Cargando…
Nano‐Pulse Stimulation Induces Changes in the Intracellular Organelles in Rat Liver Tumors Treated In Situ
BACKGROUND AND OBJECTIVES: Nano‐pulse stimulation (NPS) therapy is the application of ultrafast pulses of high amplitude electrical energy to tissues to influence cell function. Unique characteristics of these pulses enable electric field penetration into the interior of cells and organelles to gene...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586959/ https://www.ncbi.nlm.nih.gov/pubmed/32220023 http://dx.doi.org/10.1002/lsm.23239 |
_version_ | 1783600093762420736 |
---|---|
author | Nuccitelli, Richard McDaniel, Amanda Connolly, Richard Zelickson, Brian Hartman, Holly |
author_facet | Nuccitelli, Richard McDaniel, Amanda Connolly, Richard Zelickson, Brian Hartman, Holly |
author_sort | Nuccitelli, Richard |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Nano‐pulse stimulation (NPS) therapy is the application of ultrafast pulses of high amplitude electrical energy to tissues to influence cell function. Unique characteristics of these pulses enable electric field penetration into the interior of cells and organelles to generate transient nanopores in both organelle and plasma membranes. The purpose of this study is to document the temporal and physical changes in intracellular organelles following NPS therapy using electron microscopy. STUDY DESIGN/MATERIALS AND METHODS: Liver tumors were induced in five buffalo rats by implanting syngeneic McA‐RH7777 hepatocellular carcinoma cells into the surgically exposed livers. Tumors were allowed to grow for 1 week and then the surgically exposed livers were treated in situ with NPS energy delivered at a sufficient level to trigger regulated cell death in the tumor. Samples of NPS‐treated and control tissue were removed and fixed for electron microscopy at 1 minute, 5 minutes, 30 minutes, 2 hours and 4 hours after exposure. RESULTS: Measurements of cellular organelles indicate strong swelling following NPS therapy exposure compared with untreated controls. The mean diameter of the mitochondria increased by 55% within 1 minute and then by 2.5‐fold by 2 hours post‐NPS therapy. The rough endoplasmic reticulum (RER) cisternae swelled immediately after NPS therapy with reduced swelling by 30 minutes and loss of structural integrity by 2 hours. The Golgi apparatus appears swollen in images collected 1 and 5 minutes after NPS therapy and was no longer detected at 30 minutes and 2 hours post‐NPS therapy. By 4 hours after NPS therapy, a nascent Golgi apparatus was detected in many of the images. The plasma membrane lost its well‐defined morphology and became less linear, exhibiting discontinuities as early as 1 minute post‐NPS energy exposure and the nuclear envelope became subjectively less distinct over time. CONCLUSIONS: NPS therapy at sufficient energy levels causes the rapid swelling of organelles, disintegration of the RER, breaks in the plasma membrane and blurs the borders of the nuclear envelope. These changes in the mitochondria and RER are indicative of a regulated cell death process. These immediate physical changes to vital cell organelles are likely to trigger subsequent regulated cell death mechanisms observed in other studies of NPS therapy. Lasers Surg. Med. © 2020 The Authors. Lasers in Surgery and Medicine published by Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-7586959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75869592020-10-30 Nano‐Pulse Stimulation Induces Changes in the Intracellular Organelles in Rat Liver Tumors Treated In Situ Nuccitelli, Richard McDaniel, Amanda Connolly, Richard Zelickson, Brian Hartman, Holly Lasers Surg Med Preclinical Reports BACKGROUND AND OBJECTIVES: Nano‐pulse stimulation (NPS) therapy is the application of ultrafast pulses of high amplitude electrical energy to tissues to influence cell function. Unique characteristics of these pulses enable electric field penetration into the interior of cells and organelles to generate transient nanopores in both organelle and plasma