microPublication

Get Your Data Out, Be Cited

  • About
    • Editorial Policies
      • Editorial Staff
      • Editorial Board
      • Criteria For Publication
      • Publishing Information
      • Data Sharing Policy
    • For Authors
      • Preparation And Submission Of A Manuscript
      • Peer Review Process
      • Following Acceptance
      • Appeals
    • For Reviewers
    • Why micropublish?
  • Submit a microPublication
  • Journals
    • microPublication Biology
      • Editorial Board
  • microPublications
    • Biology
      • Species
        • Arabidopsis
        • C. elegans
        • D. discoideum
        • Drosophila
        • Human
        • Mouse
        • S. cerevisiae
        • S. pombe
        • Xenopus
        • Zebrafish
      • Categories
        • Phenotype Data
        • Methods
        • Expression Data
        • Genotype Data
        • Integrations
        • Genetic Screens
        • Models of Human Disease
        • Software
        • Interaction data
        • Database Updates
        • Electrophysiology Data
        • Phylogenetic Data
        • Science and Society
        • Biochemistry
  • Contact
  • More
    • Archives
    • FAQs
    • Newsletter
microPublication / Biology / The bodies of dpy-10(e128) are...
The bodies of dpy-10(e128) are twice as stiff as wild type
Sylvia Fechner1, Frédéric Loizeau2, Adam L. Nekimken1,2, Beth L. Pruitt2,3 and Miriam B. Goodman1
1Molecular and Cellular Physiology, Stanford School of Medicine, Stanford
2Departments of Bioengineering and Mechanical Engineering, Stanford
3Departments of Mechanical Engineering and Biomolecular Science and Engineering, University of California, Santa Barbara
Correspondence to: Sylvia Fechner (sfechner@stanford.edu)
Panel A shows the force and indentation produced in response to a mechanical load applied by pushing a glass bead mounted on a self-sensing cantilever into the worm’s body. Panel B shows a set of 45 force and indentation pulses to determine the overall relationship between force and indentation for a dpy-10 (gray) and a wild-type (N2, black) L4 or young adult hermaphrodite. The force-indentation plots were fitted with a line where the slope is taken as a measure of body stiffness. Panels C-E show the measurements derived from more than 20 animals and the red bar indicates mean ± standard deviation.

Description

DPY-10 is a collagen protein in the nematode’s cuticle. Mutations in the dpy-10 gene induce various morphological changes that lead to animals with a dumpy (Dpy) or roller (Rol) phenotype (Levy, Yang & Kramer, 1993). Here, we asked how such mutations affect body stiffness by comparing force-indentation curves in dpy-10(e128) and wild type worms. On average, dpy-10(e128) worms have a steeper force-indentation relationship, leading to a higher body stiffness (Fig 1C). Average stiffness values were 2.5 ± 0.9 N/m, SD, (n = 24) for dpy-10(e128) and 0.9 ± 0.3 N/m, SD, (n = 25) for wild type (N2) hermaphrodites. Qualitatively, we observed that some of the dpy-10(e128) worms had a disrupted cuticle and their bodies spontaneously eviscerated after being immobilized to an agarose pad. Finally, we confirm the finding that dpy-10(e128) worms are shorter (Fig 1D) and fatter (Fig 1E) than wild type worms with an average body length of 712 ± 68 µm (SD, n = 24) compared to wild type N2 worms 900 ± 68 µm (SD, n = 25) and an average body width at the pharynx of 42 ± 5.6 µm (SD, n = 24) compared to wild type N2 worms 36 ± 4 µm (SD, n = 25) (Levy, Yang & Kramer, 1993). Figure 1F shows body shape and size of the two genotypes (drawn to scale).

From these results, we conclude that the bodies of dpy-10(e128) are twice as stiff as wild type: to reach the same indentation, a much higher force was necessary to be applied to dpy-10(e128) than to wild type worms (Fig 1A). Prior measurements of body stiffness with the same method revealed that dpy-5(e61) worms are softer than wild type worms (Park et al. 2007). Thus, body shape does not predict body stiffness. Why is one Dpy animal softer than wild-type and another one stiffer? We propose that dpy-10 is stiffer than wild type because it has an increased internal glycerol concentration and increased pressure, that is absent from dpy-5(e61) (Wheeler and Thomas 2006).

