ORGANIZATION OF THE CRYPT-VILLUS AXIS AND EVOLUTION OF ITS STEM-CELL HIERARCHY DURING INTESTINAL DEVELOPMENT

被引:50
作者
HERMISTON, ML [1 ]
GORDON, JI [1 ]
机构
[1] WASHINGTON UNIV, SCH MED, DEPT MOLEC BIOL & PHARMACOL, ST LOUIS, MO 63110 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 1995年 / 268卷 / 05期
关键词
MOUSE GUT; EPITHELIAL CELL BIOLOGY;
D O I
10.1152/ajpgi.1995.268.5.G813
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The small intestinal crypt of the adult mouse represents a model system for studying cell renewal. One or more functionally equivalent stem cells located within the crypt fuel a continuous regeneration of the gut's four principal epithelial cell lineages. These lineages differentiate during a geographically well-organized migration along the crypt-villus axis. This axis does not complete its morphogenetic program until the third postnatal week. We examined the organization of the cryptvillus axis and its stem cell hierarchy in postnatal day 1 (P1) to P28 transgenic mice. These mice contained transcriptional regulatory elements from the liver fatty acid binding protein gene linked to a human growth hormone (hGH) reporter. Adult male and female animals exhibit a striped pattern of hGH accumulation in their villus-associated epithelial cells: vertical coherent bands of wholly hGH-positive epithelial cells derived from a monoclonal crypt and vertical coherent stripes of wholly hGH-negative epithelial cells derived from an adjacent crypt extend to the apical extrusion zone of their common villus. Villus striping develops in a proximal-to-distal wave that extends from the duodenum to the jejunum by P7 and to the ileum by P14. Striping occurs as a result of a loss in the ability to support transgene expression. The decision appears to affect all cells within a stripe, irrespective of their position along the basilar-to-apical axis of a villus, suggesting that it is programmed by the nascent crypt's multipotent stem cell(s). Suppression of transgene expression traverses the crypt-villus axis more rapidly than the rate of epithelial cell migration. The boundary between stripes is very sharp and does not contain cells with transitional levels of the hGH reporter, indicating that the epithelial components of the crypt-villus axis have a higher degree of organization at this stage of development than appreciated previously.
引用
收藏
页码:G813 / G822
页数:10
相关论文
共 40 条
[1]   CELL-KINETICS IN THE MOUSE SMALL-INTESTINE DURING IMMEDIATE POSTNATAL LIFE [J].
ALNAFUSSI, AI ;
WRIGHT, NA .
VIRCHOWS ARCHIV B-CELL PATHOLOGY INCLUDING MOLECULAR PATHOLOGY, 1982, 40 (01) :51-62
[2]   PANETH CELL-DIFFERENTIATION IN THE DEVELOPING INTESTINE OF NORMAL AND TRANSGENIC MICE [J].
BRY, L ;
FALK, P ;
HUTTNER, K ;
OUELLETTE, A ;
MIDTVEDT, T ;
GORDON, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (22) :10335-10339
[3]   MIGRATION OF FETAL INTESTINAL INTERVILLOUS CELLS IN NEONATAL MICE [J].
CALVERT, R ;
POTHIER, P .
ANATOMICAL RECORD, 1990, 227 (02) :199-206
[4]   ORIGIN, DIFFERENTIATION AND RENEWAL OF 4 MAIN EPITHELIAL-CELL TYPES IN MOUSE SMALL INTESTINE .1. COLUMNAR CELL [J].
CHENG, H ;
LEBLOND, CP .
AMERICAN JOURNAL OF ANATOMY, 1974, 141 (04) :461-&
[5]  
CHENG H, 1974, AM J ANAT, V141, P481, DOI 10.1002/aja.1001410404
[6]   WHOLE POPULATION CELL-KINETICS AND POSTNATAL-DEVELOPMENT OF THE MOUSE INTESTINAL EPITHELIUM [J].
CHENG, H ;
BJERKNES, M .
ANATOMICAL RECORD, 1985, 211 (04) :420-426
[7]   ORIGIN, DIFFERENTIATION AND RENEWAL OF 4 MAIN EPITHELIAL-CELL TYPES IN MOUSE SMALL INTESTINE .3. ENTERO-ENDOCRINE CELLS [J].
CHENG, H ;
LEBLOND, CP .
AMERICAN JOURNAL OF ANATOMY, 1974, 141 (04) :503-&
[8]  
CHENG H, 1974, AM J ANAT, V141, P521, DOI 10.1002/aja.1001410406
[9]   THE MOUSE ILEAL LIPID-BINDING PROTEIN GENE - A MODEL FOR STUDYING AXIAL PATTERNING DURING GUT MORPHOGENESIS [J].
CROSSMAN, MW ;
HAUFT, SM ;
GORDON, JI .
JOURNAL OF CELL BIOLOGY, 1994, 126 (06) :1547-1564
[10]   FETAL ENDODERM PRIMARILY HOLDS THE TEMPORAL AND POSITIONAL INFORMATION REQUIRED FOR MAMMALIAN INTESTINAL DEVELOPMENT [J].
DULUC, I ;
FREUND, JN ;
LEBERQUIER, C ;
KEDINGER, M .
JOURNAL OF CELL BIOLOGY, 1994, 126 (01) :211-221