Crossman M W, Hauft S M, Gordon J I
Department of Molecular Biology, and Pharmacology, Washington University School of Medicine, St. Louis, Missouri 63110.
J Cell Biol. 1994 Sep;126(6):1547-64. doi: 10.1083/jcb.126.6.1547.
Normal, chimeric-transgenic, and transgenic mice have been used to study the axial patterns of ileal lipid-binding protein gene (Ilbp) expression during and after completion of gut morphogenesis. Ilbp is initially activated in enterocytes in bidirectional wave that expands proximally in the ileum and distally to the colon during late gestation and the first postnatal week. This activation occurs at the same time that a wave of cytodifferentiation of the gut endoderm is completing its unidirectional journey from duodenum to colon. The subsequent contraction of Ilbp's expression domain, followed by its reexpansion from the distal to proximal ileum, coincides with a critical period in gut morphogenesis (postnatal days 7-28) when its proliferative units (crypts) form, establish their final stem cell hierarchy, and then multiply through fission. The wave of reactivation is characterized by changing patterns of Ilbp expression: (a) at the proximal most boundary of the wave, villi contain a mixed population of scattered ileal lipid-binding protein (ILBP)-positive and ILBP-negative enterocytes derived from the same monoclonal crypt; (b) somewhat more distally, villi contain vertical coherent stripes of wholly ILBP-positive enterocytes derived from monoclonal crypts and adjacent, wholly ILBP-negative stripes of enterocytes emanating from other monoclonal crypts; and (c) more distally, all the enterocytes on a villus support Ilbp expression. Functional mapping studies of Ilbp's promoter in transgenic mice indicate that nucleotides -145 to +48 contain cis-acting elements sufficient to produce an appropriately directed distal-to-proximal wave of Ilbp activation in the ileum, to maintain an appropriate axial distribution of monophenotypic wholly reporter-positive villi in the distal portion of the ileum, as well as striped and speckled villi in the proximal portion of its expression domain, and to correctly support reporter production in villus-associated ileal enterocytes. Nucleotides -417 to -146 of Ilbp contain a "temporal" suppressor that delays initial ileal activation of the gene until the second postnatal week. Nucleotides -913 to -418 contain a temporal suppressor that further delays initial activation of the gene until the third to fourth postnatal week, a spatial suppressor that prohibits gene expression in the proximal quarter of the ileum and in the proximal colon, and a cell lineage suppressor that prohibits expression in goblet cells during the first two postnatal weeks.
正常小鼠、嵌合转基因小鼠和转基因小鼠已被用于研究肠道形态发生过程中及完成后回肠脂质结合蛋白基因(Ilbp)表达的轴向模式。Ilbp最初在肠细胞中以双向波的形式被激活,在妊娠后期和出生后的第一周,该波向回肠近端扩展并向远端延伸至结肠。这种激活发生在肠道内胚层细胞分化波从十二指肠向结肠完成单向行程的同时。随后,Ilbp表达域收缩,随后从回肠远端向近端重新扩展,这与肠道形态发生的关键时期(出生后第7 - 28天)相吻合,此时其增殖单位(隐窝)形成,建立最终的干细胞层级,然后通过裂变增殖。重新激活波的特征是Ilbp表达模式的变化:(a)在波的最近端边界,绒毛包含来自同一单克隆隐窝的散在的回肠脂质结合蛋白(ILBP)阳性和ILBP阴性肠细胞的混合群体;(b)在稍远端,绒毛包含来自单克隆隐窝的完全ILBP阳性肠细胞的垂直连贯条纹以及来自其他单克隆隐窝的相邻的完全ILBP阴性肠细胞条纹;(c)在更远端,绒毛上的所有肠细胞都支持Ilbp表达。对转基因小鼠中Ilbp启动子的功能图谱研究表明,核苷酸-145至+48包含顺式作用元件,足以在回肠中产生适当定向的从远端到近端的Ilbp激活波,以维持回肠远端单表型完全报告基因阳性绒毛以及其表达域近端的条纹状和斑点状绒毛的适当轴向分布,并正确支持绒毛相关回肠肠细胞中的报告基因产生。Ilbp的核苷酸-417至-146包含一个“时间”抑制子,可将该基因的初始回肠激活延迟至出生后第二周。核苷酸-913至-418包含一个时间抑制子,可进一步将该基因的初始激活延迟至出生后第三至第四周;一个空间抑制子,可阻止该基因在回肠近端四分之一和近端结肠中表达;以及一个细胞谱系抑制子,可在出生后的前两周阻止该基因在杯状细胞中表达。