科研之友
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摘要
Cryopreservation of specimens taken from the genital tract of women is important for studying mucosa] immunity during HIV prevention trials. However, it is unclear whether the current, empirically developed cryopreservation procedures for peripheral blood cells are also ideal for genital specimens. The optimal cryopreservation protocol depends on the cryobiological features of the cells. Thus, we obtained tissue specimens from vaginal repair surgeries, isolated and flow cytometry-purified immune cells, and determined fundamental cryobiological characteristics of vaginal CD3(+) T cells and CD14(+) macrophages using a microfluidic device. The osmotically inactive volumes of the two cell types (V-b) were determined relative to the initial cell volume (V-0) by exposing the cells to hypotonic and hypertonic saline solutions, evaluating the equilibrium volume, and applying the Boyle van't Hoff relationship. The cell membrane permeability to water (L-p) and to four different cryoprotective agent (CPA) solutions (P-s) at room temperature were also measured. Results indicated V-b values of 0.516 V-0 and 0.457 V-0 for mucosa] T cells and macrophages, respectively. L-p values at room temperature were 0.196 and 0.295 pm/miniatm for T cells and macrophages, respectively. Both cell types had high P-s values for the three CPAs, dimethyl sulfoxide (DMSO), propylene glycol (PG) and ethylene glycol (EG) (minimum of 0.418 x 10(-3) cm/min), but transport of the fourth CPA, glycerol, occurred 50-150 times more slowly. Thus, DMSO, PG, and EG are better options than glycerol in avoiding severe cell volume excursion and osmotic injury during CPA addition and removal for cryopreservation of human vaginal immune cells. Published by Elsevier Inc. This is an open access article under the CC BY license.
