User:Daniel Mietchen/Notebook/Open Science/Wiki journal/Demo: Difference between revisions
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Authors: [[User:AuthorID_of_Daniel Mietchen|Daniel Mietchen]], [[User:AuthorID_of_Bertram Manz|Bertram Manz]], [[User:AuthorID_of_Frank Volke|Frank Volke]], [[User:AuthorID_of_Kenneth B. Storey|Kenneth Storey]] | Authors: [[User:AuthorID_of_Daniel Mietchen|Daniel Mietchen]], [[User:AuthorID_of_Bertram Manz|Bertram Manz]], [[User:AuthorID_of_Frank Volke|Frank Volke]], [[User:AuthorID_of_Kenneth B. Storey|Kenneth Storey]] | ||
==Abstract== | ==Abstract== | ||
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Temperatures below the [[freezing point of water]] and the ensuing [[ice crystal formation]] pose serious challenges to [[cell structure]] and [[cell function|function]]. Consequently, [[species (biology)|species]] living in [[seasonally cold environment]]s have [[evolution (biology)|evolved]] a multitude of strategies to reorganize their [[cellular architecture]] and [[cell metabolism|metabolism]], and the underlying mechanisms are crucial to our understanding of [[life (biology)|life]]. In [[multicellular organism]]s, and [[poikilotherm animal]]s in particular, our knowledge about these processes is almost exclusively due to [[invasive study|invasive studies]], thereby limiting the range of conclusions that can be drawn about intact living systems. | Temperatures below the [[freezing point of water]] and the ensuing [[ice crystal formation]] pose serious challenges to [[cell structure]] and [[cell function|function]]. Consequently, [[species (biology)|species]] living in [[seasonally cold environment]]s have [[evolution (biology)|evolved]] a multitude of strategies to reorganize their [[cellular architecture]] and [[cell metabolism|metabolism]], and the underlying mechanisms are crucial to our understanding of [[life (biology)|life]]. In [[multicellular organism]]s, and [[poikilotherm animal]]s in particular, our knowledge about these processes is almost exclusively due to [[invasive study|invasive studies]], thereby limiting the range of conclusions that can be drawn about intact living systems. | ||
===Methodology=== | ===Methodology=== | ||
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[[CHESS imaging]] has previously been used to investigate insect larval development in a non-cryobiological context, and technological developments in the MR field have recently seen in vivo spatial resolution in non-frozen samples reach the size range relevant for entomological and subcellular investigations. | [[CHESS imaging]] has previously been used to investigate insect larval development in a non-cryobiological context, and technological developments in the MR field have recently seen in vivo spatial resolution in non-frozen samples reach the size range relevant for entomological and subcellular investigations. | ||
The present study combined these two fields of investigation by demonstrating the feasibility of high-resolution MR imaging of insect larvae in a cryobiological context. | The present study combined these two fields of investigation by demonstrating the feasibility of high-resolution MR imaging of insect larvae in a cryobiological context. | ||
===Results=== | ===Results=== | ||
In vivo MR images were acquired from autumn-collected larvae at temperatures between 0°C and about −70°C and at [[spatial resolution]]s down to 27 µm. These images revealed three-dimensional (3D) larval anatomy at a level of detail currently not in reach of other in vivo techniques. Furthermore, they allowed visualization of the 3D distribution of the remaining [[liquid water]] and of the [[endogenous cryoprotectant]]s at subzero temperatures, and [[Temperature-weighted imaging|temperature-weighted images]] of these distributions could be derived. Finally, individual [[fat body (insects)|fat body]] cells and their [[nucleus (cell)|nuclei]] could be identified in intact frozen Eurosta larvae. | In vivo MR images were acquired from autumn-collected larvae at temperatures between 0°C and about −70°C and at [[spatial resolution]]s down to 27 µm. These images revealed three-dimensional (3D) larval anatomy at a level of detail currently not in reach of other in vivo techniques. Furthermore, they allowed visualization of the 3D distribution of the remaining [[liquid water]] and of the [[endogenous cryoprotectant]]s at subzero temperatures, and [[Temperature-weighted imaging|temperature-weighted images]] of these distributions could be derived. Finally, individual [[fat body (insects)|fat body]] cells and their [[nucleus (cell)|nuclei]] could be identified in intact frozen Eurosta larvae. | ||
===Conclusions=== | ===Conclusions=== | ||
Revision as of 04:09, 10 February 2010
In Vivo Assessment of Cold Adaptation in Insect Larvae by Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy
Authors: Daniel Mietchen, Bertram Manz, Frank Volke, Kenneth Storey
Abstract
Background
Temperatures below the freezing point of water and the ensuing ice crystal formation pose serious challenges to cell structure and function. Consequently, species living in seasonally cold environments have evolved a multitude of strategies to reorganize their cellular architecture and metabolism, and the underlying mechanisms are crucial to our understanding of life. In multicellular organisms, and poikilotherm animals in particular, our knowledge about these processes is almost exclusively due to invasive studies, thereby limiting the range of conclusions that can be drawn about intact living systems.
Methodology
Given that non-destructive techniques like 1H MR imaging and spectroscopy exhibit an enormous signal loss upon freezing and a corresponding signal increase upon thawing and have proven useful for in vivo investigations of a wide range of biological systems, we aimed at evaluating their potential to observe cold adaptations in living insect larvae. Specifically, we chose two cold-hardy insect species that frequently serve as cryobiological model systems and share the same habitat (stem galls on goldenrod plants, genus Solidago) but use different overwintering strategies–the freeze-avoiding gall moth Epiblema scudderiana and the freeze-tolerant gall fly Eurosta solidaginis.
CHESS imaging has previously been used to investigate insect larval development in a non-cryobiological context, and technological developments in the MR field have recently seen in vivo spatial resolution in non-frozen samples reach the size range relevant for entomological and subcellular investigations. The present study combined these two fields of investigation by demonstrating the feasibility of high-resolution MR imaging of insect larvae in a cryobiological context.
Results
In vivo MR images were acquired from autumn-collected larvae at temperatures between 0°C and about −70°C and at spatial resolutions down to 27 µm. These images revealed three-dimensional (3D) larval anatomy at a level of detail currently not in reach of other in vivo techniques. Furthermore, they allowed visualization of the 3D distribution of the remaining liquid water and of the endogenous cryoprotectants at subzero temperatures, and temperature-weighted images of these distributions could be derived. Finally, individual fat body cells and their nuclei could be identified in intact frozen Eurosta larvae.
Conclusions
These findings suggest that high resolution MR techniques provide for interesting methodological options in comparative cryobiological investigations, especially in vivo.
Citation: Mietchen D, Manz B, Volke F, Storey K (2008) In Vivo Assessment of Cold Adaptation in Insect Larvae by Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy. PLoS ONE 3(12): e3826. doi:10.1371/journal.pone.0003826
Editor: Brent Sinclair
Funding: The study was supported by an IBMT-internal grant. Competing interests: The authors have declared that no competing interests exist.
