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Roles of periostin in symptom manifestation and airway remodeling in a murine model of allergic rhinitis.

Hur DG, Khalmuratova R, Ahn SK, Ha YS, Min YG - Allergy Asthma Immunol Res (2012)

Bottom Line: No differences in the expression of MMP-2 or TIMP-1 were found in the knockout group.However, after a month of allergen challenge, type I collagen in the nasal tissue was lower in the knockout group than in the control group.The number of eosinophils and the symptom score were also lower in the knockout group.

View Article: PubMed Central - PubMed

Affiliation: Department of Otorhinolaryngology, School of Medicine, Gyeongsang National University, Jinju, Korea.

ABSTRACT

Purpose: Periostin was originally identified as a secreted factor during screening of a mouse osteoblastic library. In a recent study, periostin was found to directly regulate eosinophil accumulation in allergic mucosal inflammation. Chronic eosinophilic inflammation is related to the development of remodeling. The present study examined the expression of periostin and evaluated its role in the inflammatory process and remodeling associated with allergic rhinitis.

Methods: A murine model of allergic rhinitis was established in periostin knockout mice. We analyzed the expression of periostin, manifestation of nasal symptoms, eosinophilic inflammation, and subepithelial fibrosis as well as the expression of MMP-2, TIMP-1, and type 1 collagen in nasal tissue.

Results: Periostin was mainly distributed in the subepithelial tissue of the nasal mucosa. The subepithelial tissue was thinner in the knockout group than in the control group. No differences in the expression of MMP-2 or TIMP-1 were found in the knockout group. However, after a month of allergen challenge, type I collagen in the nasal tissue was lower in the knockout group than in the control group. The number of eosinophils and the symptom score were also lower in the knockout group.

Conclusions: Periostin is expressed in nasal tissues of murine models of allergic rhinitis. Periostin deficiency may affect the remodeling of nasal tissue with reduced subepithelial fibrosis, and lead to less eosinophilic inflammation.

No MeSH data available.


Related in: MedlinePlus

Periostin levels in serum. Serum periostin levels were not significantly different in the PBS or OVA groups over time. After 19 days, 1 month, and 3 months of allergen challenge, the PBS and OVA groups showed similar serum periostin levels. Serum periostin was not found in the KO group. Data are expressed as mean±SE.PBS, phosphate buffered saline; OVA, ovalbumin; KO, knockout.
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Figure 3: Periostin levels in serum. Serum periostin levels were not significantly different in the PBS or OVA groups over time. After 19 days, 1 month, and 3 months of allergen challenge, the PBS and OVA groups showed similar serum periostin levels. Serum periostin was not found in the KO group. Data are expressed as mean±SE.PBS, phosphate buffered saline; OVA, ovalbumin; KO, knockout.

Mentions: Serum periostin was found in the PBS and OVA groups. However, serum periostin levels were not significantly different in the PBS or OVA groups over time. None was found in the KO group, and levels were constant in all groups despite the presence of a nasal allergic response (Fig. 3).


Roles of periostin in symptom manifestation and airway remodeling in a murine model of allergic rhinitis.

Hur DG, Khalmuratova R, Ahn SK, Ha YS, Min YG - Allergy Asthma Immunol Res (2012)

Periostin levels in serum. Serum periostin levels were not significantly different in the PBS or OVA groups over time. After 19 days, 1 month, and 3 months of allergen challenge, the PBS and OVA groups showed similar serum periostin levels. Serum periostin was not found in the KO group. Data are expressed as mean±SE.PBS, phosphate buffered saline; OVA, ovalbumin; KO, knockout.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3378929&req=5

Figure 3: Periostin levels in serum. Serum periostin levels were not significantly different in the PBS or OVA groups over time. After 19 days, 1 month, and 3 months of allergen challenge, the PBS and OVA groups showed similar serum periostin levels. Serum periostin was not found in the KO group. Data are expressed as mean±SE.PBS, phosphate buffered saline; OVA, ovalbumin; KO, knockout.
Mentions: Serum periostin was found in the PBS and OVA groups. However, serum periostin levels were not significantly different in the PBS or OVA groups over time. None was found in the KO group, and levels were constant in all groups despite the presence of a nasal allergic response (Fig. 3).

Bottom Line: No differences in the expression of MMP-2 or TIMP-1 were found in the knockout group.However, after a month of allergen challenge, type I collagen in the nasal tissue was lower in the knockout group than in the control group.The number of eosinophils and the symptom score were also lower in the knockout group.

View Article: PubMed Central - PubMed

Affiliation: Department of Otorhinolaryngology, School of Medicine, Gyeongsang National University, Jinju, Korea.

ABSTRACT

Purpose: Periostin was originally identified as a secreted factor during screening of a mouse osteoblastic library. In a recent study, periostin was found to directly regulate eosinophil accumulation in allergic mucosal inflammation. Chronic eosinophilic inflammation is related to the development of remodeling. The present study examined the expression of periostin and evaluated its role in the inflammatory process and remodeling associated with allergic rhinitis.

Methods: A murine model of allergic rhinitis was established in periostin knockout mice. We analyzed the expression of periostin, manifestation of nasal symptoms, eosinophilic inflammation, and subepithelial fibrosis as well as the expression of MMP-2, TIMP-1, and type 1 collagen in nasal tissue.

Results: Periostin was mainly distributed in the subepithelial tissue of the nasal mucosa. The subepithelial tissue was thinner in the knockout group than in the control group. No differences in the expression of MMP-2 or TIMP-1 were found in the knockout group. However, after a month of allergen challenge, type I collagen in the nasal tissue was lower in the knockout group than in the control group. The number of eosinophils and the symptom score were also lower in the knockout group.

Conclusions: Periostin is expressed in nasal tissues of murine models of allergic rhinitis. Periostin deficiency may affect the remodeling of nasal tissue with reduced subepithelial fibrosis, and lead to less eosinophilic inflammation.

No MeSH data available.


Related in: MedlinePlus