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Published on: October 2, 2017
Olfactomedin 4 expression and functions in innate immunity, inflammation, and cancer
Wenli Liu1, Griffin P Rodgers2
1Molecular and Clinical Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bldg. 10, Room 9N119, 9000 Rockville Pike, Bethesda, MD, 20892, USA.
Abstract:
Olfactomedin 4 (OLFM4) is an olfactomedin domain-containing glycoprotein. Multiple signaling pathways and factors, including NF-κB, Wnt, Notch, PU.1, retinoic acids, estrogen receptor, and miR-486, regulate its expression. OLFM4 interacts with several other proteins, such as gene associated with retinoic-interferon-induced mortality 19 (GRIM-19), cadherins, lectins, nucleotide oligomerization domain-1 (NOD1) and nucleotide oligomerization domain-2 (NOD2), and cathepsins C and D, known to regulate important cellular functions. Recent investigations using Olfm4-deficient mouse models have provided important clues about its in vivo biological functions. Olfm4 inhibited Helicobacter pylori-induced NF-κB pathway activity and inflammation and facilitated H. pylori colonization in the mouse stomach. Olfm4-deficient mice exhibited enhanced immunity against Escherichia coli and Staphylococcus aureus infection. Olfm4 deletion in a chronic granulomatous disease mouse model rescued them from S. aureus infection. Olfm4 deletion in mice treated with azoxymethane/dextran sodium sulfate led to robust intestinal inflammation and intestinal crypt hyperplasia. Olfm4 deletion in Apc (Min/+) mice promoted intestinal polyp formation as well as adenocarcinoma development in the distal colon. Further, Olfm4-deficient mice spontaneously developed prostatic epithelial lesions as they age. OLFM4 expression is correlated with cancer differentiation, stage, metastasis, and prognosis in a variety of cancers, suggesting its potential clinical value as an early-stage cancer marker or a therapeutic target. Collectively, these data suggest that OLFM4 plays important roles in innate immunity against bacterial infection, gastrointestinal inflammation, and cancer. In this review, we have summarized OLFM4's initial characterization, expression, regulation, protein interactions, and biological functions.
Insights
Olfactomedin 4 (OLFM4) protein impacts immunity and inflammation. Its absence in mice worsened gut inflammation and cancer but improved defense against certain bacterial infections, highlighting its complex roles.
Area of Science:
- Molecular Biology
- Immunology
- Oncology
Background:
- Olfactomedin 4 (OLFM4) is a glycoprotein regulated by multiple signaling pathways.
- OLFM4 interacts with various proteins involved in cellular functions.
- Its in vivo functions are increasingly understood through Olfm4-deficient mouse models.
Purpose of the Study:
- To review the characterization, expression, regulation, interactions, and biological functions of OLFM4.
- To elucidate OLFM4's roles in innate immunity, gastrointestinal inflammation, and cancer.
Main Methods:
- Analysis of Olfm4-deficient mouse models to study in vivo functions.
- Review of existing literature on OLFM4's molecular interactions and regulatory pathways.
- Correlation analysis of OLFM4 expression with cancer characteristics.
Main Results:
- Olfm4 deficiency enhanced immunity against Escherichia coli and Staphylococcus aureus but facilitated Helicobacter pylori colonization.
- Absence of Olfm4 led to severe intestinal inflammation and promoted tumor development in mouse models.
- OLFM4 expression correlates with cancer differentiation, stage, metastasis, and prognosis.
Conclusions:
- OLFM4 plays a critical role in innate immunity against bacterial infections.
- OLFM4 is implicated in regulating gastrointestinal inflammation and cancer progression.
- OLFM4 holds potential as an early-stage cancer biomarker and therapeutic target.
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