Crypt fission peaks early during infancy and crypt hyperplasia broadly peaks during infancy and childhood in the small intestine of humans

被引:45
作者
Cummins, Adrian G. [1 ]
Catto-Smith, Anthony G. [3 ]
Cameron, Donald J. [3 ]
Couper, Richard T. [2 ]
Davidson, Geoffrey P. [2 ]
Day, Andrew S. [4 ]
Hammond, Paul D. [2 ]
Moore, David J. [2 ]
Thompson, Fiona M. [1 ]
机构
[1] Queen Elizabeth Hosp, Dept Gastroenterol & Hepatol, Basil Hetzel Inst Med Res, Digest Dis Res Ctr, Woodville, SA 5011, Australia
[2] Univ Adelaide, Dept Paediat, Adelaide, SA 5005, Australia
[3] Royal Childrens Hosp, Dept Gastroenterol & Clin Nutr, Melbourne, Vic, Australia
[4] Sydney Childrens Hosp, Dept Gastroenterol, Sydney, NSW, Australia
关键词
crypt fission; crypt hyperplasia; growth; intestinal stem cell; small intestine;
D O I
10.1097/MPG.0b013e3181604d27
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Postnatal growth of the small intestine occurs by crypt hyperplasia and by the less recognised mechanism of crypt fission. How the small intestine grows is largely extrapolated from animals and is poorly described in humans. Aim: To investigate crypt fission and crypt hyperplasia as mechanisms of intestinal growth in humans. Patients and Methods: Proximal intestinal samples were taken from 3 neonates at surgical, anastomosis, and duodenal biopsies were taken at endoscopy from 16 infants (mean age 0.7, range 0.3-1.7 years), 14 children (mean age 7.9, range 2.4-16.2 years), and 39 adults. Morphometric measures of villous area, crypt length (measure of crypt hyperplasia), and percentage of bifid crypts (measure of crypt fission) were assessed by a microdissection technique. Results: Mean crypt fission rates in neonates, infants, children, and adults were 7.8%, 15%, 4.9%, and 1.7%, respectively. In particular, crypt fission peaked at 18% in 5 infants from 6 to 12 months of age. Mean crypt length was 123 mu m in neonates, 287 mu m in infants, 277 mu m in children, and 209 mu m in adults. Thus, crypt hyperplasia had a broad peak during infancy and childhood. Conclusions: We conclude that crypt fission was present predominantly during infancy, and crypt hyperplasia occurred during both infancy and childhood.
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收藏
页码:153 / 157
页数:5
相关论文
共 37 条
[1]   Molecular biology of the small intestine [J].
Ahuja, V ;
Dieckgraefe, BK ;
Anant, S .
CURRENT OPINION IN GASTROENTEROLOGY, 2006, 22 (02) :90-94
[2]   Upregulation of keratinocyte growth factor during T-cell immunity in the gut mucosa [J].
Bajaj-Elliott, M ;
Pender, SLF ;
Poulsom, R ;
MacDonald, TT .
INTESTINAL PLASTICITY IN HEALTH AND DISEASE, 1998, 859 :184-187
[3]  
BAKER SJ, 1962, INTESTINAL BIOPSY, P84
[4]   Activation of β-catenin in the stem cell region of crypts during growth of the small intestine in infant rats [J].
Camac, Kimberley S. ;
Thompson, Fiona M. ;
Cummins, Adrian G. .
DIGESTIVE DISEASES AND SCIENCES, 2007, 52 (05) :1242-1246
[5]   WHOLE POPULATION CELL-KINETICS AND POSTNATAL-DEVELOPMENT OF THE MOUSE INTESTINAL EPITHELIUM [J].
CHENG, H ;
BJERKNES, M .
ANATOMICAL RECORD, 1985, 211 (04) :420-426
[6]  
CLARKE RM, 1972, J ANAT, V112, P27
[7]   QUANTITATIVE HISTOLOGICAL STUDY OF ENTEROPATHY ASSOCIATED WITH HIV-INFECTION [J].
CUMMINS, AG ;
LABROOY, JT ;
STANLEY, DP ;
ROWLAND, R ;
SHEARMAN, DJC .
GUT, 1990, 31 (03) :317-321
[8]   Postnatal epithelial growth of the small intestine in the rat occurs by both crypt fission and crypt hyperplasia [J].
Cummins, AG ;
Jones, BJ ;
Thompson, FM .
DIGESTIVE DISEASES AND SCIENCES, 2006, 51 (04) :718-723
[9]   IMMUNE ACTIVATION DURING INFANCY IN HEALTHY HUMANS [J].
CUMMINS, AG ;
EGLINTON, BA ;
GONZALEZ, A ;
ROBERTON, DM .
JOURNAL OF CLINICAL IMMUNOLOGY, 1994, 14 (02) :107-115
[10]   Effect of breast milk and weaning on epithelial growth of the small intestine in humans [J].
Cummins, AG ;
Thompson, FM .
GUT, 2002, 51 (05) :748-754