M. S. Sacks, L. Bowes, E. D. Hiester, J. Brahmatewari, P. Mertz, W. Eaglstein
{"title":"小角光散射用于真皮创面胶原蛋白结构分析","authors":"M. S. Sacks, L. Bowes, E. D. Hiester, J. Brahmatewari, P. Mertz, W. Eaglstein","doi":"10.1109/SBEC.1998.666678","DOIUrl":null,"url":null,"abstract":"MTRODUCTION. The process of demal wound heaiing is a very complex one, taking place in several consecutive stages. Cytokines, in particular growth factors, are important in rhe regulation of these stages. Transforming Growth Factor p (TGFP) is known to play a crucial role during inflammation and extracellular ma^ deposition. Chronic exposure to large amounts of TGFP may promote excessive fibrosis. Attempts to prevent fibrosis and scarring have been aimed at lowering the levels of TGFP in the wound site. Local application of neutralizing antibodies to TGFP (Ab-TGFP) has been shown to signpiticantly decrease the amount of scarring during wound h e a h g . Small angle light scattering (SALS) offers a means to quantitatively determine differences in collagen fiber orientation and directional uniformity during the would healing process in the presence of TGFP or Ab-TGFP. In this study, we demonstrate that SALS can be used to quantify differences in the collagen fiber architecture of histological sections taken from dermal wounds that exposed to TGFP and Ab-TGFP. METHODS. Recombinant human TGFP2 and Ab-TGFP;, of the IgG subtype were utilized with a methylcellulose 2% gel as the delivery vehicle. Two white specific pathogen pigs (15-20Kg) were wounded according to established procedures following AAALAC standards. Biopsies were performed on days 7, 14, and 46 post-wounding, with normal unwounded s!un also taken as the conuol. Tissue specimens were fixed and standard histological sections prepared using H&E staining. A detailed description of the SALS device and its accuracy in tissue structural analysis has been previously presented (Sacks, et al. 1997). Briefly, a 4 mW HeNe (X = 632.8 nm) continuous unpolarized wave laser is passed Wough the tlssue specimen, which scatters light according to the internal fiber structure within the light beam envelope (Fig. 1). The information obtainable from thc scattered light distribution I (0) includes the preferred fiber . drrection, defined as the cennoid of I(O), and the degree of orientation defined as the angle containmg half of the total area under the I(cD), representing 50% of the fibers (Sacks, et al. 1997). After SALS scanning, the data was analyzed and the degree of orientation and collagen preferred directions mapped (Fig. 2). SALS data from the wounded section was extracted and the means for degree of orientation computed. RESULTS A N D DISCUSSION. Normal skin revealed the lowest degree of orientation (54.6\"), while the TGFP treated wounds had a significantly greater (p < 0.0001) degree of orientation at days 7 and 14. The greater degree of orientation is consistent the presence of fibrosis in the wound site. Specimens treated with Ab-TGFPL3 displayed a degree of orientation intermediate between normal and TGFP treated wounds. By day 46, wound architectures were indistinguishable. These results suggest that SALS can be used to detect a d quanti@ the differences in collagen fiber onentation in normal ealing skin wounds. t Scattering I","PeriodicalId":122159,"journal":{"name":"Proceedings of the 17th Southern Biomedical Engineering Conference","volume":"73 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1998-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Small Angle Light Scattering for Dermal Wound Collagen Structural Analysis\",\"authors\":\"M. S. Sacks, L. Bowes, E. D. Hiester, J. Brahmatewari, P. Mertz, W. Eaglstein\",\"doi\":\"10.1109/SBEC.1998.666678\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"MTRODUCTION. The process of demal wound heaiing is a very complex one, taking place in several consecutive stages. Cytokines, in particular growth factors, are important in rhe regulation of these stages. Transforming Growth Factor p (TGFP) is known to play a crucial role during inflammation and extracellular ma^ deposition. Chronic exposure to large amounts of TGFP may promote excessive fibrosis. Attempts to prevent fibrosis and scarring have been aimed at lowering the levels of TGFP in the wound site. Local application of neutralizing antibodies to TGFP (Ab-TGFP) has been shown to signpiticantly decrease the amount of scarring during wound h e a h g . Small angle light scattering (SALS) offers a means to quantitatively determine differences in collagen fiber orientation and directional uniformity during the would healing process in the presence of TGFP or Ab-TGFP. In this study, we demonstrate that SALS can be used to quantify differences in the collagen fiber architecture of histological sections taken from dermal wounds that exposed to TGFP and Ab-TGFP. METHODS. Recombinant human TGFP2 and Ab-TGFP;, of the IgG subtype were utilized with a methylcellulose 2% gel as the delivery vehicle. Two white specific pathogen pigs (15-20Kg) were wounded according to established procedures following AAALAC standards. Biopsies were performed on days 7, 14, and 46 post-wounding, with normal unwounded s!un also taken as the conuol. Tissue specimens were fixed and standard histological sections prepared using H&E staining. A detailed description of the SALS device and its