Directed Differentiation of Hemogenic Endothelial Cells from Human Pluripotent Stem Cells

摘要

Presented here is a simple protocol for the directed differentiation of hemogenic endothelial cells from human pluripotent stem cells in approximately 1 week.

摘要

Blood vessels are ubiquitously distributed within all tissues of the body and perform diverse functions. Thus, derivation of mature vascular endothelial cells, which line blood vessel lumens, from human pluripotent stem cells is crucial for a multitude of tissue engineering and regeneration applications. In vivo, primordial endothelial cells are derived from the mesodermal lineage and are specified toward specific subtypes, including arterial, venous, capillary, hemogenic, and lymphatic. Hemogenic endothelial cells are of particular interest because, during development, they give rise to hematopoietic stem and progenitor cells, which then generate all blood lineages throughout life. Thus, creating a system to generate hemogenic endothelial cells in vitro would provide an opportunity to study endothelial-to-hematopoietic transition, and may lead to ex vivo production of human blood products and reduced reliance on human donors. While several protocols exist for the derivation of progenitor and primordial endothelial cells, generation of well-characterized hemogenic endothelial cells from human stem cells has not been described. Here, a method for the derivation of hemogenic endothelial cells from human embryonic stem cells in approximately 1 week is presented: a differentiation protocol with primitive streak cells formed in response to GSK3β inhibitor (CHIR99021), then mesoderm lineage induction mediated by bFGF, followed by primordial endothelial cell development promoted by BMP4 and VEGF-A, and finally hemogenic endothelial cell specification induced by retinoic acid. This protocol yields a well-defined population of hemogenic endothelial cells that can be used to further understand their molecular regulation and endothelial-to-hematopoietic transition, which has the potential to be applied to downstream therapeutic applications.

引言

Endothelial cells (ECs) are a heterogeneous population of cells that perform multiple functions throughout the human body and in engineered tissues. In addition to supporting and regulating other cell types (i.e., cardiomyocytes¹, osteoblastic cells²), these functions include forming a selective barrier between blood and tissues and assisting in tissue formation³. Differentiation of mature ECs during normal development requires diverse signaling pathways. Primordial ECs are derived from mesoderm progenitors, and are then specified toward mature arterial, venous, capillary and lymphatic phenotypes⁴. Additionally, a small subset of ECs in the extraembryonic yolk sac and embryonic Aorta-Gonad-Mesonephros (AGM) region are also specified to become hemogenic ECs, which give rise to hematopoietic stem and progenitor cells (HSPCs) that migrate to the fetal liver and fetal bone marrow, where they remain postnatally and generate all blood cell types throughout life⁴. The diverse range of EC phenotypes is essential for all tissue development and maintenance.

Thus, ECs and their derivatives are critical components of studies aimed at modeling, and elucidating mechanisms of, human development and/or disease, as well as regenerative medicine and tissue engineering applications^5,6,7,8. However, the main limitation for these types of studies is the lack of availability of primary human ECs in the quantity required. It has been estimated that a minimum of 3 x 10⁸ ECs would be required for the majority of therapeutic applications⁶. To solve this problem, the use of human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs) has been proposed due to their diverse lineage potential and their ability to generate large numbers of progeny^6,9.

Indeed, the usefulness of cells derived from hESCs or hiPSCs has been demonstrated in multiple studies focused on disease modeling and drug screening^10,11,12. Organ-on-a-Chip (OOC) technology has been used to more faithfully recapitulate the physiology of the human body by integrating cells and tissues into three-dimensional scaffolds. Furthermore, connection of multiple individual OOCs (a so-called body- or human-on-a-chip, BOC/HOC) can be accomplished via microfluidics to allow for crosstalk between the organs of interest^13,14,15. Supporting tissues, such as the vasculature, are critical components of OOCs and BOC/HOCs; incorporating vasculature allows for the transport of nutrients, oxygen, and paracrine factors throughout the tissues, thereby promoting the requisite tissue-specific microenvironment^3,12. Thus, methods for deriving mature human ECs, such as arterial, venous, lymphatic, and hemogenic ECs, are crucial to advancing these tissue engineering approaches.

