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通过芥子气在体内诱导产生的兔皮肤损伤在器官培养中释放的炎性介质和调节剂。I. 定量组织病理学;中性粒细胞、嗜碱性粒细胞和单核细胞存活情况;以及未结合(血清)蛋白含量。

Inflammatory mediators and modulators released in organ culture from rabbit skin lesions produced in vivo by sulfur mustard. I. Quantitative histopathology; PMN, basophil, and mononuclear cell survival; and unbound (serum) protein content.

作者信息

Dannenberg A M, Pula P J, Liu L H, Harada S, Tanaka F, Vogt R F, Kajiki A, Higuchi K

出版信息

Am J Pathol. 1985 Oct;121(1):15-27.

PMID:4050973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1888029/
Abstract

When applied topically to the skin of rabbits in vivo, sulfur mustard (SM), the vesicant used in World War I, produced a slowly developing inflammatory response, which peaked in size at 1 and 2 days, ulcerated within 3 days, and reepithelialized by 10 days. Histologically, basophils and polymorphonuclear leukocytes (PMNs) were common in both early and late lesions, and the crust over the ulcers was composed of dead epidermal cells, fibrin, and large numbers of PMNs. Healing occurred under the crust by migration of epidermal cells from the margins of the lesions and from the hair follicles. In organ culture, the lesion explants survived well, and reepithelialization even took place. Their excellent survival enabled us to compare the life spans of the infiltrating leukocytes within an inflammatory site. PMNs within the explants began disappearing during the first day of culture, and almost all had disappeared by 3 days. In contrast, over half of the basophils and the mononuclear cells within the explants were still present after 3 days of culture. The 1-, 2-, 3-, 6-, and 10-day (1.0-sq cm) SM lesion biopsies showed a 30-45% increase in weight (when compared with normal skin), presumably due to the extravasation of serum proteins and the fluids retained by them. When the biopsies were organ-cultured for 3 days, the 1-, 2-, and 3-day lesions lost weight, and the 6- and 10-day lesions (and normal skin) gained weight. These weight differences were not due to the amount of unbound protein extractable into the culture fluids, because both the early lesions and the late lesions contained about the same amount of unbound protein. The most likely explanation for these weight differences is that the newly formed ground substances of late lesions absorbed culture fluid, because the ground substance had changed from the sol state of acute inflammation (in which it was extractable) back to its normal gel state (in which it was not extractable). The unbound protein extractable into the culture fluids was mostly of serum origin. This protein averaged 1.9 mg for 1.0 sq cm normal skin explants (with a mean weight of 215 mg), and 6.4 mg for 1-day SM lesions (with a mean weight of 313 mg). Because rabbit serum contains about 60 mg protein/ml, these figures indicate that normal skin contained about 15% (unbound) serum by weight.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

第一次世界大战中使用的糜烂性毒剂芥子气(SM),经局部涂抹于家兔活体皮肤后,引发了缓慢发展的炎症反应,该反应在1至2天时面积达到峰值,3天内出现溃疡,10天时重新上皮化。组织学上,嗜碱性粒细胞和多形核白细胞(PMN)在早期和晚期损伤中均很常见,溃疡表面的痂皮由死亡的表皮细胞、纤维蛋白和大量PMN组成。损伤边缘和毛囊的表皮细胞迁移,使得痂皮下实现愈合。在器官培养中,损伤外植体存活良好,甚至发生了重新上皮化。其良好的存活状况使我们能够比较炎症部位浸润白细胞的寿命。外植体内的PMN在培养的第一天开始消失,到3天时几乎全部消失。相比之下,培养3天后,外植体内超过一半的嗜碱性粒细胞和单核细胞仍然存在。芥子气损伤1、2、3、6和10天(1.0平方厘米)的活检组织显示重量增加30%至45%(与正常皮肤相比),这可能是由于血清蛋白外渗及其潴留的液体所致。当活检组织进行3天器官培养时,1、2和3天损伤的组织重量减轻,6和10天损伤的组织(以及正常皮肤)重量增加。这些重量差异并非由于可提取到培养液中的未结合蛋白量不同,因为早期损伤和晚期损伤所含未结合蛋白量大致相同。这些重量差异最可能的解释是,晚期损伤新形成的基质吸收了培养液,因为基质已从急性炎症的溶胶状态(此时可提取)变回其正常的凝胶状态(此时不可提取)。可提取到培养液中的未结合蛋白大多源自血清。每1.0平方厘米正常皮肤外植体(平均重量215毫克)的这种蛋白平均为1.9毫克,1天芥子气损伤组织(平均重量313毫克)的为6.4毫克。由于兔血清含约60毫克蛋白/毫升,这些数据表明正常皮肤按重量计约含15%(未结合)血清。(摘要截选至400字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/aff57bc66e89/amjpathol00163-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/7919dcb94ba7/amjpathol00163-0026-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/15d496f3b730/amjpathol00163-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/8a7b73cbdb58/amjpathol00163-0027-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/aff57bc66e89/amjpathol00163-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/7919dcb94ba7/amjpathol00163-0026-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/15d496f3b730/amjpathol00163-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/8a7b73cbdb58/amjpathol00163-0027-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c0b/1888029/aff57bc66e89/amjpathol00163-0028-a.jpg

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