Interaction of Mycobacterium leprae with the HaCaT human keratinocyte cell line: new frontiers in the cellular immunology of leprosy. Issue 7 (4th May 2015)
- Record Type:
- Journal Article
- Title:
- Interaction of Mycobacterium leprae with the HaCaT human keratinocyte cell line: new frontiers in the cellular immunology of leprosy. Issue 7 (4th May 2015)
- Main Title:
- Interaction of Mycobacterium leprae with the HaCaT human keratinocyte cell line: new frontiers in the cellular immunology of leprosy
- Authors:
- Lyrio, Eloah C.D.
Campos‐Souza, Ivy C.
Corrêa, Luiz C.D.
Lechuga, Guilherme C.
Verícimo, Maurício
Castro, Helena C.
Bourguignon, Saulo C.
Côrte‐Real, Suzana
Ratcliffe, Norman
Declercq, Wim
Santos, Dilvani O. - Abstract:
- <abstract abstract-type="main" id="exd12714-abs-0001"> <title>Abstract</title> <p>Leprosy is a chronic granulomatous disease caused by <italic>Mycobacterium leprae</italic> affecting the skin and peripheral nerves. Despite <italic>M. leprae</italic> invasion of the skin and keratinocytes importance in innate immunity, the interaction of these cells <italic>in vitro</italic> during <italic>M. leprae</italic> infection is poorly understood. Conventional and fluorescence optical microscopy, transmission electronic microscopy, flow cytometry and ELISA were used to study the <italic>in vitro</italic> interaction of <italic>M. leprae</italic> with the HaCaT human keratinocyte cell line. Keratinocytes uptake of <italic>M. leprae</italic> is described, and modulation of the surface expression of CD80 and CD209, cathelicidin expression and TNF‐<italic>α</italic> and IL‐1<italic>β</italic> production of human keratinocytes are compared with dendritic cells and macrophages during <italic>M. leprae</italic> interaction. This study demonstrated that <italic>M. leprae</italic> interaction with human keratinocytes enhanced expression of cathelicidin and greatly increased TNF‐<italic>α</italic> production. The highest spontaneous expression of cathelicidin was by dendritic cells which are less susceptible to <italic>M. leprae</italic> infection. In contrast, keratinocytes displayed low spontaneous cathelicidin expression and were more susceptible to <italic>M. leprae</italic> infection than<abstract abstract-type="main" id="exd12714-abs-0001"> <title>Abstract</title> <p>Leprosy is a chronic granulomatous disease caused by <italic>Mycobacterium leprae</italic> affecting the skin and peripheral nerves. Despite <italic>M. leprae</italic> invasion of the skin and keratinocytes importance in innate immunity, the interaction of these cells <italic>in vitro</italic> during <italic>M. leprae</italic> infection is poorly understood. Conventional and fluorescence optical microscopy, transmission electronic microscopy, flow cytometry and ELISA were used to study the <italic>in vitro</italic> interaction of <italic>M. leprae</italic> with the HaCaT human keratinocyte cell line. Keratinocytes uptake of <italic>M. leprae</italic> is described, and modulation of the surface expression of CD80 and CD209, cathelicidin expression and TNF‐<italic>α</italic> and IL‐1<italic>β</italic> production of human keratinocytes are compared with dendritic cells and macrophages during <italic>M. leprae</italic> interaction. This study demonstrated that <italic>M. leprae</italic> interaction with human keratinocytes enhanced expression of cathelicidin and greatly increased TNF‐<italic>α</italic> production. The highest spontaneous expression of cathelicidin was by dendritic cells which are less susceptible to <italic>M. leprae</italic> infection. In contrast, keratinocytes displayed low spontaneous cathelicidin expression and were more susceptible to <italic>M. leprae</italic> infection than dendritic cells. The results show, for the first time, an active role for keratinocytes during infection by irradiated whole cells of <italic>M. leprae</italic> and the effect of vitamin D on this process. They also suggest that therapies which target cathelicidin modulation may provide novel approaches for treatment of leprosy.</p> </abstract> … (more)
- Is Part Of:
- Experimental dermatology. Volume 24:Issue 7(2015:Jul.)
- Journal:
- Experimental dermatology
- Issue:
- Volume 24:Issue 7(2015:Jul.)
- Issue Display:
- Volume 24, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 24
- Issue:
- 7
- Issue Sort Value:
- 2015-0024-0007-0000
- Page Start:
- 536
- Page End:
- 542
- Publication Date:
- 2015-05-04
- Subjects:
- Dermatology -- Periodicals
616.5 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=0906-6705&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-0625 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/exd.12714 ↗
- Languages:
- English
- ISSNs:
- 0906-6705
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3839.070000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3782.xml