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ZBTB20调节成年小鼠催乳素的表达和促乳素细胞功能。

ZBTB20 Regulates Prolactin Expression and Lactotrope Function in Adult Mice.

作者信息

Han Qing, Yan Xuede, Ye Yufei, Han Linhui, Ma Xianhua, Wang Ting, Cao Dongmei, Zhang Weiping J

机构信息

Department of Pathophysiology, Naval Medical University, Shanghai 200433, China.

NHC Key Laboratory of Hormones and Development, Chu Hsien-I Memorial Hospital and Tianjin Institute of Endocrinology, Tianjin Medical University, Tianjin 300134, China.

出版信息

Endocrinology. 2022 Oct 23;163(12). doi: 10.1210/endocr/bqac181.

Abstract

Lactotropes are prolactin (PRL)-secreting endocrine cells in the anterior pituitary. We have established the zinc finger protein ZBTB20 as an essential transcription factor for lactotrope specification, the disruption of which results in complete loss of lactotropes in mice. However, the potential role of ZBTB20 in mature lactotropes remains unclear. Here we demonstrate that ZBTB20 acts as a critical cell-autonomous regulator for PRL expression in mature lactotropes in adult mice. Via a CRISPR/Cas9 approach, we first generated a tamoxifen-inducible Prl-CreER knockin mouse line that could efficiently mediate gene recombination specifically in lactotropes. Conditional deletion of the Zbtb20 gene specifically in mature lactotropes at adulthood led to a substantial decrease in PRL levels both in the pituitary and in plasma, without significant alterations of lactotrope relative density in the pituitary from male or female mice. Furthermore, conditional disruption of Zbtb20 in adult female mice did not significantly change pregnancy-elicited lactotrope expansion, but caused an impaired mammary gland expansion and lactation due to the PRL defect. Thus, our data point to an important role of ZBTB20 in regulating PRL expression and lactotrope function at adulthood.

摘要

催乳素细胞是腺垂体中分泌催乳素(PRL)的内分泌细胞。我们已确定锌指蛋白ZBTB20是催乳素细胞特化的关键转录因子,破坏该因子会导致小鼠体内催乳素细胞完全缺失。然而,ZBTB20在成熟催乳素细胞中的潜在作用仍不清楚。在此我们证明,ZBTB20在成年小鼠的成熟催乳素细胞中作为PRL表达的关键细胞自主调节因子发挥作用。通过CRISPR/Cas9方法,我们首先构建了一种他莫昔芬诱导的Prl-CreER敲入小鼠品系,该品系能够有效地在催乳素细胞中特异性介导基因重组。成年期在成熟催乳素细胞中特异性条件性敲除Zbtb20基因,导致垂体和血浆中PRL水平大幅下降,而雄性或雌性小鼠垂体中催乳素细胞相对密度无显著变化。此外,成年雌性小鼠中Zbtb20的条件性破坏并未显著改变妊娠引起的催乳素细胞扩张,但由于PRL缺陷导致乳腺扩张和泌乳受损。因此,我们的数据表明ZBTB20在成年期调节PRL表达和催乳素细胞功能中起重要作用。

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