The Fate of a Hapten - From the Skin to Modification of Macrophage Migration Inhibitory Factor (MIF) in Lymph Nodes.
Isabella KarlssonKristin SamuelssonCarl SimonssonAnna-Lena StenfeldtUlrika NilssonLeopold L IlagCharlotte JonssonAnn-Therese KarlbergPublished in: Scientific reports (2018)
Skin (contact) allergy, the most prevalent form of immunotoxicity in humans, is caused by low molecular weight chemicals (haptens) that penetrate stratum corneum and modify endogenous proteins. The fate of haptens after cutaneous absorption, especially what protein(s) they react with, is largely unknown. In this study the fluorescent hapten tetramethylrhodamine isothiocyanate (TRITC) was used to identify hapten-protein conjugates in the local lymph nodes after topical application, as they play a key role in activation of the adaptive immune system. TRITC interacted with dendritic cells but also with T and B cells in the lymph nodes as shown by flow cytometry. Identification of the most abundant TRITC-modified protein in lymph nodes by tandem mass spectrometry revealed TRITC-modification of the N-terminal proline of macrophage migration inhibitory factor (MIF) - an evolutionary well-conserved protein involved in cell-mediated immunity and inflammation. This is the first time a hapten-modified protein has been identified in lymph nodes after topical administration of the hapten. Most haptens are electrophiles and can therefore modify the N-terminal proline of MIF, which has an unusually reactive amino group under physiological conditions; thus, modification of MIF by haptens may have an immunomodulating role in contact allergy as well as in other immunotoxicity reactions.
Keyphrases
- lymph node
- dendritic cells
- protein protein
- flow cytometry
- neoadjuvant chemotherapy
- sentinel lymph node
- amino acid
- adipose tissue
- oxidative stress
- binding protein
- wound healing
- stem cells
- gene expression
- radiation therapy
- liquid chromatography
- dna methylation
- bone marrow
- high resolution
- soft tissue
- simultaneous determination
- mass spectrometry
- cell therapy
- quantum dots
- ms ms
- gas chromatography