Regional difference in epidermal thinning after skin denervation

被引:36
作者
Chiang, HY
Huang, IT
Chen, WP
Chien, HF
Shun, CT
Chang, YC
Hsieh, ST
机构
[1] Natl Taiwan Univ, Coll Med, Dept Anat, Taipei 10018, Taiwan
[2] Natl Taiwan Univ, Coll Med, Dept Surg, Taipei 10018, Taiwan
[3] Natl Taiwan Univ, Coll Med, Dept Pathol, Taipei 10018, Taiwan
[4] Natl Taiwan Univ, Coll Med, Dept Neurol, Taipei 10018, Taiwan
关键词
skin innervation; protein gene product 9.5; unmyelinated nerves; axonal degeneration; nerve degeneration; epidermis; keratinocyte;
D O I
10.1006/exnr.1998.6896
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Denervation of skin has a profound influence on epidermis; epidermal thinning was a consistent finding in rats. However, it is not clear whether the degree of epidermal thinning was similar in the region receiving the same innervation. In mice, how early epidermal nerves were degenerated after nerve injury remained unknown. To address these issues, we transected the sciatic nerve in mice and compared the changes of epidermal thickness in different areas of the hind foot skin. Epidermal nerves degenerated within 48 h after nerve transection, similar to what was observed in rats. Seven days after nerve transection, there was differential thinning of epidermis. The interpad area, in the center of the sciatic nerve-innervated region, exhibited the most profound degree of epidermal thinning (34.6 +/- 3.1 vs 47.8 +/- 2.4 mu m, P < 0.01). The heel area, in the periphery of the sciatic nerve-innervated zone, did not show significant thinning of epidermis after denervation (37.3 +/- 4.8 vs 41.5 +/- 5.1 mu m, P > 0.05). The degree of epidermal thinning after denervation in the pad area was the intermediate one: with 98.8 +/- 4.8 vs 120.1 +/- 7.3 mu m, P < 0.02, in the rete pegs, and 51.1 +/- 4.1 vs 62.1 +/- 6.0 mu m, P < 0.02, in the dermal papilla. The differential thinning was obvious when the thickness of the denervated epidermis was normalized to that of the control epidermis with the ratios of 0.73 +/- 0.03 in the interpad area, 0.83 +/- 0.04 in the rete peg, 0.85 +/- 0.05 in the dermal papilla, and 0.92 +/- 0.05 in the heel. Epidermal thinning was reversed by reinnervation of the epidermis after sciatic nerve crush (41.5 +/- 1.5 vs 45.0 +/- 2.0 mu m in the interpad area, P > 0.05). These findings suggest that sensory nerves exhibit trophic influences on the epidermis presumably through the effects of diffusible factors. (C) 1998 Academic Press.
引用
收藏
页码:137 / 145
页数:9
相关论文
共 43 条
[1]   OVEREXPRESSION OF NERVE GROWTH-FACTOR IN EPIDERMIS OF TRANSGENIC MICE CAUSES HYPERTROPHY OF THE PERIPHERAL NERVOUS-SYSTEM [J].
ALBERS, KM ;
WRIGHT, DE ;
DAVIS, BM .
JOURNAL OF NEUROSCIENCE, 1994, 14 (03) :1422-1432
[2]   SUBSTANCE-P AND NITRIC-OXIDE MEDIATE WOUND-HEALING OF ULTRAVIOLET PHOTODAMAGED RAT SKIN - EVIDENCE FOR AN EFFECT OF NITRIC-OXIDE ON KERATINOCYTE PROLIFERATION [J].
BENRATH, J ;
ZIMMERMAN, M ;
GILLARDON, F .
NEUROSCIENCE LETTERS, 1995, 200 (01) :17-20
[3]   Nerve growth factor induces the expression of certain cytokine genes and bcl-2 in mast cells - Potential role in survival promotion [J].
Bullock, ED ;
Johnson, EM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (44) :27500-27508
[4]   ALTERED EXPRESSION OF NERVE GROWTH-FACTOR IN THE SKIN OF TRANSGENIC MICE LEADS TO CHANGES IN RESPONSE TO MECHANICAL STIMULI [J].
DAVIS, BM ;
LEWIN, GR ;
MENDELL, LM ;
JONES, ME ;
ALBERS, KM .
NEUROSCIENCE, 1993, 56 (04) :789-792
[5]   2 MODES OF CUTANEOUS RE-INNERVATION FOLLOWING PERIPHERAL-NERVE INJURY [J].
DEVOR, M ;
SCHONFELD, D ;
SELTZER, Z ;
WALL, PD .
JOURNAL OF COMPARATIVE NEUROLOGY, 1979, 185 (01) :211-220
[6]  
DIMARCO E, 1993, J BIOL CHEM, V268, P22838
[7]   EPIDERMAL DIFFERENTIATION - THE BARE ESSENTIALS [J].
FUCHS, E .
JOURNAL OF CELL BIOLOGY, 1990, 111 (06) :2807-2814
[8]   CHARACTERIZATION OF CHLORIDE AND CATION CHANNELS IN CULTURED HUMAN KERATINOCYTES [J].
GALIETTA, LJV ;
BARONE, V ;
DELUCA, M ;
ROMEO, G .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1991, 418 (1-2) :18-25
[9]   Activation of keratinocyte nicotinic cholinergic receptors stimulates calcium influx and enhances cell differentiation [J].
Grando, SA ;
Horton, RM ;
Mauro, TM ;
Kist, DA ;
Lee, TX ;
Dahl, MV .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (03) :412-418
[10]  
Griffin J.W., 1993, PERIPHERAL NEUROPATH, VThird, P361