Expression of TREM-1 mRNA in acute pancreatitis.

World J Gastroenterol

Department of Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, Hubei Province, China.

Published: September 2004

AI Article Synopsis

  • The study investigates the expression levels of TREM-1 mRNA in patients with acute pancreatitis (AP) compared to healthy individuals, revealing higher levels in both mild and severe cases.
  • Significant differences in TREM-1 mRNA expression were observed among mild acute pancreatitis (MAP), severe acute pancreatitis (SAP), and healthy controls, indicating a correlation with disease severity.
  • The expression of TREM-1 mRNA also varied at different treatment stages, suggesting it may play a critical role in the progression of acute pancreatitis.

Article Abstract

Aim: To explore the expression of triggering receptor expressed on myeloid cells (TREM-1) mRNA in acute pancreatitis (AP).

Methods: Using the reverse transcription polymerase chain reaction (RT-PCR), we examined the expression of TREM-1 mRNA in 10 cases of mild acute pancreatitis (MAP), 8 cases of severe acute pancreatitis (SAP), and 10 cases of healthy control subjects. And we also examined the expression of TREM-1 mRNA in 14 cases of AP (including 10 MAP and 4 SAP) before treatment, after successful therapy and clinically cured.

Results: The expression of TREM-1 mRNA in the groups of MAP, SAP patients and healthy control subjects was 0.771+/-0.274, 1.092+/-0.331 and 0.459+/-0.175, respectively; there was a significant difference among the three groups (P<0.05). And there was also a significant difference between the AP patients (0.914+/-0.341) and healthy control subjects (0.459+/-0.175) (P<0.05). Moreover, in the 14 cases of AP, before treatment, after successful therapy and clinically cured, the expression of TREM-1 mRNA was 0.905+/-0.226, 0.739+/-0.169 and 0.633+/-0.140, respectively, and there was a significant difference among the three stages (P<0.05).

Conclusion: The expression of TREM-1 mRNA in the patients with AP increases obviously, and correlates with the degree of AP. Furthermore, the expression of TREM-1 mRNA is distinctly different at the different stages of AP. It indicates TREM-1 may play an important role in the occurrence and development of AP.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572206PMC
http://dx.doi.org/10.3748/wjg.v10.i18.2744DOI Listing

Publication Analysis

Top Keywords

trem-1 mrna
20
expression trem-1
16
acute pancreatitis
16
mrna acute
8
examined expression
8
mrna cases
8
healthy control
8
control subjects
8
map sap
8
expression
5

Similar Publications

Soluble epoxide hydrolase inhibition impairs triggering receptor expressed on myeloid cells-1 in periodontal tissue.

J Periodontal Res

September 2024

Laboratory of Neuroimmune Interface of Pain Research, Faculdade São Leopoldo Mandic, Instituto de Pesquisa São Leopoldo Mandic, Campinas, Brazil.

Aims: Periodontitis is a prevalent inflammatory disorder affecting the oral cavity, driven by dysbiotic oral biofilm and host immune response interactions. While the major clinical focus of periodontitis treatment is currently controlling oral biofilm, understanding the immune response is crucial to prevent disease progression. Soluble epoxide hydrolase (sEH) inhibition has shown promise in preventing alveolar bone resorption.

View Article and Find Full Text PDF

N6-methyladenosine-mediated overexpression of TREM-1 is associated with periodontal disease.

Odontology

September 2024

Molecular Biology Lab, Centre for Cellular and Molecular Research, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, 600077, India.

Periodontitis, a prevalent inflammatory disease, involves the destruction of tooth-supporting tissues. N6-methyladenosine (m6A) is a type of post-transcriptional modification that significantly influences gene and protein expression. It is involved in the regulation of various diseases, including those with an inflammatory component.

View Article and Find Full Text PDF

Increased serum levels of high-mobility group box 1 protein and the location characteristics in the patients of intracranial aneurysms.

Brain Res

April 2024

Department of Neurosurgery, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei Province, China; Hubei Key Laboratory of Embryonic Stem Cell Research, Taihe Hospital, Hubei University of Medicine, China. Electronic address:

Objective: Inflammation-related factors play a crucial role in intracranial aneurysms (IA) initiation, progression, and rupture. High mobility group box 1 (HMGB-1) serves as an alarm to drive the pathogenesis of the inflammatory disease. This study aimed to evaluate the role of HMGB-1 in IA and explore the correlation with other inflammatory-related factors.

View Article and Find Full Text PDF
Article Synopsis
  • Researchers are investigating the role of TREM-1 in myeloid dendritic cells (mDCs) and its therapeutic potential in systemic lupus erythematosus (SLE), a complex autoimmune disease influenced by epigenetic mechanisms and non-coding RNAs.
  • * The study utilized bioinformatics to analyze gene expression differences between SLE patients and healthy individuals, identifying TREM-1 as a key gene related to disease progression and a potential biomarker in serum.
  • * Findings showed that activating TREM-1 led to increased mDC activation and inflammation, while targeting it with the miRNA miR-150-5p could potentially mitigate SLE symptoms in lupus mice models.*
View Article and Find Full Text PDF

Introduction: Exposure to high-dose ionizing radiation causes tissue injury, infections and even death due to immune dysfunction. The triggering receptor expressed on myeloid cells-1 (TREM-1) has been demonstrated to critically amplify and dysregulate immune responses. However, the role of TREM-1 in radiation injury remains unknown.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!