Secretome of Human Endothelial Cells under Shear Stress

被引:36
|
作者
Burghoff, Sandra [1 ]
Schrader, Juergen [1 ]
机构
[1] Univ Dusseldorf, Inst Cardiovasc Physiol, D-40225 Dusseldorf, Germany
关键词
endothelial cells; shear stress; LC-MS/MS; secretome; laminar flow; oscillatory flow; HUMAN VASCULAR ENDOTHELIUM; FREE-FLOW ELECTROPHORESIS; MESSENGER-RNA LEVELS; SMOOTH-MUSCLE-CELLS; GROWTH-FACTOR-I; PROTEOMIC ANALYSIS; SUPEROXIDE-DISMUTASE; BIOMARKER DISCOVERY; FLUID SHEAR; IDENTIFICATION;
D O I
10.1021/pr100937a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Endothelial cells are exposed to different types of shear stress which triggers the secretion of subsets of proteins. In this study, we analyzed the secretome of endothelial cells under static, laminar, and oscillatory flow. To differentiate between endogenously expressed and added proteins, isolated human umbilical vein endothelial cells were labeled with L-Lysine-(13) C-6,N-15(2) and L-Arginine-C-13(6),N-15(4). Shear stress was applied for 24 h using a cone-and-plate viscometer. Proteins from the supernatants were isolated, trypsinized, and finally analyzed using LC-MS/MS (LTQ). Under static control condition 395 proteins could be identified, of which 78 proteins were assigned to the secretome according to Swiss-Prot database. Under laminar shear stress conditions, 327 proteins (83 secreted) and under oscillatory shear stress 507 proteins (79 secreted) were measured. We were able to identify 6 proteins specific for control conditions, 8 proteins specific for laminar shear stress, and 5 proteins specific for oscillatory shear stress. In addition, we identified flow-specific secretion patterns like the increased secretion of cell adhesion proteins and of proteins involved in protein binding. In conclusion, the identification of shear stress specific secreted proteins (101 under different flow conditions) emphasizes the role of endothelial cells in modulating the plasma composition according to the physiological requirements.
引用
收藏
页码:1160 / 1169
页数:10
相关论文
共 50 条
  • [1] Shear Stress Modulates the Secretome of Human Endothelial Cells
    Burghoff, Sandra
    Schrader, Juergen
    CIRCULATION, 2010, 122 (21)
  • [2] Primary cilia of human endothelial cells disassemble under laminar shear stress
    Iomini, C
    Tejada, K
    Mo, WJ
    Vaananen, H
    Piperno, G
    JOURNAL OF CELL BIOLOGY, 2004, 164 (06): : 811 - 817
  • [3] STRESS FIBERS (SF) IN HUMAN-ENDOTHELIAL CELLS (HEC) UNDER SHEAR-STRESS
    FRANKE, RP
    GRAFE, M
    DAUER, U
    SCHNITTLER, H
    MITTERMAYER, C
    KLINISCHE WOCHENSCHRIFT, 1986, 64 (19): : 989 - 992
  • [4] Induction of fractalkine by endothelial cells under shear stress
    Moatti, D
    Vele, O
    Nemerson, Y
    BLOOD COAGULATION & FIBRINOLYSIS, 2004, 15 (02) : 197 - 197
  • [5] Shear stress inhibits apoptosis of human endothelial cells
    Dimmeler, S
    Haendeler, J
    Rippmann, V
    Nehls, M
    Zeiher, AM
    FEBS LETTERS, 1996, 399 (1-2) : 71 - 74
  • [6] Shear stress prevents apoptosis of human endothelial cells
    Dimmeler, S
    Haendeler, J
    Neuls, M
    Zeiher, AM
    CIRCULATION, 1996, 94 (08) : 2757 - 2757
  • [7] Glycoproteomic Analysis of the Secretome of Human Endothelial Cells
    Yin, Xiaoke
    Bern, Marshall
    Xing, Qiuru
    Ho, Jenny
    Viner, Rosa
    Mayr, Manuel
    MOLECULAR & CELLULAR PROTEOMICS, 2013, 12 (04) : 956 - 978
  • [8] Regulation of the endothelin system by ''shear stress'' in human endothelial cells
    Morawietz, H
    Schubert, A
    Schluter, J
    Szibor, M
    Ruckschloss, U
    Darmer, D
    Holtz, J
    PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1997, 433 (06): : O44 - O44
  • [9] Regulation of the endothelin system by shear stress in human endothelial cells
    Morawietz, H
    Talanow, R
    Szibor, M
    Rueckschloss, U
    Schubert, A
    Bartling, B
    Darmer, D
    Holtz, J
    JOURNAL OF PHYSIOLOGY-LONDON, 2000, 525 (03): : 761 - 770
  • [10] Regulation of Nox isoforms by shear stress in human endothelial cells
    Duerrschmidt, N
    Stielow, C
    Müller, G
    Morawietz, H
    JOURNAL OF VASCULAR RESEARCH, 2005, 42 : 57 - 57