نتایج جستجو برای: ژن ship2
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مقدمه: مقاومت به انسولین یک وضعیت پاتولوژیکی است که میزان انسولین طبیعی خون قادر به ایجاد پاسخ بیولوژیکی طبیعی نیست. این کاهش پاسخ میتواند تمام اثرات متابولیک انسولین را متاثر سازد. فسفاتازها ازجمله پروتئین تیروزین فسفاتازها ( protein-tyrosine phosphatase 1b (ptp1b) ، leukocyte common antigen-related protein (lar) ، ptp-sigma، ptp-α، shp-2) گروهی از آنزیمها هستند که نقش مهمی در کنترل مسیر ان...
مقدمه: دیسلیپیدمی به عنوان یکی از فاکتورهای خطر بیماریهای قلبی عروقی در افراد دیابتی مطرح میباشد. دیسلیپیدمی به وسیله افزایش غلظت تریگلیسرید پلاسما، کاهش hdl کلسترول و افزایش ldl به خصوص small dense ldl تشخیص داده میشود. شواهد متعدد از مطالعات انسانی و حیوانی بیانگر نقش مقاومت به انسولین به عنوان علت اصلی افزایش تریگلیسرید در بیماران دیابتی و افراد مبتلا به سندرم متابولیک میباشد. لیپوژنز ک...
The Src homology 2-containing inositol phosphatase SHIP1 functions in hemopoietic cells to limit activation events mediated by PI3K products, including Akt activation and cell survival. In contrast to the limited cellular expression of SHIP1, the related isoform SHIP2, is widely expressed in both parenchymal and hemopoietic cells. The goal of this study was to determine how SHIP2 functions to r...
Inositol phosphatases play an important role in regulation of cellular levels of lipid second messengers. Recently we have reported a novel function for SHIP2 in cell adhesion and spreading. In this study, we further characterize the adhesion-dependent tyrosine phosphorylation of SHIP2 and examine the role of Src family tyrosine kinases in the regulation of SHIP2 function. SHIP2 was tyrosine ph...
Phosphoinositides, particularly phosphatidylinositol (3,4,5)-trisphosphate [PI(3,4,5)P3] and phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2], are recognized by SHIP2 (also known as INPPL1) a member of the inositol polyphosphate 5-phosphatase family. SHIP2 dephosphorylates PI(3,4,5)P3 to form PI(3,4)P2; the latter interacts with specific target proteins (e.g. lamellipodin). Although the prefer...
PtdIns(3,4,5)P3 and PtdIns(3,4)P2 are major signalling molecules in mammalian cell biology. PtdIns(3,4)P2 can be produced by PI3Ks [PI (phosphoinositide) 3-kinases], but also by PI 5-phosphatases including SHIP2 [SH2 (Src homology 2)-domain-containing inositol phosphatase 2]. Proteomic studies in human cells revealed that SHIP2 can be phosphorylated at more than 20 sites, but their individual f...
Past studies have shown that the Src homology 2-containing inositol 5-phosphatase 2 (SHIP2) is commonly downregulated in gastric cancer, which contributes to elevated activation of PI3K/Akt signaling, proliferation and tumorigenesis of gastric cancer cells. However, the mechanisms underlying the reduced expression of SHIP2 in gastric cancer remain unclear. While gene copy number variation analy...
Phosphoinositol phosphatases are important regulators of signaling pathways relevant to both diabetes and cancer. A 3'-phosphoinositol phosphatase, phosphatase homologous to tensin (PTEN), is both a tumor suppressor and a negative regulator of insulin action. A 5'-phosphoinositol phosphatase, SH2-containing 5'-inositol phosphatase (SHIP2), regulates insulin signaling and its genetic knockout pr...
The lipid phosphatase SH2 domain-containing lipid phosphatase (SHIP2) has been implicated in the regulation of insulin sensitivity, but its role in the therapy of insulin-resistant states remains to be defined. Here, we examined the effects of an antisense oligonucleotide (AS) therapy directed against SHIP2 on whole body insulin sensitivity and insulin action in liver and muscle tissue in a die...
Cell migration is essential for various physiological and pathological processes. Polarization in motile cells requires the coordination of several key signaling molecules, including RhoA small GTPases and phosphoinositides. Although RhoA participates in a front-rear polarization in migrating cells, little is known about the functional interaction between RhoA and lipid turnover. We find here t...
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