Multiple protocols have been published detailing steps for the derivation of human primordial or progenitor ECs from hESCs or hiPSCs^{5,16,17,18,19,20,21,22,23,24,25,26}. Many of these protocols rely on embryoid body (EB) formation or co-culture of ESCs/iPSCs with a murine feeder layer of stromal cells. These strategies tend to be difficult and time consuming, with low EC yields and/or contamination of human ECs with murine cells. Protocols that rely strictly on 2D culture without the use of stromal cells often require long inductions, utilize complex combinations of growth factors and/or inhibitors for induction, have extended expansion periods following cell separation, or a combination of these factors. Advancing knowledge of signaling pathways and factors involved in the derivation of mature EC types in vivo provides the groundwork for a straightforward and robust in vitro differentiation protocol.

Previously, key roles for Notch and Retinoic Acid (RA) signaling pathways in the specification of murine arterial and hemogenic ECs, respectively, during development were identified. The Notch signaling pathway plays multiple roles in the specification and maintenance of the arterial EC phenotype. Work using the murine retinal vascularization model identified a pathway in which fluid shear stress induces a Notch-Cx37-p27 signaling axis, promoting G1 cell cycle arrest, which enables arterial EC specification²⁷. Cell cycle states have been hypothesized to play a role in cell fate decisions by providing distinct windows of opportunity in which cells are receptive to certain signals that can induce gene expression and phenotypic changes²⁸. This Notch-mediated G1 arrest enabled the expression of genes enriched in arterial ECs, including ephrinB2, Cx40, DLL4, Notch1, and Notch 4 (reviewed in^29,30). It has also been shown that hemogenic EC specification is promoted in vivo via RA signaling^31,32. Additional studies identified that, downstream of RA signaling, expression of c-Kit and Notch upregulate p27, which enables hemogenic specification in the murine yolk sac and AGM³³. Murine hemogenic ECs can be minimally identified by expression of both endothelial (i.e., CD31, KDR) and hematopoietic (i.e., c-Kit, CD34) markers⁴. Finally, hemogenic ECs undergo an endothelial-to-hematopoietic transition (EHT) to form HSPCs, which can give rise to all blood cell types^4,34,35.

Recent work tested whether this same signaling hierarchy can promote human hemogenic EC specification. To do so, a serum- and feeder-free 2D culture protocol to derive hemogenic ECs from hESCs was developed, and these hemogenic ECs were characterized on a single cell level as CD31⁺ KDR⁺ c-Kit⁺ CD34⁺ VE-Cadherin^- CD45^-. This study also took advantage of the Fluorescent Ubiquitination Cell Cycle Indicator (FUCCI) reporter, which identifies different cell cycle states, using H9-hESCs that express the FUCCI reporter construct (H9-FUCCI-hESC)³⁶. In studies with these cells, it was demonstrated that RA promotes early G1 cell cycle arrest in ECs, and early G1 state enables hemogenic specification in vitro³⁷. Herein, a detailed protocol for the differentiation of these human hemogenic endothelial cells and assays confirming their identity are provided. This straightforward method provides a useful means of generating this specialized subset of ECs for future studies of mechanisms of human blood cell development.

方案

1. Reagents and reagent preparation

NOTE: A list of reagents is provided in Table of Materials.

