Immunohistochemical staining of skin-expressed proteins to identify exfoliated epidermal cells for forensic purposes.
Biomarkers
/ metabolism
Blood Chemical Analysis
Cervix Mucus
/ chemistry
DNA
/ analysis
Desmocollins
/ metabolism
Epidermal Cells
/ cytology
Filaggrin Proteins
Forensic Sciences
Humans
Immunohistochemistry
Intercellular Signaling Peptides and Proteins
/ metabolism
Intermediate Filament Proteins
/ metabolism
Kallikreins
/ metabolism
Keratin-10
/ metabolism
Real-Time Polymerase Chain Reaction
Saliva
/ chemistry
Semen
/ chemistry
Skin
/ metabolism
Staining and Labeling
Touch
Corneodesmosin
Desmocollin 1
Exfoliated epidermal cells
Immunohistochemistry
Touch DNA
Journal
Forensic science international
ISSN: 1872-6283
Titre abrégé: Forensic Sci Int
Pays: Ireland
ID NLM: 7902034
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
14
06
2019
revised:
05
08
2019
accepted:
22
08
2019
pubmed:
25
9
2019
medline:
20
12
2019
entrez:
25
9
2019
Statut:
ppublish
Résumé
The determination of cell type in biological casework samples would be helpful to identify the type of body fluids and interpret the DNA source in forensic laboratories. Exfoliated epidermal cells are considered to be a reasonable source of touch DNA; therefore, we developed and assessed an immunohistochemistry (IHC) procedure for identifying exfoliated epidermal cells as a screening test of touch DNA samples. Among five candidate protein markers investigated in this study, keratin 10 and kallikrein-related peptidase 5 were strongly expressed in the stratum corneum layer of the skin; however, their specificity was insufficient to identify epidermal cells. In contrast, IHC for corneodesmosin (CDSN), desmocollin 1 (DSC1), and filaggrin (FLG) was considered to be applicable because of their detectability and specificity on skin swab samples. Actually, CDSN and DSC1 could be good markers for exfoliated epidermal cells on touched contact traces that were contaminated with many unidentified impurities. Besides, positivity for FLG on mock casework samples appeared to be lower than for the other markers, which might be caused by its instability. Finally, the relationship between positivity for IHC and DNA yield was analyzed using skin swab samples. Although it was difficult to determine these correlations quantitatively because of the heterogeneous distribution of cells and the presence of cell-free DNA, the DNA-quantifiable samples analyzed in this study contained at least some of IHC-positive epidermal cells. In conclusion, IHC detection of skin-enriched proteins, especially CDSN and DSC1, could be useful for screening samples that have been handled or touched by someone before DNA analysis.
Identifiants
pubmed: 31550598
pii: S0379-0738(19)30352-4
doi: 10.1016/j.forsciint.2019.109940
pii:
doi:
Substances chimiques
Biomarkers
0
CDSN protein, human
0
DSC1 protein, human
0
Desmocollins
0
FLG protein, human
0
Filaggrin Proteins
0
Intercellular Signaling Peptides and Proteins
0
Intermediate Filament Proteins
0
KRT10 protein, human
0
Keratin-10
147785-83-9
DNA
9007-49-2
KLK5 protein, human
EC 3.4.21.-
Kallikreins
EC 3.4.21.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
109940Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.