c-fos and c-jun mRNA expression in activated cord and adult lymphocytes: An analysis by northern hybridization

被引:0
作者
DePalma, L
Brown, E
Baker, R
机构
[1] George Washington Univ, Med Ctr, Div Clin Pathol, Dept Pathol, Washington, DC 20037 USA
[2] George Washington Univ, Med Ctr, Dept Anat & Cell Biol, Washington, DC USA
[3] Fairfax Hosp, Falls Church, VA 22046 USA
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives: To further analyze the neonatal immune response to an antigenic challenge such as blood transfusion, c-fos and c-jun mRNA expression were analyzed in twelve in-vitro-stimulated normal cord blood and ten in-vitro-stimulated normal adult peripheral blood lymphocyte samples. Materials and Methods: Lymphocyte samples were stimulated by either the mitogen phytohemagglutinin (PHA) or the monoclonal antibody alpha CD3. Proliferation rate and Northern blot hybridization were employed. Results: Cord lymphocytes revealed a greater proliferation rate with PHA and alpha CD3 than adult lymphocytes (p = 0.0081 and 0.0023, respectively). In addition, Northern blot analysis of cord and adult samples revealed similar maximal increases in c-fos (99 +/- 15 and 126 +/- 11%, p = 0.0126) and c-jun (123 +/- 9 and 185 +/- 38%, p = 0.0291) mRNA expression, respectively, as early as 15 min post-alpha CD3 stimulation. Adult lymphocytes showed an equivalent increase in mRNA expression of c-fos and c-jun (140 +/- 25 and 155 +/- 31%) at 30 min post-PHA stimulation, while cord lymphocyte maximum c-fos and c-jun expression (82 +/- 6 and 142 +/- 12%) occurred at 15 min post-PHA stimulation (c-fos, p = 0.0354; c-jun, p = 0.0112). Conclusion: Although cord lymphocyte proliferation rates were significantly greater than those of adult lymphocytes following stimulation, lymphocyte activation, as analyzed by c-fos and c-jun mRNA expression, appears similar in both cord and adult samples. We conclude that cord lymphocyte activation exhibits an adult-type profile.
引用
收藏
页码:134 / 138
页数:5
相关论文
共 16 条
[1]  
Altman A, 1990, Adv Immunol, V48, P227, DOI 10.1016/S0065-2776(08)60756-7
[2]   IMMUNOLOGY OF THE NEONATE [J].
BURGIO, GR ;
UGAZIO, AG ;
NOTARANGELO, LD .
CURRENT OPINION IN IMMUNOLOGY, 1990, 2 (05) :770-777
[3]   THE C-FOS PROTEIN INTERACTS WITH C-JUN/AP-1 TO STIMULATE TRANSCRIPTION OF AP-1 RESPONSIVE GENES [J].
CHIU, R ;
BOYLE, WJ ;
MEEK, J ;
SMEAL, T ;
HUNTER, T ;
KARIN, M .
CELL, 1988, 54 (04) :541-552
[4]   ANALYSIS OF T-HELPER AND ANTIGEN-PRESENTING CELL FUNCTIONS IN CORD BLOOD AND PERIPHERAL-BLOOD LEUKOCYTES FROM HEALTHY-CHILDREN OF DIFFERENT AGES [J].
CLERICI, M ;
DEPALMA, L ;
ROILIDES, E ;
BAKER, R ;
SHEARER, GM .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (06) :2829-2836
[5]   PRESENCE OF THE RED-CELL ALLOANTIBODY ANTI-E IN AN 11-WEEK-OLD INFANT [J].
DEPALMA, L ;
CRISS, VR ;
ROSEFF, SD ;
LUBAN, NLC .
TRANSFUSION, 1992, 32 (02) :177-179
[6]   THE NEONATAL IMMUNE-RESPONSE TO WASHED AND IRRADIATED RED-CELLS - LACK OF EVIDENCE OF LYMPHOCYTE-ACTIVATION [J].
DEPALMA, L ;
DUNCAN, B ;
CHAN, MM ;
LUBAN, NLC .
TRANSFUSION, 1991, 31 (08) :737-742
[7]  
DEPALMA L, 1994, SCI BASIS TRANSFUSIO, P443
[8]   DIFFERENTIATION OF T-CELL LYMPHOKINE GENE-EXPRESSION - THE INVITRO ACQUISITION OF T-CELL MEMORY [J].
EHLERS, S ;
SMITH, KA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (01) :25-36
[9]   MITOGEN-INDUCED GENES ARE SUBJECT TO MULTIPLE PATHWAYS OF REGULATION IN THE INITIAL-STAGES OF T-CELL ACTIVATION [J].
IRVING, SG ;
JUNE, CH ;
ZIPFEL, PF ;
SIEBENLIST, U ;
KELLY, K .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (03) :1034-1040
[10]  
LEVIN WJ, 1995, ONCOGENE, V11, P1261