4.4 Article

Determination of the lowest concentrations of aldehyde fixatives for completely fixing various cellular structures by real-time imaging and quantification

Journal

HISTOCHEMISTRY AND CELL BIOLOGY
Volume 139, Issue 5, Pages 735-749

Publisher

SPRINGER
DOI: 10.1007/s00418-012-1058-5

Keywords

Aldehyde fixatives; Glutaraldehyde; Formaldehyde; Paraformaldehyde; Human umbilical vein endothelial cells (HUVECs); Cell fixation; Cell blebbing

Funding

  1. National Natural Science Foundation of China [30900340]
  2. Natural Science Foundation of Jiangxi Province [2010GZN0138]
  3. Scientific Research Foundation for Returned Overseas Chinese Scholar of State Education Ministry
  4. Scientific Research Fund of Jiangxi Provincial Education Department [GJJ10305]

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The effectiveness of fixatives for fixing biological specimens has long been widely investigated. However, the lowest concentrations of fixatives needed to completely fix whole cells or various cellular structures remain unclear. Using real-time imaging and quantification, we determined the lowest concentrations of glutaraldehyde (0.001-0.005, similar to 0.005, 0.01-005, 0.01-005, and 0.01-0.1 %) and formaldehyde/paraformaldehyde (0.01-0.05, similar to 0.05, 0.5-1, 1-1.5, and 0.5-1 %) required to completely fix focal adhesions, cell-surface particles, stress fibers, the cell cortex, and the inner structures of human umbilical vein endothelial cells within 20 min. With prolonged fixation times (> 20 min), the concentration of fixative required to completely fix these structures will shift to even lower values. These data may help us understand and optimize fixation protocols and understand the potential effects of the small quantities of endogenously generated aldehydes in human cells. We also determined the lowest concentration of glutaraldehyde (0.5 %) and formaldehyde/paraformaldehyde (2 %) required to induce cell blebbing. We found that the average number and size of the fixation-induced blebs per cell were dependent on both fixative concentration and cell spread area, but were independent of temperature. These data provide important information for understanding cell blebbing, and may help optimize the vesiculation-based technique used to isolate plasma membrane by suggesting ways of controlling the number or size of fixation-induced cell blebs.

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