Peptide transporter function and prolidase activities in Caco-2 cells: A lack of coordinated expression

被引:8
作者
Hu, M [1 ]
Zheng, LX [1 ]
Chen, JY [1 ]
Liu, LJ [1 ]
Li, YQ [1 ]
Dantzig, AH [1 ]
Stratford, RE [1 ]
机构
[1] ELI LILLY & CO, LILLY RES LABS, LILLY CORP CTR, INDIANAPOLIS, IN 46285 USA
关键词
transcellular transport; intracellular metabolism; peptide transporter; peptidase; prolidase; dipeptide;
D O I
10.3109/10611869509015958
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Peptide transport and prolidase activities were measured to determine whether the expression of these two components of protein nutrition are coordinately regulated; i.e., whether an increase in the peptide transporter function will necessarily lead to a higher prolidase activity, or vice versa. The results indicated that peptide transporter function and prolidase activity respond differently to cell differentiation and feeding schedules. The results also indicated that peptide transport and prolidase activities were different in two Caco-2 cell ''clones'', with S-K cells transported peptides at higher rates but had lower total prolidase activities, when compared to ATCC cells. These results suggest that the expression of the peptide transporter function and prolidase activity is not coordinated. In addition, both the transporter and the prolidase activities affected the overall transport of Phe when given as the dipeptide Phe-Pro, supporting the notion that intestinal absorption of peptides is an essential component of amino acid absorption. In conclusion, the evidence suggests that the peptide transporter function and prolidase activity are not coordinately expressed by the human intestinal Caco-2 cells.
引用
收藏
页码:291 / 300
页数:10
相关论文
共 33 条
[1]  
Adibi S. A., 1981, PHYSL GASTROINTESTIN, P1073
[2]   UTILIZATION OF PEPTIDE CARRIER SYSTEM TO IMPROVE INTESTINAL-ABSORPTION - TARGETING PROLIDASE AS A PRODRUG-CONVERTING ENZYME [J].
BAI, JPF ;
HU, M ;
SUBRAMANIAN, P ;
MOSBERG, HI ;
AMIDON, GL .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1992, 81 (02) :113-116
[3]  
BORCHARDT RT, 1991, NATO ADV SCI I A-LIF, V218, P1
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   EXPRESSION AND PROTEIN-KINASE C-DEPENDENT REGULATION OF PEPTIDE/H+ COTRANSPORT SYSTEM IN THE CACO-2 HUMAN COLON-CARCINOMA CELL-LINE [J].
BRANDSCH, M ;
MIYAMOTO, Y ;
GANAPATHY, V ;
LEIBACH, FH .
BIOCHEMICAL JOURNAL, 1994, 299 :253-260
[6]   CHARACTERIZATION OF A NEWLY ISOLATED CACO-2 CLONE (TC-7), AS A MODEL OF TRANSPORT PROCESSES AND BIOTRANSFORMATION OF DRUGS [J].
CARO, I ;
BOULENC, X ;
ROUSSET, M ;
MEUNIER, V ;
BOURRIE, M ;
JULIAN, B ;
JOYEUX, H ;
ROGUES, C ;
BERGER, Y ;
ZWEIBAUM, A ;
FABRE, G .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1995, 116 (02) :147-158
[7]  
CHEESEMAN CI, 1991, PROG BIOPHYS MOL BIO, V55, P71, DOI 10.1016/0079-6107(91)90001-9
[8]   ROLE OF AMINO-ACID-TRANSPORT AND COUNTERTRANSPORT IN NUTRITION AND METABOLISM [J].
CHRISTENSEN, HN .
PHYSIOLOGICAL REVIEWS, 1990, 70 (01) :43-77
[9]   ASSOCIATION OF INTESTINAL PEPTIDE-TRANSPORT WITH A PROTEIN RELATED TO THE CADHERIN SUPERFAMILY [J].
DANTZIG, AH ;
HOSKINS, J ;
TABAS, LB ;
BRIGHT, S ;
SHEPARD, RL ;
JENKINS, IL ;
DUCKWORTH, DC ;
SPORTSMAN, JR ;
MACKENSEN, D ;
ROSTECK, PR ;
SKATRUD, PL .
SCIENCE, 1994, 264 (5157) :430-433
[10]   TRANSPORT MECHANISMS RESPONSIBLE FOR THE ABSORPTION OF LORACARBEF, CEFIXIME, AND CEFUROXIME AXETIL INTO HUMAN INTESTINAL CACO-2 CELLS [J].
DANTZIG, AH ;
DUCKWORTH, DC ;
TABAS, LB .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1994, 1191 (01) :7-13