1. Obtain the human pluripotent stem cell lines: H1-hESC, H9-Fucci-hESC.
   NOTE: The generation of hemogenic ECs may be more efficient in the H1 cell line.
2. Prepare matrix protein stocks: Aliquot the matrix protein into pre-chilled 1.5 mL tubes (on ice) so that each tube contains 1 mg of matrix protein. 1 mg of matrix protein is enough to coat all wells of two 6-well plates (12 wells total). Store the aliquots at -20 °C until use.
   NOTE: Perform all the steps involving matrix protein on ice or at 4 °C. Thaw the frozen stock vial of matrix protein on ice at 4 °C overnight. Once thawed, swirl the vial to ensure the contents are mixed. Prechill 1.5 mL microcentrifuge tubes for at least 1 h at -20 °C and transfer to ice immediately prior to aliquoting.
3. Prepare matrix protein-coated plates: Thaw matrix protein aliquots on ice at 4 °C. Add 12.5 mL of ice-cold DMEM:F12 to a prechilled conical tube on ice. Utilizing pre-chilled pipette tips, transfer one aliquot (1 mg) of matrix protein to the conical tube and mix well by pipetting up and down. Aliquot 1 mL of the diluted matrix protein to each well of pre-chilled 6-well plates (on ice) using a pre-chilled serologic pipette. Swirl and rock the plates so that the entire well is coated evenly. Incubate the plates for a minimum of 30 min at room temperature to allow the matrix protein to solidify. Wrap the plates with parafilm and store at 4 °C until use. Use matrix protein-coated plates within 2 weeks of preparation.
   NOTE: Use the matrix protein-coated 6-well plates for routine passaging of cells and differentiation to primordial and hemogenic endothelial cells. Perform all the steps on ice. Pre-chill 6-well plates, pipette tips, serologic pipettes, and conical tubes prior to use for at least 1 h at -20 °C. Transfer these items to ice when ready to use.
4. Prepare the base differentiation medium by adding 5 mL of PFHM to 100 mL of pluripotent stem cell differentiation medium. Store at 4 °C.
5. Prepare 0.1% BSA-PBS by dissolving 0.1 g BSA in 100 mL PBS. Filter sterilize BSA-PBS by passing through a 0.22 μm filter and store at 4 °C.
6. Prepare 5 mM HCl by diluting stock HCl (12 M) 1:2,400 with water. Adjust the pH to 3.0 utilizing NaOH. Filter sterilize the solution by passing through a 0.22 μm filter and store at 4 °C.
7. Prepare bFGF, BMP4, VEGF-A, Retinoic Acid (RA), and DLL4 stocks.
   1. bFGF: Reconstitute the lyophilized powder to 100 μg/mL in 0.1% BSA-PBS. Aliquot and store at -20 °C. Use bFGF stocks within 3 months of preparation. Thaw the aliquots immediately prior to use.
   2. BMP4: Reconstitute the lyophilized powder to 1 mg/mL in 5mM HCl, pH 3.0. Further dilute to 50 μg/mL in 0.1% BSA-PBS. Aliquot and store at -20 °C. Use the BMP4 stocks within 3 months of preparation. Thaw the aliquots immediately prior to use.
   3. VEGF-A: Reconstitute the lyophilized powder to 1 mg/mL in dH₂O. Further dilute to 100 μg/mL in 0.1% BSA-PBS. Aliquot and store at -20 °C. Use the VEGF-A stocks within 3 months of preparation. Thaw the aliquots immediately prior to use.
   4. RA: Reconstitute the lyophilized powder to 100 mM in DMSO. Aliquot and store at -80 °C. Use the RA stocks within 1 month of preparation. Thaw the aliquots immediately prior to use.
      NOTE: Protect RA stocks from light.
   5. DLL4: Reconstitute the lyophilized powder to 1 mg/mL in PBS. Aliquot and store at -20 °C. Use the DLL4 stocks within 12 months of preparation. Thaw the aliquots immediately prior to use.
8. Prepare the endothelial cell differentiation medium immediately prior to use by diluting VEGF-A and BMP4 in base differentiation medium (step 1.4) so that the final concentrations are 25 ng/mL and 50 ng/mL, respectively.
9. Prepare the working RA immediately prior to use by diluting 100 mM stock 1:1,000 in DMSO to 100 μM.
   NOTE: Protect working RA from light.
10. Prepare the hemogenic endothelial cell differentiation medium immediately prior to use by diluting VEGF-A, BMP4, and working RA in base differentiation medium (step 1.4) so that the final concentrations are 25 ng/mL, 50 ng/mL, and 0.5 μM, respectively.
11. Prepare the antibody staining buffer by making HBSS containing 10% FBS and supplement with 1:500 diluted antimicrobial reagent. Sterile filter the buffer and use immediately.
12. Prepare the cell sorting buffer by making HBSS containing 1% FBS and supplement with 1:500 diluted antimicrobial reagent. Sterile filter the buffer and use immediately.
13. Prepare 1 mg/mL fibronectin stocks by adding 5 mL of sterile water to 5 mg lyophilized fibronectin. Aliquot and store at -20 °C. Use the fibronectin stocks prior to the expiry date on the lyophilized product label. Thaw the aliquots immediately prior to use.
14. Prepare the fibronectin-coated 35 mm dishes. Dilute the fibronectin stocks (1 mg/mL) to 4 μg/mL in sterile water. Add 1 mL of this fibronectin coating solution to each dish and incubate at 37 °C for 30 min to 1 h. Use the dishes immediately following coating.
15. Prepare 3 or 4 mL aliquots of methylcellulose-based medium following the manufacturer's instructions. Store the aliquots at -20 °C until use. Use the methylcellulose-based medium aliquots prior to the expiry date indicated on the stock product label. Thaw the aliquots immediately prior to use.
16. Prepare the DLL4 coating solution by diluting recombinant human DLL4 stock to a final concentration of 10 μg/mL in PBS.
17. Prepare and store the endothelial cell growth medium according to the manufacturer's instructions.
18. Prepare the flow cytometry analysis buffer by making PBS containing 0.1% BSA. Sterile filter the buffer and store at 4 °C until use.

