The Cerebral Surfactant System and Its Alteration in Hydrocephalic Conditions

被引:64
作者
Schob, Stefan [1 ]
Lobsien, Donald [1 ]
Friedrich, Benjamin [3 ]
Bernhard, Matthias K. [4 ]
Gebauer, Corinna [5 ]
Dieckow, Julia [6 ]
Gawlitza, Matthias [1 ]
Pirlich, Mandy [7 ]
Saur, Dorothee [7 ]
Braeuer, Lars [9 ]
Bechmann, Ingo [8 ]
Hoffmann, Karl-Titus [1 ]
Mahr, Cynthia V. [2 ]
Nestler, Ulf [2 ]
Preuss, Matthias [2 ]
机构
[1] Univ Leipzig, Dept Neuroradiol, D-04109 Leipzig, Germany
[2] Univ Leipzig, Dept Neurosurg, D-04109 Leipzig, Germany
[3] Univ Leipzig, Dept Diagnost & Intervent Radiol, D-04109 Leipzig, Germany
[4] Univ Leipzig, Div Neuropediat, D-04109 Leipzig, Germany
[5] Univ Leipzig, Dept Neonatol, D-04109 Leipzig, Germany
[6] Univ Leipzig, Dept Ophthalmol, D-04109 Leipzig, Germany
[7] Univ Leipzig, Dept Neurol, D-04109 Leipzig, Germany
[8] Univ Leipzig, Inst Anat, D-04109 Leipzig, Germany
[9] Univ Erlangen Nurnberg, Inst Anat, Erlangen, Germany
关键词
PROTEIN-A; MECHANICAL FORCES; COLLECTINS; RELEASE; INNATE; ROLES; FLUID;
D O I
10.1371/journal.pone.0160680
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction Pulmonary Surfactant reduces surface tension in the terminal airways thus facilitating breathing and contributes to host's innate immunity. Surfactant Proteins (SP) A, B, C and D were recently identified as inherent proteins of the CNS. Aim of the study was to investigate cerebrospinal fluid (CSF) SP levels in hydrocephalus patients compared to normal subjects. Patients and Methods CSF SP A-D levels were quantified using commercially available ELISA kits in 126 patients (0-84 years, mean 39 years). 60 patients without CNS pathologies served as a control group. Hydrocephalus patients were separated in aqueductal stenosis (AQS, n = 24), acute hydrocephalus without aqueductal stenosis (acute HC w/o AQS, n = 16) and idiopathic normal pressure hydrocephalus (NPH, n = 20). Furthermore, six patients with pseudotumor cerebri were investigated. Results SP A D D are present under physiological conditions in human CSF. SP-A is elevated in diseases accompanied by ventricular enlargement (AQS, acute HC w/o AQS) in a significant manner (0.67, 1.21 vs 0.38 ng/ml in control, p<0.001). SP-C is also elevated in hydrocephalic conditions (AQS, acute HC w/o AQS; 0.87, 1.71 vs. 0.48 ng/ml in controls, p<0.001) and in Pseudotumor cerebri (1.26 vs. 0.48 ng/ml in controls, p<0.01). SP-B and SP-D did not show significant alterations. Conclusion The present study confirms the presence of SPs in human CSF. There are significant changes of SP-A and SP-C levels in diseases affecting brain water circulation and elevation of intracranial pressure. Cause of the alterations, underlying regulatory mechanisms, as well as diagnostic and therapeutic consequences of cerebral SP's requires further thorough investigations.
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