Methods

Request a detailed protocol

Preparation of worms: Age-synchronized C. elegans nematodes were grown on standard OP50 growth plates at 20–23 °C. Late L4 or young adult hermaphrodites were immobilized on 8% agarose pads using WormGlu (GluStitch). During the experiments the worms were continuously superfused with extracellular saline.

Force-Indentation measurements: The measurements were performed with the FALCON system described in Eastwood et al, 2015. In brief, we used piezoresistive cantilevers to deform the worm’s cuticle and to read out the respected indentation and force. Measurements were performed in displacement clamp. The cantilever had a spring constant kc of 1.3 N/m and a resonant frequency of 12.2 kHz. A glass microsphere (10 ± 1-μm diameter) was adhered to the cantilever tip. Cantilevers were mounted to a piezoelectric actuator. Because the device was placed directly above the worm’s surface before each experiment, sample indentation depth (z) was calculated as z = xt – xc,where xt is the total actuator displacement as measured by the built-in sensor on the actuator and xc is the cantilever deflection as measured by the piezoresistor, as described (Park et al., 2007; Eastwood et al., 2015). Force was calculated as F= xt*kc. For each animal, we applied 15 displacement steps (0.5 – 12.5µm) in three replicates. The cantilever was positioned 154 ± 37 μm behind the pharynx. Data acquisition occurred with HEKA software and a sampling frequency of 10 kHz. Analysis was performed in Matlab.

Reagents

CB128: dpy-10(e128); N2. Strains available at the CGC.
Extracellular saline: in mM: NaCl (145), KCl (5), MgCl2 (5), CaCl2 (1), Hepes (10), adjusted to pH 7.2 with NaOH. 8% agarose (wt/vol) dissolved in extracellular saline, pH adjusted to 8.01 with NaOH.

References

Levy, A.D., Yang, J., & Kramer, J.M. 1993. Molecular and genetic analyses of the Caenorhabditis elegans dpy-2 and dpy-10 collagen genes: a variety of molecular alterations affect organismal morphology. Mol. Biol. Cell., 4, 803-17.
PubMed
Park, S.J., Goodman, M.B. and Pruitt, B.L. 2007. Analysis of nematode mechanics by piezoresistive displacement clamp. Proc Natl Acad Sci USA, 104, 17376–17381.
10.1073/pnas.0702138104 | PubMed
Wheeler J.M., Thomas J.H. 2006. Identification of a novel gene family involved in osmotic stress response in Caenorhabditis elegans. Genetics, 174:1327–1336.
10.1534/genetics.106.059089 | PubMed
Eastwood, A.L., Sanzeni, A., Petzold, B. C., Park, S., Vergassola, M., Pruitt, B. L., & Goodman, M.B. 2015. Tissue mechanics govern the rapidly adapting and symmetrical response to touch. Proc Natl Acad Sci USA, 112, E6955-63.
10.1073/pnas.1514138112 | PubMed

Funding

German Research Foundation (DFG, 313913559) (SF), R01NS047715 (MBG), R01EB006745 (MBG, BLP), R35NS129879 (MBG), SNSF (FL), F31NS100318 (ALN).

Reviewed By

Anonymous

History

Received: August 1, 2018
Accepted: August 3, 2018
Published: August 6, 2018

Copyright

© 2018 by the authors. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Fechner, S; Loizeau, F; Nekimken, AL; Pruitt, BL; Goodman, MB (2018). The bodies of dpy-10(e128) are twice as stiff as wild type. microPublication Biology. 10.17912/ecsm-mp67.
Download: RIS BibTeX
microPublication Biology is published by
1200 E. California Blvd. MC 1-43 Pasadena, CA 91125
The microPublication project is supported by
The National Institute of Health -- Grant #: 1U01LM012672-01
microPublication Biology:ISSN: 2578-9430