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Postnatal extra-embryonic tissues as a source of multiple cell types for regenerative medicine applications
Summary. Aim: We aimed to isolate and characterize the cell types which could be obtained from postnatal extra-embryonic tissues. Materials and Methods: Fresh tissues (no more than 12 h after delivery) were used for enzymatic or explants methods of cell isolation. Obtained cultures were further maintained at 5% oxygen. At P3 cell phenotype was assessed by fluorescence-activated cell sorting, population doubling time was calculated and the multilineage differentiation assay was performed. Results: We have isolated multiple cell types from postnatal tissues. Namely, placental mesenchymal stromal cells from placenta chorionic disc, chorionic membrane mesenchymal stromal cells (ChM-MSC) from free chorionic membrane, umbilical cord MSC (UC-MSC) from whole umbilical cord, human umbilical vein endothelial cells (HUVEC) from umbilical vein, amniotic epithelial cells (AEC) and amniotic MSC (AMSC) from amniotic membrane. All isolated cell types displayed high proliferation rate together with the typical MSC phenotype: CD73+CD90+CD105+CD146+CD166+CD34-CD45-HLA-DR-. HUVEC constitutively expressed key markers CD31 and CD309. Most MSC and AEC were capable of osteogenic and adipogenic differentiation. Conclusion: We have shown that a wide variety of cell types can be easily isolated from extra-embryonic tissues and expanded ex vivo for regenerative medicine applications. These cells possess typical MSC properties and can be considered an alternative for adult MSC obtained from bone marrow or fat, especially for allogeneic use.
Submitted: August 4, 2017.
*Correspondence: E-mail: firstname.lastname@example.org
Abbreviations used: AEC — amniotic epithelial cells; AMSC — amniotic MSC; ChM-MSC — chorionic membrane MSC; EMT — epithelial-mesenchymal transition; FACS — fluorescence-activated cell sorting; HUVEC — human umbilical vein endothelial cells; MSC — mesenchymal stromal/stem cells; PDT — population doubling time; Pl-MSC — placental MSC; UC-MSC enz. — umbilical cord MSC isolated by enzymatic digestion; UC-MSC expl. — umbilical cord MSC isolated by explants method.
Extra-embryonic tissues are composed of the placenta, fetal membranes, and umbilical cord. The placenta is a disc with a diameter of 15–20 cm and a thickness of 2–3 cm. The fetal membranes, amnion and chorion, extend from the edges of the chorionic disc and enclose the amniotic fluid and the fetus. Placenta, amnion and umbilical cord are usually discarded after childbirth whereas they are a reserve of a variety of cell types. During last years these postnatal extra-embryonic tissues have attracted much attention as a valuable source of stem cells to be used in medicine as they are readily available, and their potential use for cell therapy poses no ethical issues. Moreover, due to their early embryonic origin, extra-embryo stem cells have more plasticity comparing to adult stem cells and additionally possess immunomodulatory potential (as a part of fetomaternal tolerance mechanism), which allows their safe use even in allogeneic applications . Thus we were interested in characterization and comparison of the maximal quantity of cell types which could be isolated from term extra-embryo tissues.
MATERIALS AND METHODS
Our experiments were done in accordance with the bioethics and biological safety norms confirmed by the Medical company ilaya® Bioethics Commission permission. All donors have signed an informed consent before tissue donation.
Cell isolation and culturing. Fresh afterbirth (less than 12 h after delivery) was disassembled to different tissue types and washed several times in HBSS (Sigma-Aldrich, USA) with 1 g/l streptomycin, 1000,000 IU/l penicillin and 2.5 mg/ml amphotericin B (Sigma-Aldrich, USA). Mesenchymal stromal cells (MSC) of different origin were isolated by explants method or via enzymatic digestion. Respective tissues were minced and digested in a mix of 0.1% pronase and 0.1% collagenase type II in DMEM/F12 medium supplemented with 2% FBS (all from Sigma-Aldrich, USA) for 1 h at +37 °C. The reaction mix was then diluted 5× with PBS (Sigma-Aldrich, USA) and the cells were pelleted at 800 g 10 min at +4 °C. Afterwards the cells were resuspended in growth medium (α-MEM supplemented with 10% FBS, 1 ng/ml bFGF (all from Sigma-Aldrich, USA), 200 μM stable L-glutamine, 1× antibiotic-antimycotic solution (all from BioWest, France) and further cultured at +37 °C, 5% O2 and 5% CO2 in a multigas incubator (Binder CB 210, Germany).
