中华物理医学与康复杂志
中華物理醫學與康複雜誌
중화물리의학여강복잡지
CHINESE JOURNAL OF PHYSICAL MEDICINE AND REHABILITATION
2001年
1期
20-22
,共3页
舒彬%郝林林%袁纯%唐其敏%黄显凯%沈岳%吴宗耀
舒彬%郝林林%袁純%唐其敏%黃顯凱%瀋嶽%吳宗耀
서빈%학림림%원순%당기민%황현개%침악%오종요
激光%成纤维细胞%瘢痕%胶原
激光%成纖維細胞%瘢痕%膠原
격광%성섬유세포%반흔%효원
目的 探讨脉冲掺钕钇铝石榴石(Nd:YAG)激光对体外培养瘢痕成纤维细胞胶原合成的选择性抑制作用。方法 以不同能量密度(500 J/cm2、1 000 J/cm2、1 500 J/cm2和2 000 J/cm2)Nd:YAG激光(波长1 064 nm,脉宽150 μs)照射体外培养增生性瘢痕和正常皮肤成纤维细胞,照射后24 h分别用3H-脯氨酸掺入法和斑点杂交法检测成纤维细胞胶原合成和I型前胶原基因表达。 结果 体外培养增生性瘢痕成纤维细胞胶原合成高于正常皮肤,约为正常皮肤的2倍,I型前胶原基因表达亦明显高于正常皮肤,约为正常皮肤的3倍;以500 J/cm2激光照射,增生性瘢痕与正常皮肤成纤维细胞胶原合成、I型前胶原mRNA水平均无变化,以1 500 J/cm2、2 000 J/cm2能量密度激光照射,增生性瘢痕成纤维细胞胶原合成、I型前胶原mRNA水平都显著降低(P<0.001,P<0.001);正常皮肤成纤维细胞胶原合成、I型前胶原mRNA水平在1 500 J/cm2激光照射后降低(P<0.001,P<0.01),2 000 J/cm2照射后亦显著降低(P<0.001,P<0.05);以1 000 J/cm2照射,增生性瘢痕成纤维细胞胶原合成与I型前胶原基因表达显著下降(P<0.001),而正常皮肤成纤维细胞胶原合成和I型前胶原基因表达却无明显变化。结论 1 000 J/cm2脉冲Nd:YAG激光照射能选择性抑制增生性瘢痕成纤维细胞胶原合成和I型前胶原基因表达。
目的 探討脈遲摻釹釔鋁石榴石(Nd:YAG)激光對體外培養瘢痕成纖維細胞膠原閤成的選擇性抑製作用。方法 以不同能量密度(500 J/cm2、1 000 J/cm2、1 500 J/cm2和2 000 J/cm2)Nd:YAG激光(波長1 064 nm,脈寬150 μs)照射體外培養增生性瘢痕和正常皮膚成纖維細胞,照射後24 h分彆用3H-脯氨痠摻入法和斑點雜交法檢測成纖維細胞膠原閤成和I型前膠原基因錶達。 結果 體外培養增生性瘢痕成纖維細胞膠原閤成高于正常皮膚,約為正常皮膚的2倍,I型前膠原基因錶達亦明顯高于正常皮膚,約為正常皮膚的3倍;以500 J/cm2激光照射,增生性瘢痕與正常皮膚成纖維細胞膠原閤成、I型前膠原mRNA水平均無變化,以1 500 J/cm2、2 000 J/cm2能量密度激光照射,增生性瘢痕成纖維細胞膠原閤成、I型前膠原mRNA水平都顯著降低(P<0.001,P<0.001);正常皮膚成纖維細胞膠原閤成、I型前膠原mRNA水平在1 500 J/cm2激光照射後降低(P<0.001,P<0.01),2 000 J/cm2照射後亦顯著降低(P<0.001,P<0.05);以1 000 J/cm2照射,增生性瘢痕成纖維細胞膠原閤成與I型前膠原基因錶達顯著下降(P<0.001),而正常皮膚成纖維細胞膠原閤成和I型前膠原基因錶達卻無明顯變化。結論 1 000 J/cm2脈遲Nd:YAG激光照射能選擇性抑製增生性瘢痕成纖維細胞膠原閤成和I型前膠原基因錶達。
목적 탐토맥충참녀을려석류석(Nd:YAG)격광대체외배양반흔성섬유세포효원합성적선택성억제작용。방법 이불동능량밀도(500 J/cm2、1 000 J/cm2、1 500 J/cm2화2 000 J/cm2)Nd:YAG격광(파장1 064 nm,맥관150 μs)조사체외배양증생성반흔화정상피부성섬유세포,조사후24 h분별용3H-포안산참입법화반점잡교법검측성섬유세포효원합성화I형전효원기인표체。 결과 체외배양증생성반흔성섬유세포효원합성고우정상피부,약위정상피부적2배,I형전효원기인표체역명현고우정상피부,약위정상피부적3배;이500 J/cm2격광조사,증생성반흔여정상피부성섬유세포효원합성、I형전효원mRNA수평균무변화,이1 500 J/cm2、2 000 J/cm2능량밀도격광조사,증생성반흔성섬유세포효원합성、I형전효원mRNA수평도현저강저(P<0.001,P<0.001);정상피부성섬유세포효원합성、I형전효원mRNA수평재1 500 J/cm2격광조사후강저(P<0.001,P<0.01),2 000 J/cm2조사후역현저강저(P<0.001,P<0.05);이1 000 J/cm2조사,증생성반흔성섬유세포효원합성여I형전효원기인표체현저하강(P<0.001),이정상피부성섬유세포효원합성화I형전효원기인표체각무명현변화。결론 1 000 J/cm2맥충Nd:YAG격광조사능선택성억제증생성반흔성섬유세포효원합성화I형전효원기인표체。
Objective In order to explore the selectively inhibitory effects of pulsed Nd:YAG laser irradiation on collagen production of scar fibroblasts in vitro. Methods Cultured fibroblasts derived from hypertrophic scars (HS) and normal human skin were irradiated with a pulsed Nd:YAG laser(wavelength 1 064 nm, pulse width 150(μs) at various energy density levels (500 J/cm2, 1 000 J/cm2, 1 500 J/cm2 and 2 000 J/cm2). At 24 hours after laser irradiation, collagen production of fibroblasts was measured by the incorporation of [3H]proline. The expression of proα1(I) procollagen mRNA was investigated by blot hybridization techniques. Results Collagen production of HS fibroblasts was significantly increased, as 2 times as that of normal skin fibroblasts. Type I procollagen mRNA level in HS fibroblasts was markedly elevated, as 3 times as that in normal skin fibroblasts. Collagen synthesis and type I procollagen mRNA level in HS fibroblasts remained unchanged at energy level of 500 J/cm2, and were significantly decreased at energy density of 1 500 and 2 000 J/cm2 (P<0.001,P<0.001). Collagen synthesis and type I procollagen mRNA level in normal dermal fibroblasts were markedly decreased at energy density of 1 500 J/cm2 (P<0.001,P<0.05), and were also reduced at energy denstity of 2 000 J/cm2 (P<0.001,P<0.01). Collagen production and type I procollagen mRNA level in HS fibroblasts was markedly reduced at energy density of 1 000 J/cm2 (P<0.001), the dose at which did not affect collagen synthesis and type I procollagen mRNA level in normal dermal fibroblasts. Conclusion Pulsed Nd: YAG laser at energy density of 1 000 J/cm2 can selectively suppress collagen synthesis and type I procollagen mRNA level of HS fibroblasts.