共查询到20条相似文献,搜索用时 906 毫秒
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Verenice Paredes Jeong Soo Park Yongsu Jeong Jaeseung Yoon Kwanghee Baek 《Biotechnology letters》2013,35(7):987-993
The gradual loss of recombinant protein expression in CHO cell lines during prolonged subculture is a common issue, referred to as instability, which seriously affects the industrial production processes of therapeutic proteins. Loss of recombinant gene copies, due to the genetic instability of CHO cells, and epigenetic silencing of transgene sequences, are the main reported causes of production instability. To increase our understanding on the molecular mechanisms inherent to CHO cells involved in production instability, we explored the molecular features of stable and unstable antibody producing cell lines obtained without gene amplification, to exclude the genetic instability induced by the gene amplification process. The instability of recombinant antibody production during long-term culture was caused by a 48–53 % decrease in recombinant mRNA levels without significant loss of recombinant gene copies, but accompanied by a ~45 % decrease in histone H3 acetylation (H3ac). Thus, our results suggest a critical role of H3ac in the stability of recombinant protein production. 相似文献
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Jung-Sung Chung Jian-Kang Zhu Ray A. Bressan Paul M. Hasegawa Huazhong Shi 《The Plant journal : for cell and molecular biology》2008,53(3):554-565
Salt Overly Sensitive 1 (SOS1), a plasma membrane Na+ /H+ antiporter in Arabidopsis, is a salt tolerance determinant crucial for the maintenance of ion homeostasis in saline stress conditions. SOS1 mRNA is unstable at normal growth conditions, but its stability is substantially increased under salt stress and other ionic and dehydration stresses. In addition, H2 O2 treatment increases the stability of SOS1 mRNA. SOS1 mRNA is inherently unstable and rapidly degraded with a half-life of approximately 10 min. Rapid decay of SOS1 mRNA requires new protein synthesis. Stress-induced SOS1 mRNA stability is mediated by reactive oxygen species (ROS). NADPH oxidase is also involved in the upregulation of SOS1 mRNA stability, presumably through the control of extracellular ROS production. The cis -element required for SOS1 mRNA instability resides in the 500-bp region within the 2.2 kb at the 3' end of the SOS1 mRNA. Furthermore, mutations in the SOS1 gene render sos1 mutants more tolerant to paraquat, a non-selective herbicide causing oxidative stress, indicating that SOS1 plays negative roles in tolerance of oxidative stress. A hypothetical model for the signaling pathway involving SOS1-mediated pH changes, NADPH oxidase activation, apoplastic ROS production and downstream signaling transduction is proposed, and the biological significance of ROS-mediated induction of SOS1 mRNA stability is discussed. 相似文献
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Bourcier C Griseri P Grépin R Bertolotto C Mazure N Pagès G 《American journal of physiology. Cell physiology》2011,301(3):C609-C618
Most melanoma cells are characterized by the V600E mutation in B-Raf kinase. This mutation leads to increased expression of interleukin (CXCL8), which plays a key role in cell growth and angiogenesis. Thus CXCL8 appears to be an interesting therapeutic target. Hence, we performed vaccination of mice with GST-CXCL8, which results in a reduced incidence of syngenic B16 melanoma cell xenograft tumors. We next addressed the molecular mechanisms responsible for aberrant CXCL8 expression in melanoma. The CXCL8 mRNA contains multiples AU-rich sequences (AREs) that modulate mRNA stability through the binding of tristetraprolin (TTP). Melanoma cell lines express very low TTP levels. We therefore hypothesized that the very low endogenous levels of TTP present in different melanoma cell lines might be responsible for the relative stability of CXCL8 mRNAs. We show that TTP is actively degraded by the proteasome and that extracellular-regulated kinase inhibition results in TTP accumulation. Conditional expression of TTP in A375 melanoma cells leads to CXCL8 mRNA destabilization via its 3' untranslated regions (3'-UTR), and TTP overexpression reduces its production. In contrast, downregulation of TTP by short hairpin RNA results in upregulation of CXCL8 mRNA. Maintaining high TTP levels in melanoma cells decreases cell proliferation and autophagy and induces apoptosis. Sorafenib, a therapeutic agent targeting Raf kinases, decreases CXCL8 expression in melanoma cells through reexpression of TTP. We conclude that loss of TTP represents a key event in the establishment of melanomas through constitutive expression of CXCL8, which constitutes a potent therapeutic target. 相似文献