Human umbilical vein endothelial cells (HUVEC) were obtained by a brief digestion of the inner wall of umbilical vein by 0.1% collagenase type II in DMEM/F12 medium (Sigma-Aldrich, USA). The cells were further cultured on collagen-coated dishes in EGM-2 medium (Lonza, USA) at +37 °C, 5% O2 and 5% CO2 in a multigas incubator (Binder CB 210, Germany).
Amniotic epithelial cells (AEC) were isolated as described by Miki et al. . Briefly, the amnion was separated from the chorion, extensively washed in PBS (Sigma-Aldrich, USA) until no blood clots remained. Then the tissue was briefly washed in PBS with 0.53 mM Na2EDTA and digested twice in 0.05% trypsin in 0.53 mM Na2EDTA (Sigma-Aldrich, USA) for 40 min at +37 °C. Each time the reaction was stopped with double volume of α-MEM supplemented with 10% FBS (Sigma-Aldrich, USA). The cells were pelleted at 400 g 10 min at +4 °C. The cell viability was assessed by Trypan Blue staining (Sigma-Aldrich, USA). Then up to 105 cells/cm2 were seeded on collagen-coated dishes. The cells were cultured in DMEM/F12 medium supplemented with 10% FBS, 10 ng/ml EGF, 1 ng/ml bFGF, 1× sodium pyruvate, 100 μM isoproterenol (all from Sigma-Aldrich, USA), 200 μM stable L-glutamine, 1× antibiotic-antimycotic (all from BioWest, France) at +37 °C, 5% O2 and 5% CO2 in a multigas incubator (Binder CB 210, Germany).
Amniotic MSC (AMSC) were isolated by explants method from the remains of amniotic membrane trypsin digestion.
The cells were subcultured when they reached about 90% confluency. 0.05% trypsin in 0.53 mM Na2EDTA (Sigma Aldrich, USA) was used for cell dissociation.
The population doubling time (PDT) was calculated using the online source: http://www.doubling-time.com/compute.php .
Flow cytometry. The cell phenotype was assessed by fluorescence-activated cell sorting (FACS) on the BD FACSAria flow cytometer (BD Pharmingen, BD Horizon, USA). Staining with the monoclonal antibodies (PerCP-Cy5.5 mouse anti-human CD105, APC mouse anti-human CD73, FITC mouse anti-human CD90, PE-Cy5 mouse anti-human HLA-DR, PE-Cy7 mouse anti-human CD31, APC mouse anti-human CD34, FITC mouse anti-human CD45, PE-CF592 mouse anti-human CD146, BV421 mouse anti-human CD166, PF mouse anti-human CD309) was performed according to the manufacturer’s instructions (BD Pharmingen, BD Horizon, USA).
Directed multilineage differentiation. Adipogenic and osteogenic differentiation were performed as described previously . Briefly, adipogenic differentiation was performed in DMEM with high glucose content (4.5 g/l) (Sigma-Aldrich, USA) supplemented with 5% horse serum (BioWest, France), 10% FBS, 1 µM dexamethasone, 200 µM indomethacine, 500 µM isobutylmethylxanthine and 5 µg/ml insulin (all from Sigma-Aldrich, USA). After 14 days the cells were fixed and stained with Oil Red O (Sigma-Aldrich, USA).
Osteogenic differentiation was performed in DMEM with low glucose content (1 g/l) with 10% FBS, 100 nM dexamethasone, 10 mM b-glycerophosphate and 50 µg/ml ascorbate-2-phosphate (all from Sigma-Aldrich, USA). After 14 or 21 days the cells were fixed and stained with BCIP/NBT Liquid Substrate System or Alizarin Red S respectively (all from Sigma-Aldrich, USA).
RESULTS AND DISCUSSION
Extra-embryonic tissues-derived cells possess MSC phenotype. Overall we obtained seven cell culture types from extra-embryonic tissues. We used enzymatic digestion to isolate cells from placenta (further referred as placental mesenchymal stromal cells — Pl-MSC), from free chorionic membrane (ChM-MSC), from amniotic membrane (AEC), two cell types from umbilical cord (MSC isolated by enzymatic digestion — UC-MSC enz. and HUVEC). Two more cell types were obtained by explants method: from amniotic membrane (AMSC) and from umbilical cord (UC-MSC expl.). The cells phenotype was assessed by FACS at P3. All described cell types demonstrated high level of MSC markers expression, e.g. CD73, CD90, CD105, CD146, CD166 (except HUVEC which did not express CD90); and did not express markers of hematopoietic progenitor cells, e.g. CD34, CD45, HLA-DR (Table, Fig. 1). HUVEC additionally expressed key markers CD31 and CD309. Interestingly, AEC maintained the same level of MSC markers expression until P8 (data not shown).
