Literature DB >> 33664336

Machine learning-based classification of mitochondrial morphology in primary neurons and brain.

Garrett M Fogo1,2, Anthony R Anzell1,3,4, Kathleen J Maheras1, Sarita Raghunayakula1, Joseph M Wider1, Katlynn J Emaus1,2, Timothy D Bryson1,5, Melissa J Bukowski3, Robert W Neumar1, Karin Przyklenk3, Thomas H Sanderson6,7,8,9.   

Abstract

The mitochondrial network continually undergoes events of fission and fusion. Under physiologic conditions, the network is in equilibrium and is characterized by the presence of both elongated and punctate mitochondria. However, this balanced, homeostatic mitochondrial profile can change morphologic distribution in response to various stressors. Therefore, it is imperative to develop a method that robustly measures mitochondrial morphology with high accuracy. Here, we developed a semi-automated image analysis pipeline for the quantitation of mitochondrial morphology for both in vitro and in vivo applications. The image analysis pipeline was generated and validated utilizing images of primary cortical neurons from transgenic mice, allowing genetic ablation of key components of mitochondrial dynamics. This analysis pipeline was further extended to evaluate mitochondrial morphology in vivo through immunolabeling of brain sections as well as serial block-face scanning electron microscopy. These data demonstrate a highly specific and sensitive method that accurately classifies distinct physiological and pathological mitochondrial morphologies. Furthermore, this workflow employs the use of readily available, free open-source software designed for high throughput image processing, segmentation, and analysis that is customizable to various biological models.

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Year:  2021        PMID: 33664336      PMCID: PMC7933342          DOI: 10.1038/s41598-021-84528-8

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  58 in total

1.  Down-regulation of OPA1 alters mouse mitochondrial morphology, PTP function, and cardiac adaptation to pressure overload.

Authors:  Jerome Piquereau; Fanny Caffin; Marta Novotova; Alexandre Prola; Anne Garnier; Philippe Mateo; Dominique Fortin; Le Ha Huynh; Valérie Nicolas; Marcel V Alavi; Catherine Brenner; Renée Ventura-Clapier; Vladimir Veksler; Frédéric Joubert
Journal:  Cardiovasc Res       Date:  2012-03-08       Impact factor: 10.787

Review 2.  The interplay between mitochondrial dynamics and mitophagy.

Authors:  Gilad Twig; Orian S Shirihai
Journal:  Antioxid Redox Signal       Date:  2011-03-17       Impact factor: 8.401

3.  Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation.

Authors:  Angelika S Rambold; Brenda Kostelecky; Natalie Elia; Jennifer Lippincott-Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  2011-06-06       Impact factor: 11.205

Review 4.  Dynamin-related protein 1 and mitochondrial fragmentation in neurodegenerative diseases.

Authors:  P Hemachandra Reddy; Tejaswini P Reddy; Maria Manczak; Marcus J Calkins; Ulziibat Shirendeb; Peizhong Mao
Journal:  Brain Res Rev       Date:  2010-12-08

5.  The role of dynamin-related protein 1, a mediator of mitochondrial fission, in apoptosis.

Authors:  S Frank; B Gaume; E S Bergmann-Leitner; W W Leitner; E G Robert; F Catez; C L Smith; R J Youle
Journal:  Dev Cell       Date:  2001-10       Impact factor: 12.270

6.  Stimulation of glutamate receptors in cultured hippocampal neurons causes Ca2+-dependent mitochondrial contraction.

Authors:  Tatiana Brustovetsky; Viacheslav Li; Nickolay Brustovetsky
Journal:  Cell Calcium       Date:  2009-05-05       Impact factor: 6.817

7.  Calcium-induced mitochondrial swelling and cytochrome c release in the brain: its biochemical characteristics and implication in ischemic neuronal injury.

Authors:  Tohru Kobayashi; Satoshi Kuroda; Mitsuhiro Tada; Kiyohiro Houkin; Yoshinobu Iwasaki; Hiroshi Abe
Journal:  Brain Res       Date:  2003-01-17       Impact factor: 3.252

8.  Mitochondrial morphology regulates organellar Ca2+ uptake and changes cellular Ca2+ homeostasis.

Authors:  Alicia J Kowaltowski; Sergio L Menezes-Filho; Essam A Assali; Isabela G Gonçalves; João Victor Cabral-Costa; Phablo Abreu; Nathanael Miller; Patricia Nolasco; Francisco R M Laurindo; Alexandre Bruni-Cardoso; Orian S Shirihai
Journal:  FASEB J       Date:  2019-09-05       Impact factor: 5.834

9.  Dephosphorylation by calcineurin regulates translocation of Drp1 to mitochondria.

Authors:  G M Cereghetti; A Stangherlin; O Martins de Brito; C R Chang; C Blackstone; P Bernardi; L Scorrano
Journal:  Proc Natl Acad Sci U S A       Date:  2008-10-06       Impact factor: 11.205

10.  Early ERK1/2 activation promotes DRP1-dependent mitochondrial fission necessary for cell reprogramming.

Authors:  Javier Prieto; Marian León; Xavier Ponsoda; Ramón Sendra; Roque Bort; Raquel Ferrer-Lorente; Angel Raya; Carlos López-García; Josema Torres
Journal:  Nat Commun       Date:  2016-03-31       Impact factor: 14.919

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  3 in total

Review 1.  Revealing the Impact of Mitochondrial Fitness During Early Neural Development Using Human Brain Organoids.

Authors:  Alejandra I Romero-Morales; Vivian Gama
Journal:  Front Mol Neurosci       Date:  2022-04-29       Impact factor: 6.261

2.  Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons.

Authors:  Anthony R Anzell; Garrett M Fogo; Zoya Gurm; Sarita Raghunayakula; Joseph M Wider; Kathleen J Maheras; Katlynn J Emaus; Timothy D Bryson; Madison Wang; Robert W Neumar; Karin Przyklenk; Thomas H Sanderson
Journal:  Cell Death Dis       Date:  2021-05-12       Impact factor: 8.469

Review 3.  Assessing Drug-Induced Mitochondrial Toxicity in Cardiomyocytes: Implications for Preclinical Cardiac Safety Evaluation.

Authors:  Xiaoli Tang; Zengwu Wang; Shengshou Hu; Bingying Zhou
Journal:  Pharmaceutics       Date:  2022-06-21       Impact factor: 6.525

  3 in total

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