Apostolidou Eleni, Tsilioni Irini, Hatzoglou Chrissi, Molyvdas Paschalis-Adam, Gourgoulianis Konstantinos I
Department of Physiology, University of Thessaly Medical School, Larissa, Biopolis, 41110, Greece.
Open Respir Med J. 2011;5:70-2. doi: 10.2174/1874306401105010070. Epub 2011 Oct 18.
The aim of this study was to evaluate the physicochemical properties of the pleural mesothelial barrier and of the biological markers that facilitate or eliminate the passage of molecules through the pleura.
Pleural fluid samples from sixty-five patients with heart failure were analyzed. The biological markers studied were lactate dehydrogenase (LDH), adenosine deaminase (ADA), interleukin-6 (IL-6), C-reactive protein (CRP), tumor necrosis factor-α (TNF-α), carcinoembryonic antigen (CEA), copper/zinc superoxide dismutase (CuZnSOD), matrix metalloproteinase-2 (MMP-2), -3 (MMP-3), -7(MMP-7), -8 (MMP-8) and -9 (MMP-9). Based on the pleural fluid/serum ratio, these molecules were divided into three groups: a) the LDH-like group with a pleural fluid/serum ratio between 0,4 and 0,8 (LDH, CEA, CuZnSOD, ADA, CRP, MMP-8), b) molecules with a pleural fluid/serum ratio less than 0,4 (MMP-7 and MMP-9) and c) molecules with a pleural fluid/serum ratio equal or above 1 (TNF-α, IL-6, MMP-2 and MMP-3).
No correlation between the molecular radius and the pleural fluid to serum ratio of the above biological markers was found.
The molecular size is not a major determinant for the passage of molecules through the mesothelial barrier. Several other factors may influence the transport of the above molecules to pleural cavity, such as their charge and shape.
本研究旨在评估胸膜间皮屏障的物理化学特性以及促进或消除分子通过胸膜的生物标志物。
分析了65例心力衰竭患者的胸水样本。所研究的生物标志物包括乳酸脱氢酶(LDH)、腺苷脱氨酶(ADA)、白细胞介素-6(IL-6)、C反应蛋白(CRP)、肿瘤坏死因子-α(TNF-α)、癌胚抗原(CEA)、铜/锌超氧化物歧化酶(CuZnSOD)、基质金属蛋白酶-2(MMP-2)、-3(MMP-3)、-7(MMP-7)、-8(MMP-8)和-9(MMP-9)。根据胸水/血清比值,这些分子被分为三组:a)胸水/血清比值在0.4至0.8之间的LDH样组(LDH、CEA、CuZnSOD、ADA、CRP、MMP-8),b)胸水/血清比值小于0.4的分子(MMP-7和MMP-9),c)胸水/血清比值等于或高于1的分子(TNF-α、IL-6、MMP-2和MMP-3)。
未发现上述生物标志物的分子半径与胸水/血清比值之间存在相关性。
分子大小不是分子通过间皮屏障的主要决定因素。其他几个因素可能会影响上述分子向胸腔的转运,例如它们的电荷和形状。