THE EFFECT OF RETINOIC ACID ON GROWTH AND PROTOONCOGENE EXPRESSION IN HAMSTER TRACHEAL EPITHELIAL-CELLS

被引:16
作者
NILES, RM
LOEWY, BP
BROWN, K
机构
[1] Department of Biochemistry, Boston University School of Medicine, 02118., MA
关键词
D O I
10.1165/ajrcmb/2.4.365
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
Retinoic acid (RA) has been shown to be required for the maintenance of epithelial differentiation. Vitamin A deficiency in hamsters induces the tracheal epithelial cells to undergo squamous metaplasia. Reversing the vitamin deficiency restores the tracheal epithelial cells to their normal morphology and function. Using a hamster tracheal epithelial (HTE) cell culture system which undergoes differentiation to predominantly secretory cells in vitro, we found that RA can convert flat, squamous-like cells to compact, cuboidal-like cells, and that it stimulated cell proliferation. The mitogenic response to RA was maximal at 10(-7) M and required at least 48 h of treatment to observe the effect. RNA levels of growth-related genes during the growth and differentiation phases of primary HTE cultures were examined by Northern analysis. RA maintained a high level of c-myc RNA expression in preconfluent cultures, whereas untreated cells had low amounts of c-myc RNA. Expression of RNA for the replication-dependent histone 3.2 followed a similar pattern, i.e., its level was high in retinoid-treated versus control preconfluent cultures. In confluent (fully differentiated) HTE cell cultures, both retinoid-treated and control cells had low RNA levels of c-myc and histone 3.2. c-fos RNA levels were undetectable in either control or treated cells at any stage during primary culture. The RNA level of c-Ha-ras was very low in both control and treated cultures and did not vary with the state of growth or differentiation, except that when RA-treated cultures reached confluence, no c-Ha-ras RNA was detected.(ABSTRACT TRUNCATED AT 250 WORDS)
引用
收藏
页码:365 / 371
页数:7
相关论文
共 31 条
[1]   INDUCTION OF DIFFERENTIATION OF THE HUMAN PROMYELOCYTIC LEUKEMIA-CELL LINE (HL-60) BY RETINOIC ACID [J].
BREITMAN, TR ;
SELONICK, SE ;
COLLINS, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (05) :2936-2940
[2]   A METHOD FOR ISOLATION OF INTACT, TRANSLATIONALLY ACTIVE RIBONUCLEIC-ACID [J].
CATHALA, G ;
SAVOURET, JF ;
MENDEZ, B ;
WEST, BL ;
KARIN, M ;
MARTIAL, JA ;
BAXTER, JD .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1983, 2 (04) :329-335
[3]  
CHOPRA DP, 1982, J NATL CANCER I, V69, P895
[4]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[5]  
FILMUS J, 1985, CANCER RES, V45, P822
[6]   IDENTIFICATION OF A RECEPTOR FOR THE MORPHOGEN RETINOIC ACID [J].
GIGUERE, V ;
ONG, ES ;
SEGUI, P ;
EVANS, RM .
NATURE, 1987, 330 (6149) :624-629
[7]   STIMULATION OF 3T3 CELLS INDUCES TRANSCRIPTION OF THE C-FOS PROTO-ONCOGENE [J].
GREENBERG, ME ;
ZIFF, EB .
NATURE, 1984, 311 (5985) :433-438
[8]  
HARRIS CC, 1972, JNCI-J NATL CANCER I, V48, P743
[9]   REGULATION OF HUMAN HISTONE GENE-EXPRESSION - KINETICS OF ACCUMULATION AND CHANGES IN THE RATE OF SYNTHESIS AND IN THE HALF-LIVES OF INDIVIDUAL HISTONE MESSENGER-RNAS DURING THE HELA-CELL CYCLE [J].
HEINTZ, N ;
SIVE, HL ;
ROEDER, RG .
MOLECULAR AND CELLULAR BIOLOGY, 1983, 3 (04) :539-550
[10]  
HUANG FL, 1986, IN VITRO CELL DEV B, V22, P223