Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugs
The trypanosomatid cytoskeleton is responsible for the parasite's shape and it is modulated throughout the different stages of the parasite's life cycle. When parasites are exposed to media with reduced osmolarity, they initially swell, but subsequently undergo compensatory shrinking refer...
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Instituto Oswaldo Cruz, Ministério da Saúde
2013-02-01
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doaj-02583a592725438aa3088a7651a41b192020-11-24T23:14:15ZengInstituto Oswaldo Cruz, Ministério da SaúdeMemórias do Instituto Oswaldo Cruz.1678-80602013-02-011081849010.1590/S0074-02762013000100014S0074-02762013000100014Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugsFrancehuli Dagger0Elizabeth Valdivieso1Ana K Marcano2Carlos Ayesta3Universidad Central de VenezuelaUniversidad Central de VenezuelaUniversidad Central de VenezuelaUniversidad Central de VenezuelaThe trypanosomatid cytoskeleton is responsible for the parasite's shape and it is modulated throughout the different stages of the parasite's life cycle. When parasites are exposed to media with reduced osmolarity, they initially swell, but subsequently undergo compensatory shrinking referred to as regulatory volume decrease (RVD). We studied the effects of anti-microtubule (Mt) drugs on the proliferation of Leishmania mexicana promastigotes and their capacity to undergo RVD. All of the drugs tested exerted antiproliferative effects of varying magnitudes [ansamitocin P3 (AP3)> trifluoperazine > taxol > rhizoxin > chlorpromazine]. No direct relationship was found between antiproliferative drug treatment and RVD. Similarly, Mt stability was not affected by drug treatment. Ansamitocin P3, which is effective at nanomolar concentrations, blocked amastigote-promastigote differentiation and was the only drug that impeded RVD, as measured by light dispersion. AP3 induced 2 kinetoplasts (Kt) 1 nucleus cells that had numerous flagella-associated Kts throughout the cell. These results suggest that the dramatic morphological changes induced by AP3 alter the spatial organisation and directionality of the Mts that are necessary for the parasite's hypotonic stress-induced shape change, as well as its recovery.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762013000100014&lng=en&tlng=enmicrotubulesdrugsLeishmaniaregulatory volume decrease |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Francehuli Dagger Elizabeth Valdivieso Ana K Marcano Carlos Ayesta |
spellingShingle |
Francehuli Dagger Elizabeth Valdivieso Ana K Marcano Carlos Ayesta Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugs Memórias do Instituto Oswaldo Cruz. microtubules drugs Leishmania regulatory volume decrease |
author_facet |
Francehuli Dagger Elizabeth Valdivieso Ana K Marcano Carlos Ayesta |
author_sort |
Francehuli Dagger |
title |
Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugs |
title_short |
Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugs |
title_full |
Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugs |
title_fullStr |
Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugs |
title_full_unstemmed |
Regulatory volume decrease in Leishmania mexicana: effect of anti-microtubule drugs |
title_sort |
regulatory volume decrease in leishmania mexicana: effect of anti-microtubule drugs |
publisher |
Instituto Oswaldo Cruz, Ministério da Saúde |
series |
Memórias do Instituto Oswaldo Cruz. |
issn |
1678-8060 |
publishDate |
2013-02-01 |
description |
The trypanosomatid cytoskeleton is responsible for the parasite's shape and it is modulated throughout the different stages of the parasite's life cycle. When parasites are exposed to media with reduced osmolarity, they initially swell, but subsequently undergo compensatory shrinking referred to as regulatory volume decrease (RVD). We studied the effects of anti-microtubule (Mt) drugs on the proliferation of Leishmania mexicana promastigotes and their capacity to undergo RVD. All of the drugs tested exerted antiproliferative effects of varying magnitudes [ansamitocin P3 (AP3)> trifluoperazine > taxol > rhizoxin > chlorpromazine]. No direct relationship was found between antiproliferative drug treatment and RVD. Similarly, Mt stability was not affected by drug treatment. Ansamitocin P3, which is effective at nanomolar concentrations, blocked amastigote-promastigote differentiation and was the only drug that impeded RVD, as measured by light dispersion. AP3 induced 2 kinetoplasts (Kt) 1 nucleus cells that had numerous flagella-associated Kts throughout the cell. These results suggest that the dramatic morphological changes induced by AP3 alter the spatial organisation and directionality of the Mts that are necessary for the parasite's hypotonic stress-induced shape change, as well as its recovery. |
topic |
microtubules drugs Leishmania regulatory volume decrease |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762013000100014&lng=en&tlng=en |
work_keys_str_mv |
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