首页> 美国卫生研究院文献>The Journal of Biological Chemistry >TLT-1s Alternative Transcripts of Triggering Receptor Expressed on Myeloid Cell-like Transcript-1 (TLT-1) Inhibits the Triggering Receptor Expressed on Myeloid Cell-2 (TREM-2)-mediated Signaling Pathway during Osteoclastogenesis
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TLT-1s Alternative Transcripts of Triggering Receptor Expressed on Myeloid Cell-like Transcript-1 (TLT-1) Inhibits the Triggering Receptor Expressed on Myeloid Cell-2 (TREM-2)-mediated Signaling Pathway during Osteoclastogenesis

机译:TLT-1s在髓样细胞样转录物-1(TLT-1)上表达的触发受体的替代转录物抑制在破骨细胞形成过程中在髓样细胞2(TREM-2)介导的信号传导通路上表达的触发受体。

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摘要

Triggering receptor expressed on myeloid cells (TREM)-like transcript-1 (TLT-1) is an immunoreceptor tyrosine-based inhibitory motif (ITIM)-baring TREM family protein. In this study, we identified an alternative transcript form of TLT-1, namely TLT-1s, which has very short extracellular immunoglobulin domain consisting of only 202 amino acids. TLT-1s was mainly expressed in macrophages and osteoclast precursor cells. Upon receptor activator of nuclear factor-κB ligand stimulation, TLT-1s mRNA and protein levels were gradually decreased in BMMs. We also showed the TLT-1s is localized to the cytoplasmic membrane in osteoclast precursor cells. TLT-1s silencing strongly enhanced the formation and resorption activity of osteoclast. In addition, forced expression of TLT-1s showed reduced formation of osteoclast. Because ITIM-baring proteins inhibit immunoreceptor tyrosine-based activation motif (ITAM)-mediated receptor signaling, we tested whether TLT-1s physically interacted with TREM-2, the ITAM-associated co-stimulatory receptor essential for osteoclast differentiation. We showed that TLT-1s is associated with TREM-2 in osteoclast precursor cells. TLT-1s is also associated with tyrosine Src homology 2 domain-containing phosphatase-1 and SH2 domain-containing inositol phosphatase-1 and recruited them to the TREM2-ITAM signaling complex. In addition, knockdown of TLT-1s markedly elevated the intracellular calcium concentration and oscillation in osteoclast precursor cells. In addition, calcium-mediated induction of nuclear factor of activated T cells was also increased by TLT-1s silencing. Furthermore, TREM-2-mediated Akt activation and proliferation of osteoclast precursor cells were also enhanced in TLT-1s silenced cells. In this paper, we found the noble ITIM-baring inhibitory membrane protein; TLT-1s, which regulates ITAM-mediated signaling on osteoclastogenesis.
机译:髓样细胞(TREM)样转录物1(TLT-1)上表达的触发受体是一种基于免疫受体酪氨酸的抑制性基序(ITIM)的TREM家族蛋白。在这项研究中,我们确定了TLT-1的另一种转录形式,即TLT-1s,它具有非常短的仅由202个氨基酸组成的细胞外免疫球蛋白结构域。 TLT-1s主要在巨噬细胞和破骨细胞前体细胞中表达。在核因子-κB配体刺激受体激活剂后,BMMs中TLT-1s的mRNA和蛋白水平逐渐降低。我们还显示了TLT-1位于破骨细胞前体细胞的细胞质膜上。 TLT-1s沉默大大增强了破骨细胞的形成和吸收活性。此外,TLT-1s的强制表达显示破骨细胞形成减少。因为ITIM裸蛋白抑制免疫受体酪氨酸激活基序(ITAM)介导的受体信号传导,所以我们测试了TLT-1是否与TREM-2物理相互作用,TREM-2是破骨细胞分化所必需的ITAM相关共刺激受体。我们显示,破骨细胞前体细胞中TLT-1与TREM-2相关。 TLT-1s还与酪氨酸Src同源性2结构域的磷酸酶-1和SH2结构域的肌醇磷酸酶-1相关,并将它们募集到TREM2-ITAM信号复合体中。此外,TLT-1的敲低显着提高了破骨细胞前体细胞的细胞内钙浓度和振荡。此外,TLT-1s沉默也增强了钙介导的活化T细胞核因子的诱导。此外,在TLT-1s沉默的细胞中,破骨细胞前体细胞的TREM-2介导的Akt活化和增殖也得到增强。在本文中,我们发现了高贵的ITIM-baring抑制膜蛋白。 TLT-1s,它调节破骨细胞生成的ITAM介导的信号传导。

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