Table. Flow cytometry results of surface antigen expression on extra-embryonic tissues-derived cells. Data presented as a percentage of parent population
Note: N/D — not determined.
Fig. 1. Representative FACS graphics (for HUVEC)
PDT and morphology of extra-embryonic tissues-derived cells. Along with the phenotype analysis we calculated the PDT at P1–P3 for all described cell lines. The average PDT for most cell lines was about 30 h (Fig. 2). However, AEC and UC-MSC enz. doubled their number in less than 24 h, whereas the PDT for HUVEC was about 60 h. On the whole, extra-embryonic tissues-derived cell lines demonstrated high proliferation potential with stable PDT for at least three passages.
Fig. 2. PDT of extra-embryonic tissues-derived cells
As expected, HUVEC had epitheloid morphology, whereas all other cell lines demonstrated typical for MSC fibroblastoid morphology (Fig. 3, a–f). Interestingly, AEC, initially possessing typical epitheloid morphology, progressively acquired fibroblastoid appearance at P2–P3 (Fig. 3, g) probably due to the EMT .
Fig. 3. Morphology of extra-embryonic tissues-derived cells. The photos are taken at P1. Phase-contrast microscopy. The bar = 200 μm. a — AMSC; b — ChM-MSC; c — Pl-MSC; d — UC-MSC enz.; e — UC-MSC expl.; f — HUVEC; g — epithelial-to-mesenchymal change of AEC morphology in culture. The passages are indicated in image corners
Multilineage differentiation of extra-embryonic tissues-derived cells. Next, we performed adipogenic and osteogenic differentiation to assess cell plasticity of all MSC cell lines and AEC. All described cell types successfully underwent adipogenic differentiation. However, it was atypical (comparing to “classic” bone marrow MSC ) as there was plenty of tiny lipid vacuoles instead of several big vesicles (Fig. 4, a–f). Also AEC and most MSC cells were capable of osteogenic differentiation (assessed by alkaline phosphatase activity at early stages or by Alizarin Red S staining at final stages). The only exceptions were the Pl-MSC and UC-MSC enz. that failed typical osteogenic differentiation. Instead Pl-MSC formed spheres. Surprisingly, UC-MSC isolated via explants qualitatively demonstrated osteogenic differentiation. However, previous studies demonstrate that UC-MSC osteogenic differentiation is quite problematic and depends on multiple factors, e.g. culture conditions and even which UC segment they are isolated from [7, 8]. Probably, isolation via explants favors UC-MSC capability of mesenchymal lineage differentiation.
Fig. 4. Multilineage differentiation of extra-embryonic tissues-derived cells. (a–f) Adipogenic differentiation. Red Oil O and Romanowsky stains. Phase-contrast microscopy. The bar = 50 μm. a — AEC; b — AMSC; c — ChM-MSC; d — Pl-MSC; e — UC-MSC enz.; f — UC-MSC expl. (g–i) Osteogenic differentiation. BCIP/NBT stain. Light microscopy. The bar = 100 μm. g — AEC; h — ChM-MSC; i — Pl-MSC. (j–l) Osteogenic differentiation. Alizarin Red S stain. Phase-contrast microscopy. The bar = 100 μm. j — AMSC; k — UC-MSC enz.; l — UC-MSC expl.
Thus obtained MSC cultures fulfill mostly all minimal MSC criteria , e.g. adherence to plastic, expression of typical MSC markers (CD73+,CD90+,CD105+ and others) and multilineage differentiation. Moreover, they demonstrate high and stable proliferation rate thereby allowing obtaining a therapeutic dose in a short time. Their usage is not restricted by any ethical issues, and due to their immunophenotype (CD34-CD45-HLA-DR-) they could be safely used for allogeneic applications. Two special cell types are of particular interest as they have unique properties: HUVEC and AEC. HUVEC as effective angiogenic progenitors may be used for regeneration of vessels or vascularization of complex organ transplants as well as for separate applications for correction of the tissue ischemic consequences . As for AEC, they originate from embryonic epiblast, thereby capable of generating cells from all three germ layers (ectoderm, mesoderm and endoderm) . This is of particular interest as it potentially permits liver and pancreas restoration. Moreover, several successive animal studies have already been performed in those directions [11, 12]. These outstanding features together with high accessibility make multiple cell types isolated from extra-embryonic tissues an attractive substrate for regenerative medicine applications.
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