Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis Infection

Infection with the roundworm Angiostrongylus cantonensis is the main cause of eosinophilic meningitis worldwide. The underlying molecular basis of the various pathological outcomes in permissive and non-permissive hosts infected with A. cantonensis remains poorly defined. In the present study, the h...

Full description

Bibliographic Details
Main Authors: Hongli Zhou, Zhe Chen, Yanin Limpanont, Yue Hu, Yubin Ma, Ping Huang, Paron Dekumyoy, Minyu Zhou, Yixin Cheng, Zhiyue Lv
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-01-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2019.03126/full
_version_ 1819262799109423104
author Hongli Zhou
Hongli Zhou
Hongli Zhou
Zhe Chen
Zhe Chen
Zhe Chen
Yanin Limpanont
Yue Hu
Yue Hu
Yue Hu
Yubin Ma
Yubin Ma
Yubin Ma
Ping Huang
Ping Huang
Ping Huang
Paron Dekumyoy
Minyu Zhou
Minyu Zhou
Minyu Zhou
Yixin Cheng
Yixin Cheng
Yixin Cheng
Zhiyue Lv
Zhiyue Lv
Zhiyue Lv
Zhiyue Lv
author_facet Hongli Zhou
Hongli Zhou
Hongli Zhou
Zhe Chen
Zhe Chen
Zhe Chen
Yanin Limpanont
Yue Hu
Yue Hu
Yue Hu
Yubin Ma
Yubin Ma
Yubin Ma
Ping Huang
Ping Huang
Ping Huang
Paron Dekumyoy
Minyu Zhou
Minyu Zhou
Minyu Zhou
Yixin Cheng
Yixin Cheng
Yixin Cheng
Zhiyue Lv
Zhiyue Lv
Zhiyue Lv
Zhiyue Lv
author_sort Hongli Zhou
collection DOAJ
description Infection with the roundworm Angiostrongylus cantonensis is the main cause of eosinophilic meningitis worldwide. The underlying molecular basis of the various pathological outcomes in permissive and non-permissive hosts infected with A. cantonensis remains poorly defined. In the present study, the histology of neurological disorders in the central nervous system (CNS) of infected rats was assessed by using hematoxylin and eosin staining. Quantitative reverse transcription polymerase chain reaction (RT-qPCR), western blot and immunofluorescence (IF) were used in evolutions of the transcription and translation levels of the apoptosis-, necroptosis-, autophagy-, and pyroptosis-related genes. The distribution of apoptotic and necroptotic cells in the rat hippocampus and parenchyma was further detected using flow cytometry, and the features of the ultrastructure of the cells were examined by transmission electron microscopy (TEM). The inflammatory response upon CNS infection with A. cantonensis evolved, as characterized by the accumulation of a small number of inflammatory cells under the thickened meninges, which peaked at 21 days post-infection (dpi) and returned to normal by 35 dpi. The transcription levels and translation of caspase-2, caspase-8, RIP1 and RIP3 increased significantly at 21 and 28 dpi but decreased sharply at 35 dpi compared to those in the normal control group. However, the changes in the expression of caspase-1, caspase-3, caspase-11, Beclin-1 and LC3B were not obvious, suggesting that apoptosis and necroptosis but not autophagy or pyroptosis occurred in the brains of infected animals at 21 and 28 dpi. The results of RT-qPCR, western blot analysis, IF, flow cytometry and TEM further illustrated that necroptosis and caspase-2-mediated apoptosis occurred in astrocytes and neurons but not in microglia in the parenchyma and hippocampus of infected animals. This study provides the first evidence that neuronal and astrocytic necroptosis and caspase-2-mediated apoptosis are induced by A. cantonensis infection in the parenchymal and hippocampal regions of rats at 21 and 28 dpi but these processes are negligible at 35 dpi. These findings enhance our understanding of the pathogenesis of A. cantonensis infection and provide new insights into therapeutic approaches targeting the occurrence of cell death in astrocytes and neurons in infected patients.
first_indexed 2024-12-23T20:03:26Z
format Article
id doaj.art-afa7af82307c43259a339ce23e33e385
institution Directory Open Access Journal
issn 1664-302X
language English
last_indexed 2024-12-23T20:03:26Z
publishDate 2020-01-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Microbiology
spelling doaj.art-afa7af82307c43259a339ce23e33e3852022-12-21T17:33:00ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2020-01-011010.3389/fmicb.2019.03126502946Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis InfectionHongli Zhou0Hongli Zhou1Hongli Zhou2Zhe Chen3Zhe Chen4Zhe Chen5Yanin Limpanont6Yue Hu7Yue Hu8Yue Hu9Yubin Ma10Yubin Ma11Yubin Ma12Ping Huang13Ping Huang14Ping Huang15Paron Dekumyoy16Minyu Zhou17Minyu Zhou18Minyu Zhou19Yixin Cheng20Yixin Cheng21Yixin Cheng22Zhiyue Lv23Zhiyue Lv24Zhiyue Lv25Zhiyue Lv26Joint Program of Pathobiology, The Fifth Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, ChinaKey Laboratory of Tropical Disease Control, Sun Yat-sen University, Ministry of Education, Guangzhou, ChinaKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, ChinaJoint Program of Pathobiology, The Fifth Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, ChinaKey Laboratory of Tropical Disease Control, Sun Yat-sen University, Ministry of Education, Guangzhou, ChinaKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, ChinaFaculty of Tropical Medicine, Mahidol University, Bangkok, ThailandJoint Program of Pathobiology, The Fifth Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, ChinaKey Laboratory of Tropical Disease Control, Sun Yat-sen University, Ministry of Education, Guangzhou, ChinaKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, ChinaJoint Program of Pathobiology, The Fifth Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, ChinaKey Laboratory of Tropical Disease Control, Sun Yat-sen University, Ministry of Education, Guangzhou, ChinaKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, ChinaJoint Program of Pathobiology, The Fifth Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, ChinaKey Laboratory of Tropical Disease Control, Sun Yat-sen University, Ministry of Education, Guangzhou, ChinaKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, ChinaFaculty of Tropical Medicine, Mahidol University, Bangkok, ThailandJoint Program of Pathobiology, The Fifth Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, ChinaKey Laboratory of Tropical Disease Control, Sun Yat-sen University, Ministry of Education, Guangzhou, ChinaKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, ChinaJoint