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Satoshi Oguchi Hiroyuki Saito Masayoshi Tsukahara Haruhiko Tsumura 《Cytotechnology》2006,52(3):199-207
Controlling cell proliferation during cell culturing is an effective way to improve the production yield in mammalian cell
culture. We examined the effect of temperature shifts (TS) under pH control conditions in Chinese hamster ovary cells. When
we shifted the culture temperature from 37 °C to 31 °C before a stationary phase at pH 6.8 (TS/pH 6.8), cell viability remained
high, and the final human monoclonal antibody (hMab) concentration increased to 2.3 times that in the culture remaining at
37 °C. However, there were no significant effects on the cell viability or production yield with the same TS at pH 7.0 (TS/pH
7.0). The average specific hMab productivity and mRNA level of TS/pH 7.0 were the same as that of TS/pH 6.8. The control of
cell growth by the TS or the addition of rapamycin was effective in the maintenance of cell viability, but there was no significant
increase of the average specific hMab productivity in the culture where cell proliferation was controlled with rapamycin.
The hMab mRNA concentration decreased to 55%–65% at a 37 °C culture with the addition of actinomycin D. In contrast, actinomycin
D did not affect the mRNA level in the TS culture. This result suggested that the increase in the mRNA level in the TS condition
was caused by an increase in mRNA stability. In this study, we show that TS can produce two unrelated effects: a prolongation
of cell longevity and an improvement in mRNA stability. 相似文献
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Stability of protein production from recombinant mammalian cells 总被引:6,自引:0,他引:6
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Dimitrios Tsitsipatis Ioannis Grammatikakis Riley K Driscoll Xiaoling Yang Kotb Abdelmohsen Sophia C Harris Jen-Hao Yang Allison B Herman Ming-Wen Chang Rachel Munk Jennifer L Martindale Krystyna Mazan-Mamczarz Supriyo De Ashish Lal Myriam Gorospe 《Nucleic acids research》2021,49(3):1631
Mammalian circRNAs can influence different cellular processes by interacting with proteins and other nucleic acids. Here, we used ribonucleoprotein immunoprecipitation (RIP) analysis to identify systematically the circRNAs associated with the cancer-related protein AUF1. Among the circRNAs interacting with AUF1 in HeLa (human cervical carcinoma) cells, we focused on hsa_circ_0032434 (circPCNX), an abundant target of AUF1. Overexpression of circPCNX specifically interfered with the binding of AUF1 to p21 (CDKN1A) mRNA, thereby promoting p21 mRNA stability and elevating the production of p21, a major inhibitor of cell proliferation. Conversely, silencing circPCNX increased AUF1 binding to p21 mRNA, reducing p21 production and promoting cell division. Importantly, eliminating the AUF1-binding region of circPCNX abrogated the rise in p21 levels and rescued proliferation. Therefore, we propose that the interaction of circPCNX with AUF1 selectively prevents AUF1 binding to p21 mRNA, leading to enhanced p21 mRNA stability and p21 protein production, thereby suppressing cell growth. 相似文献
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Bradley S. Carter Jonathan S. Fletcher Robert C. Thompson 《Methods (San Diego, Calif.)》2010,52(4):322-331
The analysis of the spatial patterning of mRNA expression is critically important for assigning functional and physiological significance to a given gene product. Given the tens of thousands of mRNAs in the mammalian genome, a full assessment of individual gene functions would ideally be overlaid upon knowledge of the specific cell types expressing each mRNA. In situ hybridization approaches represent a molecular biological/histological method that can reveal cellular patterns of mRNA expression. Here, we present detailed procedures for the detection of specific mRNAs using radioactive RNA probes in tissue sections followed by autoradiographic detection. These methods allow for the specific and sensitive detection of spatial patterns of mRNA expression, thereby linking mRNA expression with cell type and function. Radioactive detection methods also facilitate semi-quantitative analyses of changes in mRNA gene expression. 相似文献
