Pfister R R, Haddox J L, Sommers C I
The Eye Research Laboratories, Brookwood Medical Center, Birmingham, Alabama, USA.
Invest Ophthalmol Vis Sci. 1998 Aug;39(9):1744-50.
The objective of this study was to establish and characterize the invasion of polymorphonuclear leukocytes (PMNs) into a normal cornea after intrastromal injection of the tripeptide chemoattractants generated from alkali-degraded corneas.
The following samples were injected into the midstroma of normal rabbit corneas: ultrafiltered tripeptide chemoattractants (N-acetyl-proline-glycine-proline and N-methyl-proline-glycine-proline) generated from alkali-degraded corneas, synthetic N-acetyl-PGP, positive control (leukotriene B4 [LTB4]), or negative control (Hanks' balanced salt solution [HBSS]). Timed responses of PMN infiltration were established for effective concentrations of LTB4 or the ultrafiltered chemoattractants.
All intrastromal injections resulted in the immediate development of an edematous disc that was 10 mm in diameter. The lesion essentially had cleared in the HBSS-injected eyes by 8 hours, and histologic sections revealed minimal numbers of PMNs in the cornea or limbal tissue. The injection of LTB4 or the ultrafiltered tripeptide chemoattractants induced peak numbers of PMNs within the stroma at 8 hours, subsiding by 16 hours. Seventy units of ultrafiltered chemoattractants yielded a strong PMN response, similar to 1 X 10(-5) M LTB4. The highest concentration of ultrafiltered chemoattractants (350 U) produced a severe PMN response that was characterized by a solid sheet of neutrophils surrounding the injection site. The injection of synthetic N-acetyl-PGP (2 X 10(-4) M) produced a marked PMN response.
PMN invasion of the normal cornea after the injection of the ultrafiltered tripeptide chemoattractants or the synthetic N-acetyl-PGP mimicked early PMN infiltration in the alkali-injured eye, confirming the importance of this chemoattractant as an inflammatory mediator.
本研究的目的是在基质内注射由碱降解角膜产生的三肽趋化因子后,建立并描述多形核白细胞(PMN)侵入正常角膜的情况。
将以下样本注射到正常兔角膜基质中部:由碱降解角膜产生的超滤三肽趋化因子(N - 乙酰 - 脯氨酸 - 甘氨酸 - 脯氨酸和N - 甲基 - 脯氨酸 - 甘氨酸 - 脯氨酸)、合成的N - 乙酰 - PGP、阳性对照(白三烯B4 [LTB4])或阴性对照(汉克斯平衡盐溶液[HBSS])。针对LTB4或超滤趋化因子的有效浓度确定PMN浸润的定时反应。
所有基质内注射均导致立即出现直径为10 mm的水肿盘。在注射HBSS的眼中,病变在8小时基本消退,组织学切片显示角膜或角膜缘组织中的PMN数量极少。注射LTB4或超滤三肽趋化因子在8小时时诱导基质内PMN数量达到峰值,16小时时减少。70单位的超滤趋化因子产生强烈的PMN反应,类似于1×10⁻⁵ M LTB4。超滤趋化因子的最高浓度(350 U)产生严重的PMN反应,其特征是注射部位周围有一层密集的中性粒细胞。注射合成的N - 乙酰 - PGP(2×10⁻⁴ M)产生明显的PMN反应。
注射超滤三肽趋化因子或合成的N - 乙酰 - PGP后,PMN侵入正常角膜模拟了碱损伤眼中早期PMN浸润,证实了这种趋化因子作为炎症介质的重要性。