membranes. The purpose of this study is to document the temporal and physical changes in intracellular organelles following NPS therapy using electron microscopy. STUDY DESIGN/MATERIALS AND METHODS: Liver tumors were induced in five buffalo rats by implanting syngeneic McA‐RH7777 hepatocellular carcinoma cells into the surgically exposed livers. Tumors were allowed to grow for 1 week and then the surgically exposed livers were treated in situ with NPS energy delivered at a sufficient level to trigger regulated cell death in the tumor. Samples of NPS‐treated and control tissue were removed and fixed for electron microscopy at 1 minute, 5 minutes, 30 minutes, 2 hours and 4 hours after exposure. RESULTS: Measurements of cellular organelles indicate strong swelling following NPS therapy exposure compared with untreated controls. The mean diameter of the mitochondria increased by 55% within 1 minute and then by 2.5‐fold by 2 hours post‐NPS therapy. The rough endoplasmic reticulum (RER) cisternae swelled immediately after NPS therapy with reduced swelling by 30 minutes and loss of structural integrity by 2 hours. The Golgi apparatus appears swollen in images collected 1 and 5 minutes after NPS therapy and was no longer detected at 30 minutes and 2 hours post‐NPS therapy. By 4 hours after NPS therapy, a nascent Golgi apparatus was detected in many of the images. The plasma membrane lost its well‐defined morphology and became less linear, exhibiting discontinuities as early as 1 minute post‐NPS energy exposure and the nuclear envelope became subjectively less distinct over time. CONCLUSIONS: NPS therapy at sufficient energy levels causes the rapid swelling of organelles, disintegration of the RER, breaks in the plasma membrane and blurs the borders of the nuclear envelope. These changes in the mitochondria and RER are indicative of a regulated cell death process. These immediate physical changes to vital cell organelles are likely to trigger subsequent regulated cell death mechanisms observed in other studies of NPS therapy. Lasers Surg. Med. © 2020 The Authors. Lasers in Surgery and Medicine published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2020-03-27 2020-11 /pmc/articles/PMC7586959/ /pubmed/32220023 http://dx.doi.org/10.1002/lsm.23239 Text en © 2020 The Authors. Lasers in Surgery and Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Preclinical Reports Nuccitelli, Richard McDaniel, Amanda Connolly, Richard Zelickson, Brian Hartman, Holly Nano‐Pulse Stimulation Induces Changes in the Intracellular Organelles in Rat Liver Tumors Treated In Situ |
title | Nano‐Pulse Stimulation Induces Changes in the Intracellular Organelles in Rat Liver Tumors Treated In Situ |
title_full | Nano‐Pulse Stimulation Induces Changes in the Intracellular Organelles in Rat Liver Tumors Treated In Situ |
title_fullStr | Nano‐Pulse Stimulation Induces Changes in the Intracellular Organelles in Rat Liver Tumors Treated In Situ |
title_full_unstemmed | Nano‐Pulse Stimulation Induces Changes in the Intracellular Organelles in Rat Liver Tumors Treated In Situ |
title_short | Nano‐Pulse Stimulation Induces Changes in the Intracellular Organelles in Rat Liver Tumors Treated In Situ |
title_sort | nano‐pulse stimulation induces changes in the intracellular organelles in rat liver tumors treated in situ |
topic | Preclinical Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586959/ https://www.ncbi.nlm.nih.gov/pubmed/32220023 http://dx.doi.org/10.1002/lsm.23239 |
work_keys_str_mv | AT nuccitellirichard nanopulsestimulationinduceschangesintheintracellularorganellesinratlivertumorstreatedinsitu AT mcdanielamanda nanopulsestimulationinduceschangesintheintracellularorganellesinratlivertumorstreatedinsitu AT connollyrichard nanopulsestimulationinduceschangesintheintracellularorganellesinratlivertumorstreatedinsitu AT zelicksonbrian nanopulsestimulationinduceschangesintheintracellularorganellesinratlivertumorstreatedinsitu AT hartmanholly nanopulsestimulationinduceschangesintheintracellularorganellesinratlivertumorstreatedinsitu |