Literature DB >> 26240532

In Vivo Time-Lapse Imaging in the Zebrafish Lateral Line: A Flexible, Open-Ended Research Project for an Undergraduate Neurobiology Laboratory Course.

Molly H Marra1, Zachary J C Tobias2, Hannah R Cohen2, Greta Glover3, Tamily A Weissman2.   

Abstract

The lateral line sensory system in fish detects movements in the water and allows fish to respond to predators, prey, and other stimuli. As the lateral line forms in the first two days of zebrafish development, axons extend caudally along the lateral surface of the fish, eventually forming synapses with hair cells of neuromasts. Growing lateral line axons are located superficially under the skin and can be labeled in living zebrafish using fluorescent protein expression. This system provides a relatively straightforward approach for in vivo time-lapse imaging of neuronal development in an undergraduate setting. Here we describe an upper-level neurobiology laboratory module in which students investigate aspects of axonal development in the zebrafish lateral line system. Students learn to handle and image living fish, collect time-lapse videos of moving mitochondria, and quantitatively measure mitochondrial dynamics by generating and analyzing kymographs of their movements. Energy demands may differ between axons with extending growth cones versus axons that have already reached their targets and are forming synapses. Since relatively little is known about this process in developing lateral line axons, students generate and test their own hypotheses regarding how mitochondrial dynamics may differ at two different time points in axonal development. Students also learn to incorporate into their analysis a powerful yet accessible quantitative tool, the kymograph, which is used to graph movement over time. After students measure and quantify dynamics in living fish at 1 and 2 days post fertilization, this module extends into independent projects, in which students can expand their studies in a number of different, inquiry-driven directions. The project can also be pared down for courses that wish to focus solely on the quantitative analysis (without fish handling), or vice versa. This research module provides a useful approach for the design of open-ended laboratory research projects that integrate the scientific process into undergraduate Biology courses, as encouraged by the AAAS and NSF Vision and Change Initiative.

Entities:  

Keywords:  axon development; fluorescence; growth cone; in vivo; lateral line; mitochondria; time-lapse imaging; zebrafish

Year:  2015        PMID: 26240532      PMCID: PMC4521740     

Source DB:  PubMed          Journal:  J Undergrad Neurosci Educ        ISSN: 1544-2896


  17 in total

1.  Towing of sensory axons by their migrating target cells in vivo.

Authors:  Darren Gilmour; Holger Knaut; Hans-Martin Maischein; Christiane Nüsslein-Volhard
Journal:  Nat Neurosci       Date:  2004-04-18       Impact factor: 24.884

Review 2.  Building the posterior lateral line system in zebrafish.

Authors:  Ajay B Chitnis; Damian Dalle Nogare; Miho Matsuda
Journal:  Dev Neurobiol       Date:  2012-03       Impact factor: 3.964

Review 3.  Axon and dendritic trafficking.

Authors:  Celine I Maeder; Kang Shen; Casper C Hoogenraad
Journal:  Curr Opin Neurobiol       Date:  2014-04-22       Impact factor: 6.627

4.  Stages of embryonic development of the zebrafish.

Authors:  C B Kimmel; W W Ballard; S R Kimmel; B Ullmann; T F Schilling
Journal:  Dev Dyn       Date:  1995-07       Impact factor: 3.780

Review 5.  Regulation of mitochondrial transport in neurons.

Authors:  Mei-Yao Lin; Zu-Hang Sheng
Journal:  Exp Cell Res       Date:  2015-01-19       Impact factor: 3.905

Review 6.  Anesthesia and euthanasia in zebrafish.

Authors:  Monte Matthews; Zoltán M Varga
Journal:  ILAR J       Date:  2012

7.  Sensory neuron growth cones comigrate with posterior lateral line primordial cells in zebrafish.

Authors:  W K Metcalfe
Journal:  J Comp Neurol       Date:  1985-08-08       Impact factor: 3.215

8.  Both pre- and postsynaptic activity of Nsf prevents degeneration of hair-cell synapses.

Authors:  Weike Mo; Teresa Nicolson
Journal:  PLoS One       Date:  2011-11-03       Impact factor: 3.240

9.  Using the Tg(nrd:egfp)/albino zebrafish line to characterize in vivo expression of neurod.

Authors:  Jennifer L Thomas; Margaret J Ochocinska; Peter F Hitchcock; Ryan Thummel
Journal:  PLoS One       Date:  2012-01-03       Impact factor: 3.240

10.  Axonal transport of mitochondria along microtubules and F-actin in living vertebrate neurons.

Authors:  R L Morris; P J Hollenbeck
Journal:  J Cell Biol       Date:  1995-12       Impact factor: 10.539

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  5 in total

1.  Open-Ended Inquiry into Zebrafish Nerve Development Using Image Analysis.

Authors:  Sarah C Petersen
Journal:  J Undergrad Neurosci Educ       Date:  2021-12-24

2.  Analyzing Mitochondrial Transport and Morphology in Human Induced Pluripotent Stem Cell-Derived Neurons in Hereditary Spastic Paraplegia.

Authors:  Yongchao Mou; Sukhada Mukte; Eric Chai; Joshua Dein; Xue-Jun Li
Journal:  J Vis Exp       Date:  2020-02-09       Impact factor: 1.355

3.  Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia.

Authors:  Yongchao Mou; Yi Dong; Zhenyu Chen; Kyle R Denton; Michael O Duff; Craig Blackstone; Su-Chun Zhang; Xue-Jun Li
Journal:  Acta Neuropathol Commun       Date:  2020-12-07       Impact factor: 7.801

4.  Mitochondrial and Neuronal Dysfunctions in L1 Mutant Mice.

Authors:  Ludovica Congiu; Viviana Granato; Gabriele Loers; Ralf Kleene; Melitta Schachner
Journal:  Int J Mol Sci       Date:  2022-04-14       Impact factor: 6.208

5.  First Year Course-Based Undergraduate Research Experience (CURE) Using the CRISPR/Cas9 Genome Engineering Technology in Zebrafish.

Authors:  Jay M Bhatt; Anil Kumar Challa
Journal:  J Microbiol Biol Educ       Date:  2017-01-29
  5 in total

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