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- Publisher Website: 10.1111/j.1600-0765.2005.00827.x
- Scopus: eid_2-s2.0-27944437531
- PMID: 16302926
- WOS: WOS:000232893600008
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Article: Expression of human β-defensin-3 in gingival epithelia
Title | Expression of human β-defensin-3 in gingival epithelia |
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Authors | |
Keywords | Gingival epithelia Human β-defensin-3 Immunohistochemistry in situ hybridization |
Issue Date | 2005 |
Publisher | Wiley-Blackwell Publishing, Inc.. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=0022-3484&site=1 |
Citation | Journal Of Periodontal Research, 2005, v. 40 n. 6, p. 474-481 How to Cite? |
Abstract | Objective: This study aimed to investigate the expression patterns of the newly discovered human β-defensin-3 (hBD-3) in human gingiva. Background: Human β-defensins (hBDs) are a group of small, broad-spectrum, cationic antimicrobial peptides. Our recent study showed that the expression levels of hBD-1 and 2 peptides were associated with periodontal conditions. Methods: A total of 49 gingival biopsies were collected, including 33 samples from 21 patients with chronic periodontitis and 16 samples from 16 periodontally healthy subjects. The expression of hBD-3 was detected by immunohistochemistry and in situ hybridization. Double staining was undertaken to identify hBD-3 peptide-positive cells, using CD-1a and cytokeratin 20 as markers for Langerhans cells and Merkel cells, respectively. Results: hBD-3 peptide was detected in 88% of the samples, which was confined to the gingival epithelia. In healthy control subjects, hBD-3 peptide was more frequently detected in the basal layer as compared to the patients (53% vs. 18%, p < 0.05). In patients, hBD-3 expression extended from the basal layer to the spinous layers (82%), in which hBD-3 was confined to the basal and deep spinous layers in clinically healthy tissues from patients, whereas it extended to the superficial spinous layers in pocket tissues from patients (0% vs. 50%, p < 0.05). In both groups, hBD-3 peptide was expressed not only in gingival keratinocytes, but also in Langerhans cells and Merkel cells. hBD-3 transcripts were detected in 90% of the samples and they were confined to the basal and/or suprabasal layers of gingival epithelia. Conclusions: This study shows that hBD-3 is frequently expressed in gingival epithelia. The appropriate expression of hBD-3 peptide may contribute to the maintenance of periodontal homeostasis, possibly through its antimicrobial effect and promotion of adaptive immune responses. © Blackwell Munksgaard 2005. |
Persistent Identifier | http://hdl.handle.net/10722/154371 |
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 0.895 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lu, Q | en_US |
dc.contributor.author | Samaranayake, LP | en_US |
dc.contributor.author | Darveau, RP | en_US |
dc.contributor.author | Jin, L | en_US |
dc.date.accessioned | 2012-08-08T08:24:56Z | - |
dc.date.available | 2012-08-08T08:24:56Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.citation | Journal Of Periodontal Research, 2005, v. 40 n. 6, p. 474-481 | en_US |
dc.identifier.issn | 0022-3484 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/154371 | - |
dc.description.abstract | Objective: This study aimed to investigate the expression patterns of the newly discovered human β-defensin-3 (hBD-3) in human gingiva. Background: Human β-defensins (hBDs) are a group of small, broad-spectrum, cationic antimicrobial peptides. Our recent study showed that the expression levels of hBD-1 and 2 peptides were associated with periodontal conditions. Methods: A total of 49 gingival biopsies were collected, including 33 samples from 21 patients with chronic periodontitis and 16 samples from 16 periodontally healthy subjects. The expression of hBD-3 was detected by immunohistochemistry and in situ hybridization. Double staining was undertaken to identify hBD-3 peptide-positive cells, using CD-1a and cytokeratin 20 as markers for Langerhans cells and Merkel cells, respectively. Results: hBD-3 peptide was detected in 88% of the samples, which was confined to the gingival epithelia. In healthy control subjects, hBD-3 peptide was more frequently detected in the basal layer as compared to the patients (53% vs. 18%, p < 0.05). In patients, hBD-3 expression extended from the basal layer to the spinous layers (82%), in which hBD-3 was confined to the basal and deep spinous layers in clinically healthy tissues from patients, whereas it extended to the superficial spinous layers in pocket tissues from patients (0% vs. 50%, p < 0.05). In both groups, hBD-3 peptide was expressed not only in gingival keratinocytes, but also in Langerhans cells and Merkel cells. hBD-3 transcripts were detected in 90% of the samples and they were confined to the basal and/or suprabasal layers of gingival epithelia. Conclusions: This study shows that hBD-3 is frequently expressed in gingival epithelia. The appropriate expression of hBD-3 peptide may contribute to the maintenance of periodontal homeostasis, possibly through its antimicrobial effect and promotion of adaptive immune responses. © Blackwell Munksgaard 2005. | en_US |
dc.language | eng | en_US |
dc.publisher | Wiley-Blackwell Publishing, Inc.. The Journal's web site is located at http://www.wiley.com/bw/journal.asp?ref=0022-3484&site=1 | en_US |
dc.relation.ispartof | Journal of Periodontal Research | en_US |
dc.subject | Gingival epithelia | - |
dc.subject | Human β-defensin-3 | - |
dc.subject | Immunohistochemistry | - |
dc.subject | in situ hybridization | - |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Anti-Infective Agents - Analysis | en_US |
dc.subject.mesh | Antigens, Cd1 - Analysis | en_US |
dc.subject.mesh | Epithelium - Pathology | en_US |
dc.subject.mesh | Gingiva - Pathology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Intermediate Filament Proteins - Analysis | en_US |
dc.subject.mesh | Keratin-20 | en_US |
dc.subject.mesh | Keratinocytes - Pathology | en_US |
dc.subject.mesh | Langerhans Cells - Pathology | en_US |
dc.subject.mesh | Merkel Cells - Pathology | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Periodontal Pocket - Pathology | en_US |
dc.subject.mesh | Periodontitis - Pathology | en_US |
dc.subject.mesh | Beta-Defensins - Analysis | en_US |
dc.title | Expression of human β-defensin-3 in gingival epithelia | en_US |
dc.type | Article | en_US |
dc.identifier.email | Samaranayake, LP:lakshman@hku.hk | en_US |
dc.identifier.email | Jin, L:ljjin@hkucc.hku.hk | en_US |
dc.identifier.authority | Samaranayake, LP=rp00023 | en_US |
dc.identifier.authority | Jin, L=rp00028 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1111/j.1600-0765.2005.00827.x | en_US |
dc.identifier.pmid | 16302926 | - |
dc.identifier.scopus | eid_2-s2.0-27944437531 | en_US |
dc.identifier.hkuros | 112532 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-27944437531&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 40 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.spage | 474 | en_US |
dc.identifier.epage | 481 | en_US |
dc.identifier.isi | WOS:000232893600008 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Lu, Q=36128876000 | en_US |
dc.identifier.scopusauthorid | Samaranayake, LP=7102761002 | en_US |
dc.identifier.scopusauthorid | Darveau, RP=7006419856 | en_US |
dc.identifier.scopusauthorid | Jin, L=7403328850 | en_US |
dc.identifier.citeulike | 371826 | - |
dc.identifier.issnl | 0022-3484 | - |