Caspase inhibitor Z-VAD-FMK enhances the freeze-thaw survival rate of human embryonic stem cells

被引:42
作者
Heng, Boon Chin
Clement, Marie Veronique
Cao, Tong
机构
[1] Natl Univ Singapore, Fac Dent, Stem Cell Lab, Singapore 119074, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117597, Singapore
基金
美国国家卫生研究院;
关键词
apoptosis; cryopreservation; embryonic; freezing; human; inhibition; stem cells;
D O I
10.1007/s10540-007-9051-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previous study demonstrated that the low survival of human embryonic stem cells (hESC) under conventional slow-cooling cryopreservation protocols is predominantly due to apoptosis rather than cellular necrosis. Hence, this study investigated whether a synthetic broad-spectrum irreversible inhibitor of caspase enzymes, Z-VAD-FMK can be used to enhance the post-thaw survival rate of hESC. About 100 mM Z-VAD-FMK was supplemented into either the freezing solution, the post-thaw culture media or both. Intact and adherent hESC colonies were cryopreserved so as to enable subsequent quantitation of the post-thaw cell survival rate through the MTT assay, which can only be performed with adherent cells. Exposure to 100 mM Z-VAD-FMK in the freezing solution alone did not significantly enhance the post-thaw survival rate (10.2% vs. 9.9%, p > 0.05). However, when 100 mM Z-VAD-FMK was added to the post-thaw culture media, there was a significant enhancement in the survival rate from 9.9% to 14.4% (p < 0.05), which was further increased to 18.7% when Z-VAD-FMK was also added to the freezing solution as well (p < 0.01). Spontaneous differentiation of hESC after cryopreservation was assessed by morphological observations under bright-field microscopy, and by immunocytochemical staining for the pluripotency markers SSEA-3 and TRA-1-81. The results demonstrated that exposure to Z-VAD-FMK did not significantly enhance the spontaneous differentiation of hESC within post-thaw culture.
引用
收藏
页码:257 / 264
页数:8
相关论文
共 20 条
[1]   Successful production of blastocysts following ultrarapid vitrification with step-wise equilibriation of germinal VesicleStage mouse oocytes [J].
Aono, N ;
Naganuma, T ;
Abe, Y ;
Hara, K ;
Sasada, H ;
Sato, E ;
Yoshida, H .
JOURNAL OF REPRODUCTION AND DEVELOPMENT, 2003, 49 (06) :501-506
[2]  
Baust JM, 2000, IN VITRO CELL DEV-AN, V36, P262
[3]   Mouse and human embryonic stem cell models of hematopoiesis: past, present, and future [J].
Chen, D ;
Lewis, RL ;
Kaufman, DS .
BIOTECHNIQUES, 2003, 35 (06) :1253-+
[4]   High survival rate of bovine oocytes matured in vitro following vitrification [J].
Chian, RC ;
Kuwayama, M ;
Tan, L ;
Tan, J ;
Kato, O ;
Nagai, T .
JOURNAL OF REPRODUCTION AND DEVELOPMENT, 2004, 50 (06) :685-696
[5]   Stem cells and the formation of the myocardium in the vertebrate embryo [J].
Eisenberg, LM ;
Kubalak, SW ;
Eisenberg, CA .
ANATOMICAL RECORD PART A-DISCOVERIES IN MOLECULAR CELLULAR AND EVOLUTIONARY BIOLOGY, 2004, 276A (01) :2-12
[6]   Low O2 tensions and the prevention of differentiation of hES cells [J].
Ezashi, T ;
Das, P ;
Roberts, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (13) :4783-4788
[7]   Inhibition of human caspases by peptide-based and macromolecular inhibitors [J].
Garcia-Calvo, M ;
Peterson, EP ;
Leiting, B ;
Ruel, R ;
Nicholson, DW ;
Thornberry, NA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (49) :32608-32613
[8]   Cell therapy using human embryonic stem cells [J].
Gerecht-Nir, S ;
Itskovitz-Eldor, J .
TRANSPLANT IMMUNOLOGY, 2004, 12 (3-4) :203-209
[9]  
Gribaldo Laura, 2002, Experimental Hematology (Charlottesville), V30, P628, DOI 10.1016/S0301-472X(02)00827-5
[10]  
Heng BC, 2005, BIOTECHNOL APPL BIOC, V41, P97