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2354 citation(s) found for "Xu, Long".

NF-κBcis-Acting Motifs of the Human Immunodeficiency Virus (HIV) Long Terminal Repeat Regulate HIV Transcription in Human Macrophages
Asin, Susana , Bren, Gary D., Carmona, Eva M. , Solan, Nancie J., Payá, Carlos V., Carmona, Eva M

Mayo Clinic

Journal of Virology | July 27, 2002 | Volume: 75 | Issue: 23 | Pages: 11408-11416

10.1128/jvi.75.23.11408-11416.2001 | PMID 11689622 Get It

ABSTRACTThe role of NF-κB in the reactivation of human immunodeficiency virus (HIV) from latency in CD4 T lymphocytes is well documented. However, its role in driving HIV transcription in human macrophages, which contain a constitutive nuclear pool of NF-κB, is less well understood. In this study we have investigated the role that the constitutive pool of NF-κB and the NF-κBcis-acting motifs of the HIV long terminal repeat (LTR) play in regulating HIV transcription in human monocytic cells and primary macrophages. Inhibition of the constitutive nuclear pool of NF-κB (RelA and RelB) in the promonocytic U937 cell line using dominant-negative IκBα significantly decreases HIV replication. Moreover, it is demonstrated that in the differentiated monocytic cell line THP1, which contains a constitutive nuclear pool of NF-κB (RelB),an HIV provirus containing mutations of the κBcis-acting sites in the LTR is transcriptionally impaired. Reduction of the constitutive pool of NF-κB in human macrophages by an adenovirus vector expressing a dominant-negative IκBα also reduces HIV transcription. Lastly, mutation of the NF-κBcis-acting sites in the LTR of an R5 HIV provirus completely abrogates the first cycle of HIV transcription. These studies indicate that thecis-acting NF-κB motifs of the HIV LTR are critical in initiating HIV transcription in human macrophages and suggest that the constitutive nuclear pool of NF-κB is important in regulating HIV transcription in these cells.
Long-Term Fracture Risk among Infertile Women: A Population-Based Cohort Study
Melton, L. Joseph, Hesdorffer, Dale C. , Malkasian, George D., Atkinson, Elizabeth J. , Brinton, Louise A. , O’Fallon, W. Michael

Mayo Clinic

Journal of Women's Health & Gender-Based Medicine | July 26, 2002 | Volume: 10 | Issue: 3 | Pages: 289-297

10.1089/152460901300140040 | PMID 11389789 Get It

An optical spin micromotor
Luo, Zong-Ping , Sun, Yu-Long, An, Kai‐Nan

Mayo Clinic

Applied Physics Letters | July 26, 2002 | Volume: 76 | Issue: 13 | Pages: 1779-1781

10.1063/1.126165 Get It

An optical spin micromotor operated by optical tweezers, described in the present study, converts radiant energy directly to mechanical energy. This conversion is of great practical and fundamental interest. The optical spin micromotor consists of a two-bead linkage. The large bead (2.0 μm in diameter) is trapped by the optical tweezers and rotates around the laser beam axis. The small bead (0.94 μm in diameter) is partially coated with gold/palladium for generating the spin torque through the change of momentum from gradient radiation pressure of the same laser applied on the coated small bead. With a laser power of 29 mW at the sample plane, the spin speed averaged 158.8±155.5 rpm (mean±standard deviation) and the torque was estimated as 101.9±99.8 pN nm. This optical spin micromotor will be useful in (1) providing a fundamental step toward developing optical-operated mechanical devices, (2) twisting macromolecules, and (3) generating vortex and shear force in medium at nanoscale.
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation
Rinaldo, Piero, Rhead, William J., Tian, Liqun, Millington, David S., Vockley, Jerry , Hamm, Doug A., Brix, Amy E., Lindsey, J. Russell, Pinkert, Carl A. , O’Brien, William E., Kurtz, David M. , Wood, Philip A.

Mayo Clinic

Proceedings of the National Academy of Sciences | July 26, 2002 | Volume: 95 | Issue: 26 | Pages: 15592-15597

10.1073/pnas.95.26.15592 | PMID 9861014 Get It

Abnormalities of fatty acid metabolism are recognized to play a significant role in human disease, but the mechanisms remain poorly understood. Long-chain acyl-CoA dehydrogenase (LCAD) catalyzes the initial step in mitochondrial fatty acid oxidation (FAO). We produced a mouse model of LCAD deficiency with severely impaired FAO. Matings between LCAD +/− mice yielded an abnormally low number of LCAD +/− and −/− offspring, indicating frequent gestational loss. LCAD −/− mice that reached birth appeared normal, but had severely reduced fasting tolerance with hepatic and cardiac lipidosis, hypoglycemia, elevated serum free fatty acids, and nonketotic dicarboxylic aciduria. Approximately 10% of adult LCAD −/− males developed cardiomyopathy, and sudden death was observed in 4 of 75 LCAD −/− mice. These results demonstrate the crucial roles of mitochondrial FAO and LCAD in vivo .