Univ. Lille, CNRS, Institut Pasteur de Lille, UMR 8199-EGID, 59000, Lille, France.
Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520, IEMN, 59000, Lille, France.
Cell Mol Life Sci. 2021 Jan;78(1):287-298. doi: 10.1007/s00018-020-03499-7. Epub 2020 Mar 18.
Unveiling the key pathways underlying postnatal beta-cell proliferation can be instrumental to decipher the mechanisms of beta-cell mass plasticity to increased physiological demand of insulin during weight gain and pregnancy. Using transcriptome and global Serine Threonine Kinase activity (STK) analyses of islets from newborn (10 days old) and adult rats, we found that highly proliferative neonatal rat islet cells display a substantially elevated activity of the mitogen activated protein 3 kinase 12, also called dual leucine zipper-bearing kinase (Dlk). As a key upstream component of the c-Jun amino terminal kinase (Jnk) pathway, Dlk overexpression was associated with increased Jnk3 activity and was mainly localized in the beta-cell cytoplasm. We provide the evidence that Dlk associates with and activates Jnk3, and that this cascade stimulates the expression of Ccnd1 and Ccnd2, two essential cyclins controlling postnatal beta-cell replication. Silencing of Dlk or of Jnk3 in neonatal islet cells dramatically hampered primary beta-cell replication and the expression of the two cyclins. Moreover, the expression of Dlk, Jnk3, Ccnd1 and Ccnd2 was induced in high replicative islet beta cells from ob/ob mice during weight gain, and from pregnant female rats. In human islets from non-diabetic obese individuals, DLK expression was also cytoplasmic and the rise of the mRNA level was associated with an increase of JNK3, CCND1 and CCND2 mRNA levels, when compared to islets from lean and obese patients with diabetes. In conclusion, we find that activation of Jnk3 signalling by Dlk could be a key mechanism for adapting islet beta-cell mass during postnatal development and weight gain.
揭示出生后胰岛β细胞增殖的关键途径,有助于解析β细胞质量对胰岛素生理需求增加的可塑性机制,例如在体重增加和妊娠期间。通过对新生(10 天大)和成年大鼠胰岛的转录组和全局丝氨酸苏氨酸激酶活性(STK)分析,我们发现高增殖的新生大鼠胰岛细胞表现出明显升高的有丝分裂原激活蛋白激酶 12(MAPK12),也称为双亮氨酸拉链激酶(Dlk)活性。作为 c-Jun 氨基末端激酶(Jnk)途径的关键上游成分,Dlk 过表达与 Jnk3 活性增加相关,并且主要定位于β细胞细胞质中。我们提供的证据表明,Dlk 与 Jnk3 相关联并激活 Jnk3,该级联反应刺激 Ccnd1 和 Ccnd2 的表达,这两种细胞周期蛋白对于出生后β细胞复制至关重要。在新生胰岛细胞中沉默 Dlk 或 Jnk3 会严重阻碍初级β细胞复制和这两种细胞周期蛋白的表达。此外,在 ob/ob 小鼠体重增加期间和怀孕雌性大鼠的高复制胰岛β细胞中诱导了 Dlk、Jnk3、Ccnd1 和 Ccnd2 的表达。在非糖尿病肥胖个体的人胰岛中,DLK 表达也在细胞质中,与瘦人和肥胖糖尿病患者的胰岛相比,其 mRNA 水平的升高与 JNK3、CCND1 和 CCND2 mRNA 水平的升高相关。总之,我们发现 Dlk 激活 Jnk3 信号可能是适应出生后发育和体重增加期间胰岛β细胞质量的关键机制。