2. Cell culture and passaging of hESCs

1. Allow the matrix protein-coated plates, stem cell growth medium, and DMEM:F12 to warm to room temperature.
2. Grow the hESC cell lines in stem cell growth medium (2 mL/well) on matrix protein-coated 6-well plates in a 37 °C, 5% CO₂ incubator.
3. Check the cells daily and remove the differentiated cells as necessary by gently scraping them off the plate using a p200 pipette tip.
   NOTE: Differentiated cells will appear on the periphery of colonies. Refer to the stem cell growth medium product manual for examples of differentiated cells in culture.
4. Passage the cells once they reach 70%-80% confluency. To passage cells, perform the following steps.
   NOTE: Cells should be split prior to reaching 70%-80% confluency if increased differentiation occurs.
   1. Remove the medium above the cells and gently wash with 1 mL DMEM:F12 per well.
   2. Add 1 mL of DMEM:F12 per well.
   3. Add 160 μL/mL of Dispase per well and incubate the cells at 37 °C in a 5% CO₂ incubator for 45 min.
   4. Following Dispase incubation, add an additional 1 mL of DMEM:F12 per well and gently pipette to lift the cells.
      NOTE: Avoid dissociating the cells into a single-cell suspension. Passage the cells as small clumps.
   5. Transfer the cells to a conical tube containing 12 mL of DMEM:F12 and allow the cells to settle by gravity (~5-10 min).
   6. Remove the supernatant and gently resuspend the pellet in 0.5 mL of stem cell growth medium per well of lifted cells to obtain small clumps of cells.
      NOTE: Avoid dissociating the cells into a single-cell suspension. Passage the cells as small clumps.
   7. Aspirate the matrix protein coating solution from the wells of the prepared matrix protein-coated plate and add 1.5 mL of the stem cell growth medium per well.
   8. Add the desired volume of resuspended cells (step 2.4.6) to each well of the prepared matrix protein-coated plate.
   9. Incubate the plate in a 37 °C, 5% CO₂ incubator. Change the medium every 24 h to fresh stem cell growth medium.

