Nosaka Tetsuya, Morita Sumiyo, Kitamura Hidetomo, Nakajima Hideaki, Shibata Fumi, Morikawa Yoshihiro, Kataoka Yuki, Ebihara Yasuhiro, Kawashima Toshiyuki, Itoh Tsuneo, Ozaki Katsutoshi, Senba Emiko, Tsuji Kohichiro, Makishima Fusao, Yoshida Nobuaki, Kitamura Toshio
Division of Hematopoietic Factors, Advanced Clinical Research Center, Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan.
Mol Cell Biol. 2003 Apr;23(8):2969-80. doi: 10.1128/MCB.23.8.2969-2980.2003.
Dorsoventral patterning depends on the local concentrations of the morphogens. Twisted gastrulation (TSG) regulates the extracellular availability of a mesoderm inducer, bone morphogenetic protein 4 (BMP-4). However, TSG function in vivo is still unclear. We isolated a TSG cDNA as a secreted molecule from the mouse aorta-gonad-mesonephros region. Here we show that TSG-deficient mice were born healthy, but more than half of the neonatal pups showed severe growth retardation shortly after birth and displayed dwarfism with delayed endochondral ossification and lymphopenia, followed by death within a month. TSG-deficient thymus was atrophic, and phosphorylation of SMAD1 was augmented in the thymocytes, suggesting enhanced BMP-4 signaling in the thymus. Since BMP-4 promotes skeletogenesis and inhibits thymus development, our findings suggest that TSG acts as both a BMP-4 agonist in skeletogenesis and a BMP-4 antagonist in T-cell development. Although lymphopenia in TSG-deficient mice would partly be ascribed to systemic effects of runtiness and wasting, our findings may also provide a clue for understanding the pathogenesis of human dwarfism with combined immunodeficiency.
背腹模式形成取决于形态发生素的局部浓度。扭曲原肠胚形成(TSG)调节中胚层诱导因子骨形态发生蛋白4(BMP - 4)的细胞外可用性。然而,TSG在体内的功能仍不清楚。我们从小鼠主动脉 - 性腺 - 中肾区域分离出一种作为分泌分子的TSG cDNA。在此我们表明,TSG基因缺陷小鼠出生时健康,但超过一半的新生幼崽在出生后不久出现严重生长迟缓,并表现出侏儒症,伴有软骨内成骨延迟和淋巴细胞减少,随后在一个月内死亡。TSG基因缺陷的胸腺萎缩,胸腺细胞中SMAD1的磷酸化增强,提示胸腺中BMP - 4信号增强。由于BMP - 4促进骨骼生成并抑制胸腺发育,我们的研究结果表明,TSG在骨骼生成中作为BMP - 4激动剂,而在T细胞发育中作为BMP - 4拮抗剂。虽然TSG基因缺陷小鼠的淋巴细胞减少部分可归因于矮小和消瘦的全身影响,但我们的研究结果也可能为理解伴有联合免疫缺陷的人类侏儒症的发病机制提供线索。