Biophysical analysis of astrocytes apoptosis triggered by larval E/S antigen from cerebral toxocarosis-causing pathogen Toxocara canis

Wesley W. Hsiao, Hsien Shun Liao, Hsing Hung Lin, Yueh Lun Lee, Chia Kwung Fan, Chien Wei Liao, Po Yen Lin, En Te Hwu, Chia Seng Chang

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Toxocarosis is a zoonosis caused by the transmission of the Toxocara canis (T. canis) larvae to humans. Its infectious third-stage larvae can invade the brains of paratenic hosts. The resultant brain damage can result in cerebral toxocarosis (CT). Astrocytes have important neurotrophic and neuroprotective functions in the brain. Substantial studies have shown that astrocyte apoptosis may contribute to the pathogenesis of many acute and chronic neurodegenerative disorders. We propose an alternation detection method, a combination of the astigmatic detection microscopy (ADM) and atomic force microscopy (AFM) techniques, to investigate the apoptosis of astrocytes triggered with T. canis larval excretory/secretory (Tc E/S) antigen. The variation in the pathology of a cell's morphological changes was investigated with ADM and AFM analyses and then confirmed by western blotting. The results showed that the round cells increased as the concentration of Tc E/S antigen and incubated time increased. In addition, the mean height of apoptotic cells was approximately twice that of untreated normal cells, which meant there was correlation between the Tc E/S antigen treatment and cell height. For each cleaved caspase-3 in the cells cocultured with Tc E/S antigen and incubated for 9 h, the corresponding intensities increased about 34-fold (34.4 ± 1.8) compared with those of the control cells. This method can provide researchers with a perspective for understanding the limited information on the mechanism of astroglial injury and death during a T. canis larval invasion in a brain infection.

Original languageEnglish
Pages (from-to)885-892
Number of pages8
JournalAnalytical Sciences
Volume29
Issue number9
DOIs
Publication statusPublished - 2013

Fingerprint

Pathogens
Brain
Apoptosis
Antigens
Atomic force microscopy
Microscopic examination
Pathology
Caspase 3
Cells
Astrocytes

Keywords

  • Apoptosis
  • Astigmatic detection microscopy (ADM)
  • Astrocytes
  • Atomic force microscopy (AFM)
  • T. canis larval excretory/secretory (Tc E/S) antigen
  • Toxocara canis (T. canis)
  • Toxocarosis

ASJC Scopus subject areas

  • Analytical Chemistry

Cite this

Biophysical analysis of astrocytes apoptosis triggered by larval E/S antigen from cerebral toxocarosis-causing pathogen Toxocara canis. / Hsiao, Wesley W.; Liao, Hsien Shun; Lin, Hsing Hung; Lee, Yueh Lun; Fan, Chia Kwung; Liao, Chien Wei; Lin, Po Yen; Hwu, En Te; Chang, Chia Seng.

In: Analytical Sciences, Vol. 29, No. 9, 2013, p. 885-892.

Research output: Contribution to journalArticle

Hsiao, Wesley W. ; Liao, Hsien Shun ; Lin, Hsing Hung ; Lee, Yueh Lun ; Fan, Chia Kwung ; Liao, Chien Wei ; Lin, Po Yen ; Hwu, En Te ; Chang, Chia Seng. / Biophysical analysis of astrocytes apoptosis triggered by larval E/S antigen from cerebral toxocarosis-causing pathogen Toxocara canis. In: Analytical Sciences. 2013 ; Vol. 29, No. 9. pp. 885-892.
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T1 - Biophysical analysis of astrocytes apoptosis triggered by larval E/S antigen from cerebral toxocarosis-causing pathogen Toxocara canis

AU - Hsiao, Wesley W.

AU - Liao, Hsien Shun

AU - Lin, Hsing Hung

AU - Lee, Yueh Lun

AU - Fan, Chia Kwung

AU - Liao, Chien Wei

AU - Lin, Po Yen

AU - Hwu, En Te

AU - Chang, Chia Seng

PY - 2013

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N2 - Toxocarosis is a zoonosis caused by the transmission of the Toxocara canis (T. canis) larvae to humans. Its infectious third-stage larvae can invade the brains of paratenic hosts. The resultant brain damage can result in cerebral toxocarosis (CT). Astrocytes have important neurotrophic and neuroprotective functions in the brain. Substantial studies have shown that astrocyte apoptosis may contribute to the pathogenesis of many acute and chronic neurodegenerative disorders. We propose an alternation detection method, a combination of the astigmatic detection microscopy (ADM) and atomic force microscopy (AFM) techniques, to investigate the apoptosis of astrocytes triggered with T. canis larval excretory/secretory (Tc E/S) antigen. The variation in the pathology of a cell's morphological changes was investigated with ADM and AFM analyses and then confirmed by western blotting. The results showed that the round cells increased as the concentration of Tc E/S antigen and incubated time increased. In addition, the mean height of apoptotic cells was approximately twice that of untreated normal cells, which meant there was correlation between the Tc E/S antigen treatment and cell height. For each cleaved caspase-3 in the cells cocultured with Tc E/S antigen and incubated for 9 h, the corresponding intensities increased about 34-fold (34.4 ± 1.8) compared with those of the control cells. This method can provide researchers with a perspective for understanding the limited information on the mechanism of astroglial injury and death during a T. canis larval invasion in a brain infection.

AB - Toxocarosis is a zoonosis caused by the transmission of the Toxocara canis (T. canis) larvae to humans. Its infectious third-stage larvae can invade the brains of paratenic hosts. The resultant brain damage can result in cerebral toxocarosis (CT). Astrocytes have important neurotrophic and neuroprotective functions in the brain. Substantial studies have shown that astrocyte apoptosis may contribute to the pathogenesis of many acute and chronic neurodegenerative disorders. We propose an alternation detection method, a combination of the astigmatic detection microscopy (ADM) and atomic force microscopy (AFM) techniques, to investigate the apoptosis of astrocytes triggered with T. canis larval excretory/secretory (Tc E/S) antigen. The variation in the pathology of a cell's morphological changes was investigated with ADM and AFM analyses and then confirmed by western blotting. The results showed that the round cells increased as the concentration of Tc E/S antigen and incubated time increased. In addition, the mean height of apoptotic cells was approximately twice that of untreated normal cells, which meant there was correlation between the Tc E/S antigen treatment and cell height. For each cleaved caspase-3 in the cells cocultured with Tc E/S antigen and incubated for 9 h, the corresponding intensities increased about 34-fold (34.4 ± 1.8) compared with those of the control cells. This method can provide researchers with a perspective for understanding the limited information on the mechanism of astroglial injury and death during a T. canis larval invasion in a brain infection.

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KW - Toxocara canis (T. canis)

KW - Toxocarosis

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