3. Differentiation of hESCs to primordial endothelial cells

1. Day -1: Culture and passage the cells as described above in section 2. Seed the cells (step 2.4.6) in small clumps (~50 μm) at a density of approximately 2 clumps per square centimeter³⁸.
   NOTE: Evaluate the seed density and refine empirically if necessary.
2. Day 0: 24 h after seeding the cells, aspirate the medium from each well and gently wash the cells with 1 mL DMEM:F12 per well. Add 1 mL of the base differentiation medium containing 5 μM GSK3i (CHIR99021, added fresh) to each well and incubate for 24 h (37 °C, 5% CO₂).
   NOTE: For all the wash steps, slowly add the indicated wash media to the plate by pipetting against the wall of the plate well. Gently swirl the plate so that the entire surface of the well is covered by wash media. Slightly tilt the plate so that the wash media pools at the six o-clock position and carefully aspirate the wash media.
3. Day 1: Aspirate the medium from each well and gently wash the cells with 1 mL DMEM:F12 per well. Add 1 mL of the base differentiation medium containing 50 ng/mL bFGF (added fresh, 1:2,000 from frozen stock) to each well and incubate 24 h (37 °C, 5% CO₂).
4. Day 2: Aspirate the medium from each well and gently wash the cells with 1 mL of DMEM:F12 per well. Add 1 mL of the endothelial cell differentiation medium to each well and incubate 24 h (37 °C, 5% CO₂).
5. Day 3: Replace the medium above the cells with 1 mL of freshly prepared endothelial cell differentiation medium per well and incubate 24 h (37 °C, 5% CO₂).
6. Day 4: Replace the medium above the cells with 1 mL of freshly prepared endothelial cell differentiation medium per well and incubate 24 h (37 °C, 5% CO₂).
7. Day 5: FACS purify the cells to assess EC phenotype (sections 4-5) or keep in culture and differentiate towards hemogenic endothelial cells (section 6).

4. FACS purification of primordial endothelial cells

1. Aspirate the medium above the cells and gently wash once with 1 mL of DMEM:F12 per well.
2. Add 1 mL of cell detachment solution per well and incubate the cells for 12 min in a 37 °C, 5% CO₂ incubator, or until cells have dissociated.
3. Transfer the dissociated cells to a conical tube containing 12 mL of DMEM:F12 and pellet by centrifugation for 5 min, 1,000 x g.
4. Remove the supernatant and resuspend the pellet in 12 mL of DMEM:F12 to wash.
5. Pellet the cells by centrifugation for 5 min, 1,000 x g.
6. Remove the supernatant and resuspend the cell pellet in ice-cold antibody staining buffer and count the cells. Adjust the concentration using ice-cold antibody staining buffer to 1 x 10⁵ cells/mL.
7. Divide the cells evenly into microcentrifuge tubes on ice, each containing a minimum of 600 μL cells at 1 x 10⁵ cells/mL, for antibody staining.
   NOTE: Four tubes of cells are required for staining of primordial ECs: unstained control, CD31 single antibody control, CD45 single antibody control, and sample containing both CD31 and CD45 antibodies. Information about antibodies is provided in Table of Materials.
8. Add antibodies to the tubes containing cells, as appropriate, and incubate on ice and protected from light for 30 min.
   1. Unstained control: Do not add any antibody.
   2. CD31 single antibody control: Add only CD31 antibody.
   3. CD45 single antibody control: Add only CD45 antibody.
   4. Sample: Add both CD31 and CD45 antibodies.
      NOTE: The final antibody concentration in the sample, as well as the fluorescent conjugates, should be optimized based on the specific antibodies and cell sorter used.
9. Pellet the cells by centrifugation in a 4 °C tabletop microcentrifuge for 5 min at 1,000 x g.
10. Remove the supernatant and resuspend the cell pellets in 600 μL of ice-cold sorting buffer.
11. Strain the samples through the mesh filter caps of 5 mL FACS tubes and store the cells on ice, protected from light, for immediate FACS.
12. Obtain primordial endothelial cells (CD31⁺ CD45^-), by performing the following steps.
    1. Identify the CD45-negative cell population and gate (CD45^-).
    2. Within (CD45^-), identify the CD31-positive (CD31⁺) cell population and sort cells into 6 mL ice-cold cell sorting buffer. Use these cells for downstream applications (see section 5).

