Gene expression profile of lymphatic endothelial cells

被引:7
作者
Wang, Peiliang [2 ]
Cheng, Yongbo [1 ]
机构
[1] 309th Hosp Chinese Peoples Liberat Army, Dept Med Records, Beijing 100091, Peoples R China
[2] Xinjiang Med Univ, Ctr Oncol, Affiliated Hosp 1, Urumqi 830011, Peoples R China
关键词
biological function; expression file; lymphatic endothelial cell; ultrastructure; ADENOVIRUS-RECEPTOR CAR; SMOOTH-MUSCLE-CELLS; ADHESION MOLECULES; GROWTH-FACTOR; PLASMINOGEN-ACTIVATOR; NODE METASTASIS; VEGF-C; LYMPHANGIOGENESIS; VESSELS; BLOOD;
D O I
10.1042/CBI20100871
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The lymphatic system was first described at around the same time as the blood circulation centuries ago, but the biological function elucidation of LECs (lymphatic endothelial cells) is far less than that of BVECs (blood vascular endothelial cells). Since the discovery of molecular markers for LECs and exploration of lymphatic role in tumour metastasis, more attention has been given to basic lymphatic research. Approx. 150 known genes were found to be expressed at the mRNA and protein levels by LECs. These molecules play an important role in lymphangiogenesis, signalling, tumour metastasis, immune function and fluid transport. This review provides a brief outline of gene expression profile of LECs and the molecular biological function, which will give the reader a better understanding about the mechanics of lymphatic function and some pathologies related to the lymphatic system such as lymphoedema, and facilitate advanced scientific research into lymphatic biology.
引用
收藏
页码:1177 / 1187
页数:11
相关论文
共 120 条
[31]  
Hub E, 1998, AM J PATHOL, V152, P749
[32]   TGFβ-induced protein mediates lymphatic endothelial cell adhesion to the extracellular matrix under low oxygen conditions [J].
Irigoyen, M. ;
Anso, E. ;
Salvo, E. ;
Herrerias, J. Dotor de las ;
Martinez-Irujo, J. J. ;
Rouzauta, A. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2008, 65 (14) :2244-2255
[33]   Hypoxia alters the adhesive properties of lymphatic endothelial cells.: A transcriptional and functional study [J].
Irigoyen, M. ;
Anso, E. ;
Martinez, E. ;
Garayoa, M. ;
Martinez-Irujo, J. J. ;
Rouzaut, A. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2007, 1773 (06) :880-890
[34]  
Irjala H, 2003, CANCER RES, V63, P4671
[35]   Significance of pathological evaluation for lymphatic vessel invasion in invasive breast cancer. [J].
Ito M. ;
Moriya T. ;
Ishida T. ;
Usami S. ;
Kasajima A. ;
Sasano H. ;
Ohuchi N. .
Breast Cancer, 2007, 14 (4) :381-387
[36]   LYVE-1, the lymphatic system and tumor lymphangiogenesis [J].
Jackson, DG ;
Prevo, R ;
Clasper, S ;
Banerji, S .
TRENDS IN IMMUNOLOGY, 2001, 22 (06) :317-321
[37]   The lymphatics revisited - New perspectives from the hyaluronan receptor LYVE-1 [J].
Jackson, DG .
TRENDS IN CARDIOVASCULAR MEDICINE, 2003, 13 (01) :1-7
[38]   Lymphatic network and lymphangiogenesis in the gastric wall [J].
Ji, RC ;
Kato, S .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2003, 51 (03) :331-338
[39]   Lymphatic vascular endothelial hyaluronan receptor (LYVE)-1- and CCL21-positive lymphatic compartments in the diabetic thymus [J].
Ji, Rui-Cheng ;
Kurihara, Kazushige ;
Kato, Seiji .
ANATOMICAL SCIENCE INTERNATIONAL, 2006, 81 (04) :201-209
[40]   Multiple expressions of lymphatic markers and morphological evolution of newly formed lymphatics in lymphangioma and lymph node lymphangiogenesis [J].
Ji, Rui-Cheng ;
Eshita, Yuki ;
Xing, Lianping ;
Miura, Masahiro .
MICROVASCULAR RESEARCH, 2010, 80 (02) :195-201