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发育中胃肠道细胞增殖研究的模型

Models for the study of cell proliferation in the developing gastrointestinal tract.

作者信息

Klein R M

出版信息

J Pediatr Gastroenterol Nutr. 1986 Jul-Aug;5(4):513-7. doi: 10.1097/00005176-198607000-00001.

DOI:10.1097/00005176-198607000-00001
PMID:3735004
Abstract

Which is the best system to study in order to obtain data for the human developmental situation? While the temporal pattern of differentiation and growth in some of these species is similar to human development, there are major differences in terms of absorption of immunoglobulins. Humans and rabbits receive virtually complete passive immunity in utero, while rats receive partial immunity, and other species such as the calf, sheep, and pig receive virtually their complete passive immunity during the postnatal period. The morphological similarity of the neonatal rat and mouse small intestine to human fetal small intestine between 10 and 22 weeks adds some validity to the limited use of this model. However, the pattern of gastrointestinal differentiation late in gestation; the dependence on the postnatal period for the transfer of passive immunity; and the delayed closure of the gut are limiting factors in the use of this model comparison to the human situation. Although the opossum provides a useful model for the study of gastrointestinal development in a species with an extremely dependent, underdeveloped newborn and an extremely delayed closure of the gut, this situation is not analagous to the human fetal and neonatal pattern of gastrointestinal development. While animals such as the calf, pig, and sheep are morphologically similar to the human condition and exhibit a relatively short postnatal period of functional immunoglobulin uptake they are almost completely dependent upon the early postnatal period for transfer of passive immunity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了获取有关人类发育情况的数据,研究哪个系统是最佳选择?虽然其中一些物种的分化和生长时间模式与人类发育相似,但在免疫球蛋白吸收方面存在重大差异。人类和兔子在子宫内几乎获得完全的被动免疫,而大鼠获得部分免疫,其他物种如小牛、绵羊和猪在出生后时期几乎获得完全的被动免疫。新生大鼠和小鼠小肠与10至22周人类胎儿小肠的形态相似性为该模型的有限使用增添了一定的合理性。然而,妊娠后期胃肠道分化模式;被动免疫转移对出生后时期的依赖性;以及肠道关闭延迟,与人类情况相比,这些都是该模型使用中的限制因素。虽然负鼠为研究一种新生幼崽极度依赖、发育不全且肠道关闭极度延迟的物种的胃肠道发育提供了有用的模型,但这种情况与人类胎儿和新生儿胃肠道发育模式并不相似。虽然小牛、猪和绵羊等动物在形态上与人类情况相似,并且在出生后摄取功能性免疫球蛋白的时期相对较短,但它们几乎完全依赖出生后早期来转移被动免疫。(摘要截断于250字)

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