5. Assay to confirm primordial endothelial cell phenotype

1. Coat three wells of a 6-well plate with 1 mL/well DLL4 coating solution for 30 min in a 37 °C, 5% CO₂ incubator. As a control, mock-coat the other three wells of the plate with 1 mL/well PBS.
2. Aspirate the DLL4 coating solution and PBS, and plate 25,000 sorted primordial endothelial cells (see step 4.12) in 2 mL of endothelial cell growth medium per well.
3. Incubate the cells for 24 h in a 37 °C, 5% CO₂ incubator.
4. Aspirate the medium above the cells and wash once with 2 mL/well PBS. Analyze the cells by qPCR or flow cytometry (for cells expressing the FUCCI construct).
   1. To analyze the cells by qPCR, perform the following steps.
      1. Aspirate the liquid above the cells and isolate the RNA in the cells using an RNA extraction kit according to the manufacturer's protocol.
      2. Perform reverse transcription reactions with a reverse transcription master mix according to the manufacturer's protocol.
      3. Perform qPCR reactions with a SYBR Green master mix according to the manufacturer's protocol.
         NOTE: Primers utilized (EFNB2, GJA5, GJA4, NR2F2, EPHB4, HEY2) are listed in Table 1.
   2. To analyze cells expressing the FUCCI construct by flow cytometry, perform the following steps.
      1. Aspirate the liquid above the cells and add 500 μL/well 0.25% trypsin-EDTA.
      2. Incubate the cells at 37 °C in a 5% CO₂ incubator until lifted, ~5 min.
      3. Transfer the cells to a microcentrifuge tube and pellet the cells in a 4 °C microcentrifuge for 5 min at 1,000 x g.
      4. Aspirate the supernatant and resuspend the pellet in 500 μL of ice-cold flow cytometry analysis buffer.
      5. Strain the samples through the mesh filter cap of a 5 mL FACS tube and store the cells on ice, protected from light, for immediate flow cytometry analysis.
      6. Analyze the percentage of cells plated on DLL4 vs. PBS control in early G1 (no color), late G1 (mCherry⁺/mVenus^-), G1/S (mCherry⁺/mVenus⁺), and S/G2/M (mCherry^-/mVenus⁺).

6. Differentiation of hESCs to hemogenic endothelial cells

NOTE: Differentiate the cells to day 4 primordial ECs, as described above in sections 3.1-3.6.

1. Day 5: Aspirate the medium above the cells and gently wash the cells with 1 mL of DMEM:F12 per well. Add 1 mL of freshly prepared hemogenic endothelial cell differentiation medium per well and incubate 24 h (37 °C, 5% CO₂).
2. Day 6: Replace the medium above the cells with 1 mL of freshly prepared hemogenic endothelial cell differentiation medium per well and incubate 24 h (37 °C, 5% CO₂).
3. Day 7: Replace the medium above the cells with 1 mL of freshly prepared hemogenic endothelial cell differentiation medium per well and incubate 24 h (37 °C, 5% CO₂).
4. Day 8: FACS isolate hemogenic endothelial cells (see section 7).

