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Conference Paper: Pseudomonas aeruginosa pyocyanin: discruption of ultrastructure of human respiratory mucosa in vitro
Title | Pseudomonas aeruginosa pyocyanin: discruption of ultrastructure of human respiratory mucosa in vitro |
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Authors | |
Issue Date | 2005 |
Publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/RES |
Citation | The 10th APSR Congress & the 1st Congress of the APSR/ACCP, Guangzhou, China, 11-14 November 2005. In Respirology, 2005, v. 10 n. S3, p. A126, abstract no. 170 How to Cite? |
Abstract | Purpose Previous studies showed that adenosine triphosphate (ATP) is
depleted from human respiratory epithelium in the presence of pyocyanin.
The latter was also associated with an increase in oxidative stress in
intracellular structures. It is postulated that mitochondrial ultrastructure would
be affected by pyocyanin.
Method The human respiratory mucosa was obtained without anaesthetic
from the inferior turbinate of 6 healthy subjects, and suspended in M199
which contained 0 and 20mg/mL of pyocyanin. After 4 hrs incubation, the
cells were fixed with 2.5% cacodylate-buffered glutaraldehyde and post-fixed
in 1% osmium tetroxide. This was followed by standard serial dehydration
through alcohols and embedding in araldite. An ultrathin section (70 to
90 nm) through the central portion of each specimen was examined with
TEM at a magnification of x3000, which is the lowest magnification for
mitochondria to be recognized. Ten digital images from each treatment were
captured for every subject. Total mitochondrial volume of each ultrathin
section was measured to be the area within the electronically traced area
using the Photopro plus programme.
Results Paired Sample t-test showed that there were significantly more swollen
mitochondria in TEM sections in the pyocyanin-treated epithelial cells
(p < 0.0001). Besides an increase in mitochondrial swelling, there was no
damage of cell junctions or loss of cilia and the orientation of cilia were
normal in the pyocyanin-treated epithelial cells.
Conclusion It is concluded that pyocyanin causes mitochondrial
ultrastructure damage. |
Persistent Identifier | http://hdl.handle.net/10722/95505 |
ISSN | 2023 Impact Factor: 6.6 2023 SCImago Journal Rankings: 1.559 |
DC Field | Value | Language |
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dc.contributor.author | Kwok, RP | en_HK |
dc.contributor.author | Sun, JZ | en_HK |
dc.contributor.author | Tipoe, GL | en_HK |
dc.contributor.author | Leung, YH | en_HK |
dc.contributor.author | Yan, CPK | en_HK |
dc.contributor.author | Ooi, CGC | en_HK |
dc.contributor.author | Ho, PL | en_HK |
dc.contributor.author | Mak, JCW | en_HK |
dc.contributor.author | Lam, WK | en_HK |
dc.contributor.author | Tsang, KWT | en_HK |
dc.date.accessioned | 2010-09-25T16:04:23Z | - |
dc.date.available | 2010-09-25T16:04:23Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | The 10th APSR Congress & the 1st Congress of the APSR/ACCP, Guangzhou, China, 11-14 November 2005. In Respirology, 2005, v. 10 n. S3, p. A126, abstract no. 170 | en_HK |
dc.identifier.issn | 1323-7799 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/95505 | - |
dc.description.abstract | Purpose Previous studies showed that adenosine triphosphate (ATP) is depleted from human respiratory epithelium in the presence of pyocyanin. The latter was also associated with an increase in oxidative stress in intracellular structures. It is postulated that mitochondrial ultrastructure would be affected by pyocyanin. Method The human respiratory mucosa was obtained without anaesthetic from the inferior turbinate of 6 healthy subjects, and suspended in M199 which contained 0 and 20mg/mL of pyocyanin. After 4 hrs incubation, the cells were fixed with 2.5% cacodylate-buffered glutaraldehyde and post-fixed in 1% osmium tetroxide. This was followed by standard serial dehydration through alcohols and embedding in araldite. An ultrathin section (70 to 90 nm) through the central portion of each specimen was examined with TEM at a magnification of x3000, which is the lowest magnification for mitochondria to be recognized. Ten digital images from each treatment were captured for every subject. Total mitochondrial volume of each ultrathin section was measured to be the area within the electronically traced area using the Photopro plus programme. Results Paired Sample t-test showed that there were significantly more swollen mitochondria in TEM sections in the pyocyanin-treated epithelial cells (p < 0.0001). Besides an increase in mitochondrial swelling, there was no damage of cell junctions or loss of cilia and the orientation of cilia were normal in the pyocyanin-treated epithelial cells. Conclusion It is concluded that pyocyanin causes mitochondrial ultrastructure damage. | - |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Asia. The Journal's web site is located at http://www.blackwellpublishing.com/journals/RES | en_HK |
dc.relation.ispartof | Respirology | en_HK |
dc.title | Pseudomonas aeruginosa pyocyanin: discruption of ultrastructure of human respiratory mucosa in vitro | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1323-7799&volume=10 &issue=Suppl&spage=A126 (#170)&epage=&date=2005&atitle=Pseudomonas+aeruginosa+pyocyanin+:+discruption+of+ultrastructure+of+human+respiratory+mucosa+in+vitro | en_HK |
dc.identifier.email | Sun, JZ: jzsun@HKUCC.hku.hk | en_HK |
dc.identifier.email | Tipoe, GL: tgeorge@hkucc.hku.hk | en_HK |
dc.identifier.email | Leung, YH: yhleung@HKUCC.hku.hk | en_HK |
dc.identifier.email | Yan, CPK: cpkyan@HKUSUA.hku.hk | en_HK |
dc.identifier.email | Ooi, CGC: cgcooi@hkucc.hku.hk | en_HK |
dc.identifier.email | Ho, PL: plho@hkucc.hku.hk | en_HK |
dc.identifier.email | Mak, JCW: judymak@HKUCC.hku.hk | en_HK |
dc.identifier.email | Lam, WK: lamwk@hku.hk | en_HK |
dc.identifier.email | Tsang, KWT: kwttsang@hku.hk | en_HK |
dc.identifier.authority | Tipoe, GL=rp00371 | en_HK |
dc.identifier.authority | Ho, PL=rp00406 | en_HK |
dc.identifier.authority | Mak, JCW=rp00352 | en_HK |
dc.identifier.hkuros | 122173 | en_HK |
dc.identifier.volume | 10 | en_HK |
dc.identifier.issue | suppl. 3 | en_HK |
dc.identifier.spage | A126, abstract no. 170 | en_HK |
dc.identifier.epage | A126, abstract no. 170 | - |
dc.identifier.issnl | 1323-7799 | - |