Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1995-4-20
pubmed:abstractText
The ability of a range of skin commensal microorganisms to modulate interleukin-1 (IL-1) release by cultured human keratinocytes and peripheral blood mononuclear cells (PBMCs) was investigated by a combination of enzyme-linked immunosorbent assays and bioassays. Three fractions (formaldehyde-treated whole cells, culture supernatants, and cellular fractions) were prepared from Propionibacterium acnes, Propionibacterium granulosum, Staphylococcus epidermidis, Staphylococcus capitis, Staphylococcus hominis, and Malassezia furfur serovar B. The levels of immunochemical IL-1 alpha released by cultured keratinocytes during coincubations with these microbial fractions ranged from 0 to 136 pg/ml and were maximal after 72 h. No microbial fraction consistently upregulated immunochemical IL-1 alpha release by freshly isolated keratinocytes from two donors and a transformed cell line, all of which produced the cytokine constitutively to various extents. Bioassays revealed that most of the IL-1 released was biologically inactive. In contrast, whole cells of formaldehyde-treated P. granulosum and S. epidermidis significantly stimulated release of IL-1 beta by PBMCs from three donors compared with the negative control (culture medium). Release was maximal at 24 h. Coincubation with intact cells of the yeast M. furfur significantly decreased levels of IL-1 beta below the values for the negative control by PBMCs from all three donors. There was good correlation between bioassay data and immunoassay data for IL-1 beta, and the depressive effect of M. furfur cells on cytokine production by all three cultures of PBMCs was mirrored in the levels of bioactive cytokine. This reduction in IL-1 beta release by PBMCs by M. furfur may provide an explanation why dermatoses thought to be caused by this yeast are essentially noninflammatory or only mildly inflammatory.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-1534342, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-1535214, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-1554596, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-1576583, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-1670850, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-16788624, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-1720743, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-1890562, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-1999487, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2022885, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2090145, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2104245, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2254445, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2355179, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2431094, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2465548, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2529893, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-2969256, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3007615, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3022057, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3053905, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3106502, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3127333, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3161957, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3259579, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3261303, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3497177, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-3667925, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-5977762, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-6198387, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-6234376, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-6368372, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-6457823, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-6606682, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-6800841, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-6974195, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-6979588, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-7430000, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-8239612, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-8406805, http://linkedlifedata.com/resource/pubmed/commentcorrection/7890376-8423089
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0019-9567
pubmed:author
pubmed:issnType
Print
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1223-8
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1995
pubmed:articleTitle
In vitro modulation of keratinocyte-derived interleukin-1 alpha (IL-1 alpha) and peripheral blood mononuclear cell-derived IL-1 beta release in response to cutaneous commensal microorganisms.
pubmed:affiliation
Department of Microbiology, University of Leeds, United Kingdom.
pubmed:publicationType
Journal Article, In Vitro, Research Support, Non-U.S. Gov't