7. FACS-isolation of hemogenic endothelial cells

1. Lift and wash the cells as described above in sections 4.1-4.6.
2. Divide the cells evenly into microcentrifuge tubes on ice, each containing a minimum of 600 μL cells at 1 x 10⁵ cells/mL, for antibody staining.
   ​NOTE: Eight tubes of cells are required for antibody staining of hemogenic ECs: unstained control, CD31 single antibody control, CD45 single antibody control, KDR single antibody control, c-Kit single antibody control, CD34 single antibody control, VE-cadherin single antibody control, and sample containing all six antibodies.
   NOTE: Antibody information is provided in Table of Materials.
3. Add antibodies to the tubes containing cells, as appropriate, and incubate on ice and protected from light for 30 min.
   1. Unstained control: Do not add antibody.
   2. CD31 single antibody control: Add only CD31 antibody.
   3. CD45 single antibody control: Add only CD45 antibody.
   4. KDR single antibody control: Add only KDR antibody.
   5. c-Kit single antibody control: Add only c-Kit antibody.
   6. CD34 single antibody control: Add only CD34 antibody.
   7. VE-cadherin single antibody control: Add only VE-cadherin antibody.
   8. Sample: Add CD31, CD45, KDR, c-Kit, CD34, and VE-cadherin antibodies.
      NOTE: The final antibody concentration in the sample, as well as the fluorescent conjugates, should be optimized based on the specific antibodies and cell sorter used.
4. Pellet the cells by centrifugation in a 4 °C microcentrifuge for 5 min at 1,000 x g.
5. Remove the supernatant and resuspend the pellets in 600 μL of ice-cold sorting buffer.
6. Strain the samples through the mesh filter cap of 5 mL FACS tubes and store cells on ice, protected from light, for immediate FACS.
7. To obtain hemogenic endothelial cells (CD31⁺ KDR⁺ c-Kit⁺ CD34⁺ VE-Cadherin^- CD45^-), perform the following steps.
   1. Identify the CD45^- cell population and gate (CD45^-).
   2. Within (CD45^-), identify the CD31⁺ cell population and gate (CD31⁺).
   3. Within (CD31⁺), identify the VE-Cadherin^- cell population and gate (CDH5^-).
   4. Within (CDH5^-), identify the c-Kit⁺ cell population and gate (KIT⁺).
   5. Within (KIT⁺), identify the CD34⁺ cell population and gate (CD34⁺).
   6. Within (CD34⁺), identify and sort the KDR⁺ cells into 6 mL ice-cold cell sorting buffer. Use these cells in downstream applications (see section 8).

8. Colony forming unit assay

1. Thaw the aliquots of methylcellulose-based medium following the manufacturer's instructions.
   NOTE: One 3 mL aliquot is sufficient for two samples and one 4 mL aliquot is sufficient for three samples.
2. Count the sorted hemogenic endothelial cells obtained in step 7.7.
3. Following the manufacturer's instructions, calculate the volume of sorted cells to add to each methylcellulose-based medium aliquot so that each sample will contain a minimum of 1,000 hemogenic endothelial cells.
   NOTE: The number of cells can be adjusted as necessary.
4. Add the calculated volume of cells to the methylcellulose-based medium aliquot and vortex thoroughly. Allow the methylcellulose-based medium cultures to sit at room temperature for 10 min, or until the bubbles dissipate.
5. Aspirate the fibronectin coating solution from the prepared 35 mm dishes. Following the manufacturer's instructions, dispense 1 mL of methylcellulose-based medium culture per 35 mm dish. Gently rotate the dish to evenly distribute the culture.
6. Place these 35 mm dishes, as well as two additional 35 mm dishes filled with sterile water, within a 15 cm tissue culture dish.
7. Incubate the cultures in a 37 °C, 5% CO₂ incubator, and observe the cultures on days 8 and 14.
   1. On day 8, count the CFU-E and BFU-E colonies.
   2. On day 14, count the CFU-GM and CFU-GEMM colonies.
      NOTE: Refer to the methylcellulose-based medium manual for morphological identification of colony types.

结果

A schematic outlining the specification of primordial ECs and hemogenic ECs from hESCs, and a representative image of cells 24 h after plating are shown in Figure 1. Following specification, primordial ECs and hemogenic ECs are FACS purified on days 5 and 8, respectively. Primordial ECs are defined as CD31⁺ CD45^- and hemogenic ECs are defined as CD31⁺ KDR⁺ c-Kit⁺ CD34⁺ VE-Cadherin^- CD45^-. A representative...

