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Beneficial effect of intracellular trehalose on the membrane integrity of dried mammalian cells

  • Tani Chen(corresponding author)
    ,
  • Jason P. Acker
    ,
  • ,
  • Stephen Cheley
    ,
  • Hagan Bayley
    ,
  • Alex Fowler
*Corresponding author for this work
  • Harvard University
    ,
  • Texas A&M University
    ,
  • University of Massachusetts Dartmouth
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Recently, there has been much interest in using trehalose and other small carbohydrates to preserve mammalian cells in the dried state as an alternative to cryopreservation. Here, we report on the successful preservation of plasma membrane integrity after drying, as a first step toward full preservation of mammalian cells. Trehalose was introduced into cells using a genetically engineered version of α-hemolysin, a pore-forming protein; the cells were then dried and stored for weeks at different temperatures with ∼90% recovery of the intact plasma membrane. We show that protection of the plasma membrane by internal trehalose is dose dependent and estimate the amount of internal trehalose required for adequate protection to be ∼1010 molecules/cell. In addition, a minimal amount of water (∼15 wt%) appears to be necessary. These results show that a key component of mammalian cells can be preserved in a dried state for weeks under mild conditions (-20°C and 5% relative humidity) and thereby suggest new approaches to preserving mammalian cells.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 168-181 (14 pages)

Journal (Volume, Issue Number)

Cryobiology (Volume 43, Issue 2)

Publication milestones

  • Published - 09/2001

Publication status

Published - 09/2001

ISSN

0011-2240

Publication IDs

  • Scopus: 0036185789
  • PubMed: 11846471

Publication metrics

Metrics

SciVal
citations
151
Fractional count
1
Fractional count
0.14
Fractional count
6
Fractional count
0.86
Fractional count
1
Fractional count
1
SciVal
FWCI
4.72
SciVal
Author count
7
SciVal
Paper percentile
96
SciVal
Top percentile
5
Scopus
citations

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Captures
104
Citation count
167

Funding Details

This work was partially supported by the NIH (Grant DK46270) and the Shriners Hospitals for Children. J.P.A. was supported by a Post-Doctoral Fellowship from the Canadian Institutes of Health Research.
FundersFunding number
NIH
-
NIDDK
R01DK046270
Shriners Hospitals for Children
-
CIHR
-