首页> 外文期刊>Cell and Tissue Research >Spatiotemporal expression pattern of DsRedT3/CCK gene construct during postnatal development of myenteric plexus in transgenic mice.
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Spatiotemporal expression pattern of DsRedT3/CCK gene construct during postnatal development of myenteric plexus in transgenic mice.

机译:DsRedT3 / CCK基因构建体在转基因小鼠肌间神经丛产后发育过程中的时空表达模式。

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摘要

Cholecystokinin (CCK) is an early marker of both neuronal and endocrine cell lineages in the developing gastrointestinal tract. To determine the quantitative properties and the spatial distribution of the CCK-expressing myenteric neurones in early postnatal life, a transgenic mouse strain with a CCK promoter-driven red fluorescent protein (DsRedT3/CCK) was established. The cell-specific expression of DsRedT3/CCK was validated by in situ hybridization with a CCK antisense riboprobe and by in situ hybridization coupled with immunohistochemistry involving a monoclonal antibody to CCK. A gradual increase in the DsRedT3/CCK-expressing enteric neurones with clear regional differences was documented from birth until the suckling to weaning transition, in parallel with the period of rapid intestinal growth and functional maturation. To evaluate the proportion of myenteric neurones in which DsRedT3/CCK transgene expression was colocalized with the enteric neuronal marker peripherin, immunofluorescence techniques were applied. All DsRedT3/CCK neurones were peripherin-immunoreactive and the proportion of DsRedT3/CCK-expressing myenteric neurones in the duodenum was the highest after the third week of life, when the number of peripherin-immunoreactive myenteric neurones in this region had decreased. Nearly all of the DsRedT3/CCK-expressing neurones also expressed 5-hydroxytryptophan (5-HT). Thus, by utilizing a new transgenic mouse strain, we have demonstrated a small number of CCK-expressing myenteric neurones with a developmentally regulated spatiotemporal distribution. The coexistence of CCK and 5-HT in the majority of these neurones suggests their possible regulatory role in feeding at the suckling to weaning transition.
机译:胆囊收缩素(CCK)是发育中胃肠道中神经元和内分泌细胞谱系的早期标记。为了确定产后早期表达CCK的肠系膜神经元的定量特性和空间分布,建立了具有CCK启动子驱动的红色荧光蛋白(DsRedT3 / CCK)的转基因小鼠品系。 DsRedT3 / CCK的细胞特异性表达通过与CCK反义核糖核酸探针的原位杂交,以及与涉及CCK单克隆抗体的免疫组织化学结合的原位杂交来验证。从出生到哺乳到断奶过渡,与肠道快速生长和功能成熟的时期平行,表达DsRedT3 / CCK的肠道神经元逐渐增加,区域差异明显。为了评估其中DsRedT3 / CCK转基因表达与肠神经元标记外围蛋白共定位的肌层神经元的比例,采用了免疫荧光技术。所有DsRedT3 / CCK神经元均具有外周蛋白免疫反应性,而出生后第三周,十二指肠中表达DsRedT3 / CCK的肌层神经元的比例最高,这时该区域的外周蛋白免疫反应性肌层神经元数量减少。几乎所有表达DsRedT3 / CCK的神经元也表达5-羟色氨酸(5-HT)。因此,通过利用新的转基因小鼠品系,我们已经证明了少量的CCK表达的肠系膜神经元具有发育调控的时空分布。在大多数这些神经元中,CCK和5-HT的共存表明它们在哺乳期至断奶期的进食中可能具有调节作用。

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