讨论

Herein, the steps for producing hemogenic endothelial cells from human embryonic stem cells in approximately 1 week using a murine feeder- and serum-free 2D culture system (Figure 1) are outlined. This protocol expands on a method described by Sriram et al. (2015) to obtain primordial ECs³⁸. The primordial nature and specification potential of the CD31⁺ CD45^- ECs is demonstrated by culturing these cells on DLL4-coated plates and observing gene ex...

材料

本文使用的材料清单

姓名	公司	目录编号	评论
15 cm 培养皿	康宁	430599	组织培养处理
35 mm 培养皿	康宁	430165	组织培养处理
6 孔板	康宁	3516	组织培养处理
抗菌试剂 品牌名称：Normocin	Invitrogen	ant-nr-1
bFGF	R&D 系统	233-FB-025	以 50 ng/mL
BMP4		595202	在 25 ng/mL 牛
血清白蛋白 （BSA）	Scientific	BP1600-1
细胞分离溶液 品牌名称：Accutase	Stemcell Technologies	7920
二甲基亚砜 （DMSO）	Sigma Aldrich	D2650-100mL
Dispase	Stemcell Technologies	7913
DLL4	研发D 系统	1506-D4/CF	重组人;在 10 &μ 处使用;g/mL
DMEM：F12	Gibco	11320-033
Dulbecco 磷酸盐缓冲盐水 （PBS）	Gibco	14190144
内皮细胞生长培养基 品牌名称：EGM-2 内皮细胞生长培养基-2 BulletKit （EGM-2）	Lonza	CC-3162
FACS 管	康宁	352235	聚苯乙烯圆底带过滤帽
胎牛血清 （FBS）	Gemini Bio	100-106
纤连蛋白	ThermoFisher Scientific	33016015	在 4 &mu 使用;g/cm2
GSK3i/CHIR99021	Stemgent	04-0004-02	10 mM 原液;5 μ 用;M
Hanks 平衡盐溶液 （HBSS）	Gibco	14175-095
盐酸 （HCl）	Fisher Scientific	A144S-500
基质蛋白  品牌名称：Matrigel	Corning	356230	生长因子降低。请参阅批次的分析证书，以确定蛋白质 （Matrigel） 浓度。计算含有 1 mg 蛋白质的 Matrigel 的体积需要该浓度。
甲基纤维素基培养基 品牌名称：MethoCult H4435 富集	技术	4435
多能干细胞分化培养基 品牌名称：STEMdiff APEL 2	Stemcell Technologies	5270
多能干细胞：H1、H9、H9-FUCCI	WiCell	WA09 （H9）、WA01 （H1）	人;H9-FUCCI 购自剑桥干细胞研究所 Ludovic Vallier 博士的实验室
无蛋白杂交瘤培养基 （PFMH）	Gibco	12040077
视黄酸	Sigma Aldrich	R2625-50mg	使用 0.5 μ;M
逆转录预混液 品牌名称：iScript 逆转录超混合液	BioRad	1708840
RNA 提取试剂盒 品牌名称：RNeasy 迷你试剂盒	Qiagen	74104
氢氧化钠 （NaOH）	Fisher Scientific	SS255-1
干细胞生长培养基 品牌名称：mTeSR1	Stemcell Technologies	85850
SYBR Green 预混液 品牌名称：iTaq Universal SYBR Green 预混液	BioRad	1725121
胰蛋白酶-EDTA	Gibco	25299956	0.25%
VEGF< sub>165 （VEGF-A）	PeproTech	100-20	以 50 ng/mL
α-CD31-FITC	BioLegend	303104	2 &μ;g/mL*
α-CD34-Pacific Blue	BioLegend	343512	2 &μ;g/mL*
α-CD45-APC/Cy7	BioLegend	304014	2 &μ;g/mL*
α-c-试剂盒-APC	BioLegend	313206	2 μg/mL*
α-Flk-1-PE/Cy7	BioLegend	359911	2 &μ;g/mL*
α-VE-钙粘蛋白-PE	BioLegend	348506	2 &μ;g/mL*
* 抗体荧光偶联物应根据所使用的细胞分选仪进行优化。这里介绍的是本研究中使用的最终浓度。