scholarly journals Distribution of phospholipase C isozymes in normal human lung tissue and their immunohistochemical localization

1996 ◽  
Vol 11 (4) ◽  
pp. 305 ◽  
Author(s):  
Sung Chul Hwang ◽  
Kwang Hwa Park ◽  
Mahn Joon Ha ◽  
In Sook Noh ◽  
Tae Byung Park ◽  
...  
2007 ◽  
Vol 22 (3) ◽  
pp. 226-231 ◽  
Author(s):  
L. Speranza ◽  
M.A. De Lutiis ◽  
Y.B. Shaik ◽  
M. Felaco ◽  
A. Patruno ◽  
...  

1982 ◽  
Vol 63 (2) ◽  
pp. 219-221 ◽  
Author(s):  
V. Y. Lee ◽  
J. Margaret Hughes ◽  
J. P. Seale ◽  
Diana M. Temple

1. Macroscopically normal human lung tissue was obtained from operative specimens removed for lung cancer and challenged with antigen or calcium ionophore. The release of histamine and slow-reacting substances was measured by fluorimetric and bioassay techniques respectively. 2. Benoxaprofen, a drug with inhibitory effects on the lipoxygenase and cyclo-oxygenase pathways, caused a dose-related reduction of release of slow-reacting substances without affecting histamine release. 3. These results with human lung tissue in vitro suggest that benoxaprofen may be used to investigate the role of slow-reacting substances in experimental and clinical asthma.


Oncogene ◽  
2007 ◽  
Vol 27 (11) ◽  
pp. 1650-1656 ◽  
Author(s):  
F S Falvella ◽  
M Spinola ◽  
C Pignatiello ◽  
S Noci ◽  
B Conti ◽  
...  

2014 ◽  
Author(s):  
Jianxin Shi ◽  
Crystal Marconett ◽  
Jubao Duan ◽  
Paula Hyland ◽  
Peng Li ◽  
...  

2004 ◽  
pp. 151-154 ◽  
Author(s):  
T Nohira ◽  
K Nagao ◽  
K Kameyama ◽  
H Nakai ◽  
N Fukumine ◽  
...  

OBJECTIVE: Adipocytes secrete a number of molecules such as tumor necrosis factor-alpha, leptin and free fatty acids that can influence the ability of the body to metabolize glucose. Recently, a novel 12.5 kDa cysteine-rich protein, termed resistin, was shown to be secreted by adipocytes. Resistin expression was markedly induced during the conversion of 3T3-L1 cells to mature adipocytes. Expression of resistin has been studied in human, mouse and rat; however, sequence information about an alternative splicing variant (ASV) of resistin mRNA has not been reported. In the present study, we investigated the occurrence of a novel ASV of the resistin gene in human normal tissues. DESIGN AND METHODS: We identified a novel ASV of resistin mRNA in human lung tissue by RT-PCR analysis in human lung tissue. We then investigated a novel ASV of resistin mRNA by real-time PCR analysis in 26 different types of normal human tissues. RESULTS AND CONCLUSIONS: We identified a novel deletion variant of the resistin transcript in the normal human tissues. The deleted transcript of resistin was characterized by an in-frame deletion of 78 bp, corresponding to the complete loss of exon 2 (resistin delta2 ASV). Thus, resistin delta2 ASV causes protein truncation. Our results provide the basis for more detailed studies on the regulation of resistin activity, and should assist in the development of clinical trials with resistin for the central regulation of adipogenesis and adipocyte metabolism.


1994 ◽  
Vol 266 (6) ◽  
pp. L722-L727 ◽  
Author(s):  
W. R. Tracey ◽  
C. Xue ◽  
V. Klinghofer ◽  
J. Barlow ◽  
J. S. Pollock ◽  
...  

Type II (inducible) nitric oxide synthase (NOS) may play an important role in pulmonary pathophysiology, yet it remains controversial whether human tissues are capable of expressing this protein. Therefore, a polyclonal antibody (8196) was raised against type II NOS from induced RAW 264.7 macrophages and used to investigate the expression of this enzyme in human lung tissue. Anti-type II NOS antibody did not cross-react with either neuronal (type I) or endothelial (type III) constitutive NOS, whereas a 130-kDa protein was detected in cytosol from induced macrophages or liver removed from lipopolysaccharide (25 mg/kg)-treated rats. Cells or tissues that lacked NOS activity did not express immunoreactive proteins. Similarly, in grossly normal human lung tissue, no immunoreactivity was detected with the anti-type II NOS antibody. In contrast, strong immunoreactivity was detected in alveolar macrophages present in lung tissue from a patient with bronchiectasis and acute bronchopneumonia. These data demonstrate that human alveolar macrophages are able to express type II NOS and support a role for this enzyme in pulmonary inflammatory pathophysiology.


2014 ◽  
Vol 5 (1) ◽  
Author(s):  
Jianxin Shi ◽  
Crystal N. Marconett ◽  
Jubao Duan ◽  
Paula L. Hyland ◽  
Peng Li ◽  
...  

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