Physicochemical Activation of Recombinant Latent Transforming Growth Factor-beta's 1, 2, and 3

被引:334
作者
Brownh, Peter D. [1 ]
Wakefiel, Lalage M. [1 ]
Levinson, Arthur D. [2 ]
Sporn, Michael B. [1 ]
机构
[1] NCI, Chemoprevent Lab, Bldg 41,Room C629, Bethesda, MD 20892 USA
[2] Genentech Inc, Dept Cell Genet, San Francisco, CA 94080 USA
关键词
transforming growth factor-beta; latent complexes; recombinant methods;
D O I
10.3109/08977199009037500
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Native and recombinant forms of transforming growth factor-beta 1 (TGF-beta 1) are synthesized predominantly as biologically latent complexes. Physicochemical analysis demonstrates that the more recently described TGF-beta 2 and TGF-beta 3 are also latent, and reveals a common series of sharply defined parameters for activation. Human recombinant latent TGF-beta's 1 and 2 show identical profiles of activation by acid and base; the transition from latency occurs between pH 4.1 and 3.1, and between pH 11.0 and 11.9. The profile for chicken recombinant latent TGF-beta 3 is slightly shifted with activation between pH 3.1 and 2.5, and between pH 10.0 and 12.3. Thermal activation of native and recombinant latent TGF-beta 1 occurs over the temperature ranges of 75-100 degrees C and 65-100 degrees C, respectively, with complete activation after 5 min at 8 degrees C. Temperatures above 90 degrees C result in thermal denaturation of TGF-beta 1 itself. Recombinant latent TGF-beta's 2 and 3 are also activated over this temperature range; however, maximum activation occurs at 100 degrees C. These results suggest common elements in latent complex structure despite differences between the TGF-beta subtypes in pro-region primary sequence.
引用
收藏
页码:35 / 43
页数:10
相关论文
共 23 条
[1]   AN ACTIVATED FORM OF TRANSFORMING GROWTH FACTOR-BETA IS PRODUCED BY COCULTURES OF ENDOTHELIAL-CELLS AND PERICYTES [J].
ANTONELLIORLIDGE, A ;
SAUNDERS, KB ;
SMITH, SR ;
DAMORE, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4544-4548
[2]   IMMUNODETECTION AND QUANTITATION OF THE 2 FORMS OF TRANSFORMING GROWTH FACTOR-BETA (TGF-BETA-1 AND TGF-BETA-2) SECRETED BY CELLS IN CULTURE [J].
DANIELPOUR, D ;
DART, LL ;
FLANDERS, KC ;
ROBERTS, AB ;
SPORN, MB .
JOURNAL OF CELLULAR PHYSIOLOGY, 1989, 138 (01) :79-86
[3]   COMPLEMENTARY-DNA FOR HUMAN GLIOBLASTOMA-DERIVED T-CELL SUPPRESSOR FACTOR, A NOVEL MEMBER OF THE TRANSFORMING GROWTH FACTO-BETA GENE FAMILY [J].
DEMARTIN, R ;
HAENDLER, B ;
HOFERWARBINEK, R ;
GAUGITSCH, H ;
WRANN, M ;
SCHLUSENER, H ;
SEIFERT, JM ;
BODMER, S ;
FONTANA, A ;
HOFER, E .
EMBO JOURNAL, 1987, 6 (12) :3673-3677
[4]   COMPLEMENTARY DEOXYRIBONUCLEIC-ACID CLONING OF A NOVEL TRANSFORMING GROWTH FACTOR-BETA MESSENGER RIBONUCLEIC-ACID FROM CHICK-EMBRYO CHONDROCYTES [J].
JAKOWLEW, SB ;
DILLARD, PJ ;
KONDAIAH, P ;
SPORN, MB ;
ROBERTS, AB .
MOLECULAR ENDOCRINOLOGY, 1988, 2 (08) :747-755
[5]   CONVERSION OF A HIGH-MOLECULAR-WEIGHT LATENT BETA-TGF FROM CHICKEN-EMBRYO FIBROBLASTS INTO A LOW-MOLECULAR-WEIGHT ACTIVE BETA-TGF UNDER ACIDIC CONDITIONS [J].
LAWRENCE, D ;
PIRCHER, R ;
JULLIEN, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 133 (03) :1026-1034
[6]   PROTEOLYTIC ACTIVATION OF LATENT TRANSFORMING GROWTH FACTOR-BETA FROM FIBROBLAST-CONDITIONED MEDIUM [J].
LYONS, RM ;
KESKIOJA, J ;
MOSES, HL .
JOURNAL OF CELL BIOLOGY, 1988, 106 (05) :1659-1665
[7]  
Maniatis T., 1982, MOL CLONING LAB MANU
[8]   THE TGF-BETA FAMILY OF GROWTH AND DIFFERENTIATION FACTORS [J].
MASSAGUE, J .
CELL, 1987, 49 (04) :437-438
[9]   ROLE FOR CARBOHYDRATE STRUCTURES IN TGF-BETA-1 LATENCY [J].
MIYAZONO, K ;
HELDIN, CH .
NATURE, 1989, 338 (6211) :158-160
[10]  
MIYAZONO K, 1988, J BIOL CHEM, V263, P6407