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Mefloquine causes selective mast cell apoptosis in cutaneous mastocytosis lesions by a secretory granule-mediated pathway

Lampinen, Maria (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Gastroenterologi/hepatologi,Klinisk kemi
Hagforsen, Eva (author)
Uppsala universitet,Dermatologi och venereologi
Weström, Simone (author)
Uppsala universitet,Dermatologi och venereologi,Institutionen för immunologi, genetik och patologi
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Bergström, Anna (author)
Uppsala universitet,Dermatologi och venereologi,Uppsala Univ Hosp, Dept Dermatol, Uppsala, Sweden.
Levedahl, Kerstin (author)
Uppsala universitet,Vårdvetenskap,Hematologi
Paivandy, Aida (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Lara-Valencia, Paola (author)
Uppsala universitet,Institutionen för immunologi, genetik och patologi
Pejler, Gunnar (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Rollman, Ola (author)
Uppsala universitet,Dermatologi och venereologi
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 (creator_code:org_t)
2022-08-04
2022
English.
In: Experimental dermatology. - : John Wiley & Sons. - 0906-6705 .- 1600-0625. ; 31:11, s. 1729-1740
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Mastocytosis is a KIT-related myeloproliferative disease characterised by abnormal expansion of neoplastic mast cells (MC) in the skin or virtually any other organ system. The cutaneous form of adult-onset mastocytosis is almost invariably combined with indolent systemic involvement for which curative therapy is yet not available. Here we evaluated a concept of depleting cutaneous MCs in mastocytosis lesions ex vivo by targeting their secretory granules. Skin biopsies from mastocytosis patients were incubated with or without mefloquine, an antimalarial drug known to penetrate into acidic organelles such as MC secretory granules. Mefloquine reduced the number of dermal MCs without affecting keratinocyte proliferation or epidermal gross morphology at drug concentrations up to 40 mu M. Flow cytometric analysis of purified dermal MCs showed that mefloquine-induced cell death was mainly due to apoptosis and accompanied by caspase-3 activation. However, caspase inhibition provided only partial protection against mefloquine-induced cell death, indicating predominantly caspase-independent apoptosis. Further assessments revealed that mefloquine caused an elevation of granule pH and a corresponding decrease in cytosolic pH, suggesting drug-induced granule permeabilisation. Extensive damage to the MC secretory granules was confirmed by transmission electron microscopy analysis. Further, blockade of granule acidification or serine protease activity prior to mefloquine treatment protected MCs from apoptosis, indicating that granule acidity and granule-localised serine proteases play major roles in the execution of mefloquine-induced cell death. Altogether, these findings reveal that mefloquine induces selective apoptosis of MCs by targeting their secretory granules and suggest that the drug may potentially extend its range of medical applications.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

apoptosis
mast cells
mastocytosis
mefloquine
secretory granules

Publication and Content Type

ref (subject category)
art (subject category)

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