Expression of Janus kinase 3 in human endothelial and other non-lymphoid and non-myeloid cells

被引:62
作者
Verbsky, JW
Bach, EA
Fang, YF
Yang, LP
Randolph, DA
Fields, LE
机构
[1] WASHINGTON UNIV, SCH MED, DEPT MED, ST LOUIS, MO 63110 USA
[2] WASHINGTON UNIV, SCH MED, DEPT PATHOL, ST LOUIS, MO 63110 USA
关键词
D O I
10.1074/jbc.271.24.13976
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Members of the Janus kinase (Jak) family of protein tyrosine kinases have recently been implicated in the proximal signal transduction events of cytokine receptors, Jak3, a newly discovered member of this family, is believed to be normally limited in its expression to cells of the lymphoid and myeloid lineages, Herein we show that Jak3 is expressed in primary human vascular cells, as well as other non-lymphoid and non-myeloid cell types. Reverse transcriptase-polymerase chain reaction and Northern blot analysis revealed that Jak3 mRNA was expressed at low levels in human umbilical vein endothelial cells (HUVEC), human aortic smooth muscle cells (HASMC), A549 (human lung carcinoma), and DLD-1 (human colon adenocarcinoma) cells. Higher basal levels of Jak3 mRNA were detected in HMEC-1 (human microvascular cell line) and HepG2 (human hepatocellular carcinoma) cells. Jak3 mRNA expression was induced in HUVEC, HMEC-1, and HASMC by treatment with interleukin-1 beta, tumor necrosis factor-alpha, interferon-gamma, and lipopolysaccharide. Jak3 protein was detectable at low levels in untreated HMEC-1, and these levels increased significantly with cytokine treatment. Furthermore, Jak3 protein was phosphorylated upon treatment of these cells with interleukin-4. This work shows that Jak3 is expressed or inducible in human vascular endothelial, vascular smooth muscle, and other nonlymphoid and non-myeloid cells, suggesting a broader role for Jak3 in the cytokine signal transduction of these cells.
引用
收藏
页码:13976 / 13980
页数:5
相关论文
共 30 条
[1]   NOVEL PROTEIN-KINASES EXPRESSED IN HUMAN BREAST-CANCER [J].
CANCE, WG ;
CRAVEN, RJ ;
WEINER, TM ;
LIU, ET .
INTERNATIONAL JOURNAL OF CANCER, 1993, 54 (04) :571-577
[2]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[3]   ENDOTHELIAL EXPRESSION OF A MONONUCLEAR LEUKOCYTE ADHESION MOLECULE DURING ATHEROGENESIS [J].
CYBULSKY, MI ;
GIMBRONE, MA .
SCIENCE, 1991, 251 (4995) :788-791
[4]   JAK-STAT PATHWAYS AND TRANSCRIPTIONAL ACTIVATION IN RESPONSE TO IFNS AND OTHER EXTRACELLULAR SIGNALING PROTEINS [J].
DARNELL, JE ;
KERR, IM ;
STARK, GR .
SCIENCE, 1994, 264 (5164) :1415-1421
[5]  
FIRMBACHKRAFT I, 1990, ONCOGENE, V5, P1329
[6]   IL-4 AND IL-13 EXHIBIT COMPARABLE ABILITIES TO REDUCE PYROGEN-INDUCED EXPRESSION OF PROCOAGULANT ACTIVITY IN ENDOTHELIAL-CELLS AND MONOCYTES [J].
HERBERT, JM ;
SAVI, P ;
LAPLACE, MC ;
LALE, A ;
DOL, F ;
DUMAS, A ;
LABIT, C ;
MINTY, A .
FEBS LETTERS, 1993, 328 (03) :268-270
[7]   INTERLEUKIN 4 INDUCES INTERLEUKIN 6 PRODUCTION BY ENDOTHELIAL-CELLS - SYNERGY WITH INTERFERON-GAMMA [J].
HOWELLS, G ;
PHAM, P ;
TAYLOR, D ;
FOXWELL, B ;
FELDMANN, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (01) :97-101
[8]   REGULATION OF VASCULAR CELL-ADHESION MOLECULE-1 EXPRESSION BY IL-4 AND TNF-ALPHA IN CULTURED ENDOTHELIAL-CELLS [J].
IADEMARCO, MF ;
BARKS, JL ;
DEAN, DC .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (01) :264-271
[9]   SIGNALING THROUGH THE HEMATOPOIETIC CYTOKINE RECEPTORS [J].
IHLE, JN ;
WITTHUHN, BA ;
QUELLE, FW ;
YAMAMOTO, K ;
SILVENNOINEN, O .
ANNUAL REVIEW OF IMMUNOLOGY, 1995, 13 :369-398
[10]   CYTOKINE RECEPTOR SIGNALING MECHANISMS [J].
KARNITZ, LM ;
ABRAHAM, RT .
CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (03) :320-326