Abstract
Here, we describe methods of transmission electron microscopy (TEM) based on conventional chemical fixation and high-pressure freezing (HPF) and freeze-substitution (FS) to examine the ultrastructure of Arabidopsis pollen grains and pollen tubes. Compared to other plant samples, such as root or leaf, pollen grains have thick pollen coat and cell wall which limit the permeation of fixative. Thus, it is difficult to obtain high-quality ultrastructural images of pollen. Moreover, pollen tube is very soft and the traditional procedure is too harsh to get an intact pollen tube sample. Up to now, there is no available mature protocol for TEM sample preparation of Arabidopsis pollen tube. Here, we describe the details and step-by-step procedures of chemical fixation, HPF, FS, and resin-embedding protocols for Arabidopsis pollen and pollen tube. In addition, we also provide a method on how to get longitudinal sections of pollen tubes.
Key words
- Pollen
- Pollen tube
- Transmission electron microscopy
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References
Kang BH (2010) Electron microscopy and high-pressure freezing of Arabidopsis. Methods Cell Biol 96:259–283
Luft JH (1961) Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol 9:409–414
Acknowledgment
This work is supported by the grant from National Natural Science Foundation of China (31571385 and 31330053).
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Jia, PF., Li, HJ., Yang, WC. (2017). Transmission Electron Microscopy (TEM) to Study Histology of Pollen and Pollen Tubes. In: Schmidt, A. (eds) Plant Germline Development. Methods in Molecular Biology, vol 1669. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7286-9_15
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DOI: https://doi.org/10.1007/978-1-4939-7286-9_15
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Publisher Name: Humana Press, New York, NY
Print ISBN: 978-1-4939-7285-2
Online ISBN: 978-1-4939-7286-9
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