accuracy in tissue structural analysis has been previously presented (Sacks, et al. 1997). Briefly, a 4 mW HeNe (X = 632.8 nm) continuous unpolarized wave laser is passed Wough the tlssue specimen, which scatters light according to the internal fiber structure within the light beam envelope (Fig. 1). The information obtainable from thc scattered light distribution I (0) includes the preferred fiber . drrection, defined as the cennoid of I(O), and the degree of orientation defined as the angle containmg half of the total area under the I(cD), representing 50% of the fibers (Sacks, et al. 1997). After SALS scanning, the data was analyzed and the degree of orientation and collagen preferred directions mapped (Fig. 2). SALS data from the wounded section was extracted and the means for degree of orientation computed. RESULTS A N D DISCUSSION. Normal skin revealed the lowest degree of orientation (54.6\\\"), while the TGFP treated wounds had a significantly greater (p < 0.0001) degree of orientation at days 7 and 14. The greater degree of orientation is consistent the presence of fibrosis in the wound site. Specimens treated with Ab-TGFPL3 displayed a degree of orientation intermediate between normal and TGFP treated wounds. By day 46, wound architectures were indistinguishable. 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引用次数: 1
摘要
MTRODUCTION。创伤愈合是一个非常复杂的过程,分几个连续的阶段进行。细胞因子,特别是生长因子,在这些阶段的调节中很重要。已知转化生长因子p (TGFP)在炎症和细胞外沉积中起关键作用。长期暴露于大量TGFP可促进过度纤维化。预防纤维化和瘢痕形成的尝试旨在降低伤口部位的TGFP水平。局部应用TGFP中和抗体(Ab-TGFP)已被证明可以显著减少伤口愈合期间的疤痕数量。小角度光散射(SALS)提供了一种定量测定在TGFP或Ab-TGFP存在下胶原纤维在愈合过程中取向和方向均匀性差异的方法。在这项研究中,我们证明了SALS可以用来量化暴露于TGFP和Ab-TGFP的真皮伤口的组织学切片的胶原纤维结构差异。方法。IgG亚型的重组人TGFP2和Ab-TGFP,用2%甲基纤维素凝胶作为递送载体。按照AAALAC标准建立的程序伤伤2头白色特异性病原体猪(15-20Kg)。伤后第7天、第14天、第46天行活组织检查,正常未伤5例。联合国也采取了控制措施。组织标本固定,H&E染色制备标准组织学切片。SALS设备的详细描述及其在组织结构分析中的准确性之前已经提出过(Sacks, et al. 1997)。简单地说,通过一个4 mW的HeNe (X = 632.8 nm)连续无偏振波激光穿过组织试样,该激光根据光束包络内的光纤内部结构对光进行散射(图1)。从散射光分布I(0)中可以得到的信息包括首选光纤。方向,定义为I(O)的质心,取向度定义为包含I(cD)下总面积的一半的角度,代表50%的纤维(Sacks, et al. 1997)。经SALS扫描后,对数据进行分析,绘制出取向度和胶原偏好方向图(图2)。提取损伤切片的SALS数据,计算取向度均值。结果并进行了讨论。正常皮肤显示最低的取向度(54.6”),而TGFP处理的伤口在第7天和第14天的取向度显著增加(p < 0.0001)。更大程度的定向与伤口部位纤维化的存在一致。用Ab-TGFPL3处理的标本显示出介于正常和TGFP处理的伤口之间的定向程度。到第46天,伤口结构已无法区分。这些结果表明,SALS可用于定量检测正常愈合皮肤伤口中胶原纤维含量的差异。散射I
Small Angle Light Scattering for Dermal Wound Collagen Structural Analysis
MTRODUCTION. The process of demal wound heaiing is a very complex one, taking place in several consecutive stages. Cytokines, in particular growth factors, are important in rhe regulation of these stages. Transforming Growth Factor p (TGFP) is known to play a crucial role during inflammation and extracellular ma^ deposition. Chronic exposure to large amounts of TGFP may promote excessive fibrosis. Attempts to prevent fibrosis and scarring have been aimed at lowering the levels of TGFP in the wound site. Local application of neutralizing antibodies to TGFP (Ab-TGFP) has been shown to signpiticantly decrease the amount of scarring during wound h e a h g . Small angle light scattering (SALS) offers a means to quantitatively determine differences in collagen fiber orientation and directional uniformity during the would healing process in the presence of TGFP or Ab-TGFP. In this study, we demonstrate that SALS can be used to quantify differences in the collagen fiber architecture of histological sections taken from dermal wounds that exposed to TGFP and Ab-TGFP. METHODS. Recombinant human TGFP2 and Ab-TGFP;, of the IgG subtype were utilized with a methylcellulose 2% gel as the delivery vehicle. Two white specific pathogen pigs (15-20Kg) were wounded according to established procedures following AAALAC standards. Biopsies were performed on days 7, 14, and 46 post-wounding, with normal unwounded s!un also taken as the conuol. Tissue specimens were fixed and standard histological sections prepared using H&E staining. A detailed description of the SALS device and its accuracy in tissue structural analysis has been previously presented (Sacks, et al. 1997). Briefly, a 4 mW HeNe (X = 632.8 nm) continuous unpolarized wave laser is passed Wough the tlssue specimen, which scatters light according to the internal fiber structure within the light beam envelope (Fig. 1). The information obtainable from thc scattered light distribution I (0) includes the preferred fiber . drrection, defined as the cennoid of I(O), and the degree of orientation defined as the angle containmg half of the total area under the I(cD), representing 50% of the fibers (Sacks, et al. 1997). After SALS scanning, the data was analyzed and the degree of orientation and collagen preferred directions mapped (Fig. 2). SALS data from the wounded section was extracted and the means for degree of orientation computed. RESULTS A N D DISCUSSION. Normal skin revealed the lowest degree of orientation (54.6"), while the TGFP treated wounds had a significantly greater (p < 0.0001) degree of orientation at days 7 and 14. The greater degree of orientation is consistent the presence of fibrosis in the wound site. Specimens treated with Ab-TGFPL3 displayed a degree of orientation intermediate between normal and TGFP treated wounds. By day 46, wound architectures were indistinguishable. These results suggest that SALS can be used to detect a d quanti@ the differences in collagen fiber onentation in normal ealing skin wounds. t Scattering I