ROLE OF SCATTER FACTOR IN THE PATHOGENESIS OF AIDS-RELATED KAPOSI-SARCOMA

被引:91
作者
NAIDU, YM
ROSEN, EM
ZITNICK, R
GOLDBERG, I
PARK, M
NAUJOKAS, M
POLVERINI, PJ
NICKOLOFF, BJ
机构
[1] UNIV MICHIGAN, SCH MED, DEPT PATHOL, ANN ARBOR, MI 48109 USA
[2] YALE UNIV, SCH MED, DEPT THERAPEUT RADIOL, NEW HAVEN, CT 06510 USA
[3] LONG ISL JEWISH MED CTR, DEPT RADIAT ONCOL, NEW HYDE PK, NY 11042 USA
[4] MCGILL UNIV, ROYAL VICTORIA HOSP, MOLEC ONCOL GRP, MONTREAL H3A 1A1, PQ, CANADA
[5] UNIV MICHIGAN, SCH DENT, DEPT ORAL PATHOL, ANN ARBOR, MI 48109 USA
关键词
D O I
10.1073/pnas.91.12.5281
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
Kaposi sarcoma (KS) is a complex multicellular neoplasm that is commonly associated with AIDS. The pathogenesis of KS is not well understood. KS tumor cells grow poorly in vitro and require medium conditioned by retrovirus-infected T lymphocytes. We observed that conditioned medium (CM) from type II human T-cell leukemia virus (HTLV-II)-infected T cells (HTLV-II CM) induces conversion of endothelial cells (ECs) to a KS tumor cell-like phenotype. ECs grown in HTLV-II CM acquired a spindle-shaped morphology, the ability to express factor XIIIa and other KS cell markers, and a cytokine production profile similar to that of KS cells. We found that HTLV-II CM contains large quantities of scatter factor (SF), an angiogenic cytokine that stimulates cell motility. SF induced ECs to become spindle-shaped and express factor XIIIa. Moreover, SF was found to be a mitogen for KS cells in vitro and was identified within KS lesions in vivo. SF mRNA was present in KS cells in vitro, and antibodies against SF inhibited the growth of KS cells. The receptor for SF, the c-met protein, was expressed by ECs, dermal dendrocytes, and KS tumor cells in vitro and in vivo. HTLV-II CM was highly angiogenic in vivo, which was blocked by antibodies against SF. Based on these findings, we suggest that SF plays a role in the initiation and maintenance of KS lesions.
引用
收藏
页码:5281 / 5285
页数:5
相关论文
共 36 条
[1]  
ADAMS JC, 1991, J CELL SCI, V98, P385
[2]  
BHARGAVA M, 1992, CELL GROWTH DIFFER, V3, P11
[3]   IDENTIFICATION OF THE HEPATOCYTE GROWTH-FACTOR RECEPTOR AS THE C-MET PROTOONCOGENE PRODUCT [J].
BOTTARO, DP ;
RUBIN, JS ;
FALETTO, DL ;
CHAN, AML ;
KMIECIK, TE ;
VANDEWOUDE, GF ;
AARONSON, SA .
SCIENCE, 1991, 251 (4995) :802-804
[4]   HEPATOCYTE GROWTH-FACTOR IS A POTENT ANGIOGENIC FACTOR WHICH STIMULATES ENDOTHELIAL-CELL MOTILITY AND GROWTH [J].
BUSSOLINO, F ;
DIRENZO, MF ;
ZICHE, M ;
BOCCHIETTO, E ;
OLIVERO, M ;
NALDINI, L ;
GAUDINO, G ;
TAMAGNONE, L ;
COFFER, A ;
COMOGLIO, PM .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :629-641
[5]   PREVENTION OF PRE-PCR MIS-PRIMING AND PRIMER DIMERIZATION IMPROVES LOW-COPY-NUMBER AMPLIFICATIONS [J].
CHOU, Q ;
RUSSELL, M ;
BIRCH, DE ;
RAYMOND, J ;
BLOCH, W .
NUCLEIC ACIDS RESEARCH, 1992, 20 (07) :1717-1723
[6]   KAPOSIS SARCOMA REVISITED [J].
DORFMAN, RF .
HUMAN PATHOLOGY, 1984, 15 (11) :1013-1017
[7]   ANGIOGENESIS IN PSORIASIS - THERAPEUTIC IMPLICATIONS [J].
FOLKMAN, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1972, 59 (01) :40-&
[8]   CHARACTERIZATION OF THE TPR-MET ONCOGENE-P65 AND THE MET PROTOONCOGENE-P140 PROTEIN-TYROSINE KINASES [J].
GONZATTIHACES, M ;
SETH, A ;
PARK, M ;
COPELAND, T ;
OROSZLAN, S ;
VANDEWOUDE, GF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (01) :21-25
[9]   SCATTER FACTOR INDUCES BLOOD-VESSEL FORMATION INVIVO [J].
GRANT, DS ;
KLEINMAN, HK ;
GOLDBERG, ID ;
BHARGAVA, MM ;
NICKOLOFF, BJ ;
KINSELLA, JL ;
POLVERINI, P ;
ROSEN, EM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1937-1941
[10]   IDENTIFICATION OF INTRACELLULAR FACTOR-XIII IN HUMAN-MONOCYTES AND MACROPHAGES [J].
HENRIKSSON, P ;
BECKER, S ;
LYNCH, G ;
MCDONAGH, J .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (02) :528-534