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Mandal D Srivastava A Mahlum E Desai D Maran A Yaszemski M Jalal SM Gitelis S Bertoni F Damron T Irwin R O'connor M Schwartz H Bolander ME Sarkar G 《Gene》2007,386(1-2):131-138
Deciphering the molecular basis of cancer is critical for developing novel diagnostic and therapeutic strategies. To better understand the early molecular events involving osteogenic sarcoma (OGS), we have initiated a program to identify potential tumor suppressor genes. Expression profiling of total RNA from ten normal bone cell lines and eleven OGS-derived cell lines by microarray showed 135-fold lower expression of FRZB/sFRP3 mRNA in OGS cells compared to bone cells; this down-regulation of Frzb/sFRP3 mRNA expression was found to be serum-independent. Subsequently, fourteen OGS biopsy specimens showed nine-fold down-regulation of Frzb/sFRP3 mRNA expression compared to expression in eight normal bone specimens as determined by microarray. FRZB /sFRP3 protein level was also found to be at a very low level in 4/4 OGS cell lines examined. Quantitation by RT-PCR indicated approximately 70% and approximately 90% loss of Frzb/sFRP3 mRNA expression in OGS biopsy specimens and OGS-derived cell lines respectively, compared to expression in bone (p<0.0001). Hybridization experiments of a cDNA microarray containing paired normal and tumor specimens from nineteen different organs did not show any significant difference in the level of Frzb/sFRP3 mRNA expression between the normal and the corresponding tumor tissues. Exogenous expression of FRZB/sFRP3 mRNA in two OGS-derived cell lines lacking endogenous expression of the mRNA produced abundant mRNA from the exogenous gene, eliminating degradation as a possibility for very low level of FRZB/sFRP3 mRNA in OGS specimens. Results from PCR-based experiments suggest that the FRZB/sFRP3 gene is not deleted in OGS cell lines, however, karyotyping shows gross abnormalities involving chromosome 2 (location of the FRZB gene) in five of twelve OGS-derived cell lines. Together, these data suggest a tumor-suppressive potential for FRZB/sFRP3 in OGS. 相似文献
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Nicotinic acid (niacin) has been used clinically to manage dyslipidemia for many years. The molecular target of nicotinic
acid was unknown until the recent revelation of human G-coupled receptor HM74a as the high affinity receptor for nicotinic
acid. In searching for a cell line expressing endogenous human HM74a receptor, we have identified that the A431 cell line,
a human epidermoid cell line, expresses a high level of HM74a receptor. An HM74a-specific real time PCR probe set was designed
and the mRNA levels of HM74a in A431 and 32 other cultured cell lines were measured quantitatively. When the mRNA expression
of HM74a in A431 cells was compared to that in human primary preadipocytes, adipocytes and adipose tissue, we found that the
level in A431 was about 10- fold higher than that in adipocytes and adipose tissue. The ratio of HM74a:HM74 mRNA was measured
quantitatively and it was determined to be 3:2 in A431 cells. The function of the HM74a receptor in A431 cells was evaluated
for its ability to inhibit forskolin-induced cAMP production. Pertussis toxin treatment abolished the inhibition. Our data
suggest that the A431 cell line may serve as a cellular model for further investigation of niacin/HM74a-mediated signal transduction
in modulating metabolism. A431 cell line may also provide a valuable cell model to study prostaglandin production upon HM74a
activation to improve our understanding of niacin/HM74a-mediated skin flushing.
The first two author contributed equally. 相似文献
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mRNA疫苗的开发及临床研究进展 总被引:1,自引:0,他引:1
随着mRNA稳定性和安全高效的递送系统的研究日渐成熟,近年来,mRNA疫苗在肿瘤个体化疫苗中取得了较大进展,因其生产工艺简单、在细胞内表达抗原、安全性优于DNA疫苗等特点,是一种很有前途的新型疫苗。为了解全球mRNA疫苗的开发与研究现状,在此重点对mRNA疫苗的分子设计、递送系统、临床研究现状进行了分析和综述,为后续mRNA疫苗的开发和研究提供参考依据。 相似文献