Program of Pathobiology, The Fifth Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, ChinaKey Laboratory of Tropical Disease Control, Sun Yat-sen University, Ministry of Education, Guangzhou, ChinaKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, ChinaJoint Program of Pathobiology, The Fifth Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, ChinaKey Laboratory of Tropical Disease Control, Sun Yat-sen University, Ministry of Education, Guangzhou, ChinaKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Medical University, Haikou, ChinaGuangdong Provincial Key Laboratory of Biomedical Imaging, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, ChinaInfection with the roundworm Angiostrongylus cantonensis is the main cause of eosinophilic meningitis worldwide. The underlying molecular basis of the various pathological outcomes in permissive and non-permissive hosts infected with A. cantonensis remains poorly defined. In the present study, the histology of neurological disorders in the central nervous system (CNS) of infected rats was assessed by using hematoxylin and eosin staining. Quantitative reverse transcription polymerase chain reaction (RT-qPCR), western blot and immunofluorescence (IF) were used in evolutions of the transcription and translation levels of the apoptosis-, necroptosis-, autophagy-, and pyroptosis-related genes. The distribution of apoptotic and necroptotic cells in the rat hippocampus and parenchyma was further detected using flow cytometry, and the features of the ultrastructure of the cells were examined by transmission electron microscopy (TEM). The inflammatory response upon CNS infection with A. cantonensis evolved, as characterized by the accumulation of a small number of inflammatory cells under the thickened meninges, which peaked at 21 days post-infection (dpi) and returned to normal by 35 dpi. The transcription levels and translation of caspase-2, caspase-8, RIP1 and RIP3 increased significantly at 21 and 28 dpi but decreased sharply at 35 dpi compared to those in the normal control group. However, the changes in the expression of caspase-1, caspase-3, caspase-11, Beclin-1 and LC3B were not obvious, suggesting that apoptosis and necroptosis but not autophagy or pyroptosis occurred in the brains of infected animals at 21 and 28 dpi. The results of RT-qPCR, western blot analysis, IF, flow cytometry and TEM further illustrated that necroptosis and caspase-2-mediated apoptosis occurred in astrocytes and neurons but not in microglia in the parenchyma and hippocampus of infected animals. This study provides the first evidence that neuronal and astrocytic necroptosis and caspase-2-mediated apoptosis are induced by A. cantonensis infection in the parenchymal and hippocampal regions of rats at 21 and 28 dpi but these processes are negligible at 35 dpi. These findings enhance our understanding of the pathogenesis of A. cantonensis infection and provide new insights into therapeutic approaches targeting the occurrence of cell death in astrocytes and neurons in infected patients.https://www.frontiersin.org/article/10.3389/fmicb.2019.03126/fullAngiostrongylus cantonensisratapoptosisnecroptosiscaspase-2
spellingShingle Hongli Zhou
Hongli Zhou
Hongli Zhou
Zhe Chen
Zhe Chen
Zhe Chen
Yanin Limpanont
Yue Hu
Yue Hu
Yue Hu
Yubin Ma
Yubin Ma
Yubin Ma
Ping Huang
Ping Huang
Ping Huang
Paron Dekumyoy
Minyu Zhou
Minyu Zhou
Minyu Zhou
Yixin Cheng
Yixin Cheng
Yixin Cheng
Zhiyue Lv
Zhiyue Lv
Zhiyue Lv
Zhiyue Lv
Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis Infection
Frontiers in Microbiology
Angiostrongylus cantonensis
rat
apoptosis
necroptosis
caspase-2
title Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis Infection
title_full Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis Infection
title_fullStr Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis Infection
title_full_unstemmed Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis Infection
title_short Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis Infection
title_sort necroptosis and caspase 2 mediated apoptosis of astrocytes and neurons but not microglia of rat hippocampus and parenchyma caused by angiostrongylus cantonensis infection
topic Angiostrongylus cantonensis
rat
apoptosis
necroptosis
caspase-2
url https://www.frontiersin.org/article/10.3389/fmicb.2019.03126/full
work_keys_str_mv AT honglizhou necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT honglizhou necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT honglizhou necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT zhechen necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT zhechen necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT zhechen necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yaninlimpanont necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yuehu necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yuehu necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yuehu necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yubinma necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yubinma necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yubinma necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT pinghuang necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT pinghuang necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT pinghuang necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT parondekumyoy necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT minyuzhou necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT minyuzhou necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT minyuzhou necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yixincheng necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yixincheng necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT yixincheng necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT zhiyuelv necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT zhiyuelv necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT zhiyuelv necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection
AT zhiyuelv necroptosisandcaspase2mediatedapoptosisofastrocytesandneuronsbutnotmicrogliaofrathippocampusandparenchymacausedbyangiostrongyluscantonensisinfection