Johnson Controls, Inc. articles
Abstract
Reactive astrocytes are associated with every form of neurological injury. Despite their ubiquity, the molecular mechanisms controlling their production and diverse functions remain poorly defined. Because many features of astrocyte development are recapitulated in reactive astrocytes, we investigated the role of nuclear factor I-A (NFIA), a key transcriptional regulator of astrocyte development whose contributions to reactive astrocytes remain undefined. Her
Dylan Laug,;Teng-Wei Huang;Debosmita Sardar;Joshua Ortiz-Guzman;Jeffrey C. Carlson;Benjamin R. Arenkiel;Chay T. Kuo;Carrie A. Mohila;Stacey M. Glasgow
Abstract
Electronic nicotine delivery systems (ENDS) or e-cigarettes have emerged as a popular recreational tool among adolescents and adults. Although the use of ENDS is often promoted as a safer alternative to conventional cigarettes, few comprehensive studies have assessed the long-term effects of vaporized nicotine and its associated solvents, propylene glycol (PG) and vegetable glycerin (VG). Here, we show that compared with smoke exposure, mice receiving ENDS va
Matthew C. Madison;Cameron T. Landers;Bon-Hee Gu;Cheng-Yen Chang;Hui-Ying Tung;Ran You;Monica J. Hong;Nima Baghaei;Li-Zhen Song;Paul Porter;Nagireddy Putluri;Nagireddy Putluri;Ramiro Salas
Abstract
Fibronectin in the vascular wall promotes inflammatory activation of the endothelium during vascular remodeling and atherosclerosis. These effects are mediated in part by fibronectin binding to integrin α5, which recruits and activates phosphodiesterase 4D5 (PDE4D5) by inducing its dephosphorylation on an inhibitory site, S651. Active PDE then hydrolyzes antiinflammatory cAMP to facilitate inflammatory signaling. To test this model in vivo, we mutated t
Sanguk Yun;Rui Hu;Melanie E. Schwaemmle,;Alexander N. Scherer;Zhenwu Zhuang;Anthony J. Koleske,;David C. Pallas;Martin A. Schwartz
Abstract
We previously generated 32 rotavirus-specific (RV-specific) recombinant monoclonal antibodies (mAbs) derived from B cells isolated from human intestinal resections. Twenty-four of these mAbs were specific for the VP8* fragment of RV VP4, and most (20 of 24) were non-neutralizing when tested in the conventional MA104 cell–based assay. We reexamined the ability of these mAbs to neutralize RVs in human intestinal epithelial cells including ileal enteroids
Ningguo Feng;Liya Hu;Siyuan Ding;Mrinmoy Sanyal;Boyang Zhao;Banumathi Sankaran;Sasirekha Ramani;Monica McNeal;Linda L. Yasukawa;Yanhua Song;Harry B. Greenberg
Idiopathic pulmonary fibrosis (IPF) is a chronic and fatal lung disease. A maladaptive epithelium due to chronic injury is a prominent feature and contributor to pathogenic cellular communication in IPF. Recent data highlight the concept of a “reprogrammed” lung epithelium as critical in the development of lung fibrosis. Extracellular vesicles (EVs) are potent mediators of cellular crosstalk, and recent evidence supports their role in lung pathologies, such as IPF. Here, we demons
Tanyalak Parimon;Changfu Yao;David M. Habiel;Lingyin Ge;Stephanie A. Bora;Rena Brauer;Christopher M. Evans;Ting Xie;Felix Alonso-Valenteen
A population of NK cells expressing the activating receptor NKG2C and the maturation marker CD57 expands in response to human CMV (HCMV) infection. CD3–CD56dimCD57+NKG2C+ NK cells are similar to CD8+ memory T cells with rapid and robust effector function upon restimulation, persistence, and epigenetic remodeling of the IFNG locus. Chronic antigen stimulation drives CD8+ memory T cell proliferation, while also inducing gen
Aimee Merino;Bin Zhang;Philip Dougherty;Xianghua Luo;Jinhua Wang;Bruce R. Blazar;Jeffrey S. Miller;Frank Cichocki
Deep brain stimulation (DBS) is used to treat multiple neuropsychiatric disorders, including Parkinson’s disease (PD). Despite widespread clinical use, its therapeutic mechanisms are unknown. Here, we developed a mouse model of subthalamic nucleus (STN) DBS for PD, to permit investigation using cell type–specific tools available in mice. We found that electrical STN DBS relieved bradykinesia, as measured by movement velocity. In addition, our model recapitulated several hallmarks
Jonathan S. Schor;Alexandra B. Nelson
Abstract
Serine-rich splicing factor 3 (SRSF3) plays a critical role in liver function and its loss promotes chronic liver damage and regeneration. As a consequence, genetic deletion of SRSF3 in hepatocytes caused progressive liver disease and ultimately led to hepatocellular carcinoma. Here we show that SRSF3 is decreased in human liver samples with nonalcoholic fatty liver disease (NAFLD), nonalcoholic steatohepatitis (NASH), or cirrhosis that was associated with al
Deepak Kumar;Manasi Das;Consuelo Sauceda;Lesley G. Ellies,
