough, confined to skin lesions, did not exhibit ulceration or infection, exhibited telangiectasia, with or without itching and pain, and were not locally treated. Samples were equally assigned to two groups according to course of disease: proliferative group (〈 6 months) and mature group (6-24 months). Control samples were collected from full-thickness skin from donor sites (n = 10). METHODS: Nerve fiber morphology was observed using fluorescent and confocal microscopy following immunofluorescence of the skin specimens. The microscopic images were semi-quantitatively analyzed to acquire a positive area ratio of neurofilament protein-positive nerve fibers. MAIN OUTCOME MEASURES: Morphology and positive area ratio of neurofilament protein/positive nerve fibers was measured. RESULTS: The positive area ratio of neurofilament protein-positive nerve fibers was significantly greater in the proliferative group compared to the normal control group (P 〈 0.05). Nerve fibers were irregularly distributed and exhibited local swelling, twisting, and disconnection. However, the positive area ratio of neurofilament protein-positive nerve fibers was significantly less in the mature group compared with the normal control group (P 〈 0.05). The nerve fibers were arranged in an orderly manner, with intact inner and stereoscopic structures similar to normal skin. CONCLUSION: Compared with mature scars, hypertrophic scars exhibited a greater number of nerve fibers, with more serious pathologies.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2010年第2期132-137,共6页 中国神经再生研究(英文版)
关键词 SCAR HYPERTROPHIC neurofilament proteins INNERVATION nerve regeneration scar hypertrophic neurofilament proteins innervation nerve regeneration
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  • 1[7]Bentz K,Molcanyi M,Hess S,et al.Neural differentiation of embryonic stem cells is induced by signalling from non-neural niche cells.Cell Physiol Biochem 2006; 18(4-5):275-86
  • 2[1]Lee MK,Cleveland DW.Neuronal intermediate filaments.Annu Rev Neurosci 1996;19:187-217
  • 3[2]Grenier C,Bissonnette C,Volkov L,et al.Molecular morphology and toxicity of cytoplasmic prion protein aggregates in neuronal and non-neuronal cells.J Neurochem 2006;97(5):1456-66
  • 4[3]Chien CL,Liu TC,Ho CL,et al.Overexpression of neuronal intermediate filament protein alpha-intemexin in PC12 cells.J Neurosci Res 2005;80(5):693-706
  • 5[4]Zuwala K,Merigo F,Zancanaro C.Neuronal intermediate filaments in the developing tongue of the frog Rana esculenta.Eur J Histochem 2004;48(2):121-8
  • 6[5]Gervasi C,Thyagarajan A,Szaro BG.Increased expression of multiple neurofilament mRNAs during regeneration of vertebrate central nervous system axons.J Comp Neurol 2003;461 (2):262-75
  • 7[6]Dautingy A,Pham-Dihn D,Roussel C,et al,The large neurofilament subunit (NF-H) of the rat:cDNA cloning and in situ detection.Biochem Biophys Res Commun 1988; 154(3):1099-106
  • 8[8]Tomita M,Mori T,Maruyama K,et al.A comparison of neural differentiation and retinal transplantation with bone marrow-derived cells and retinal progenitor cells.Stem Cells 2006;24(10):2270-8
  • 9[9]Lin H,Schlaepfer WW.Role of neurofilament aggregation in motor neuron disease.Ann Neurol 2006;60(4):399-406
  • 10[10]Aydin MD,Akyol-Salman I,Sahin O.Histopathological changes in ciliary ganglion of rabbits with subarachnoid hemorrhage.Int J Neurosci 2005;115(11):1595-602

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