STEMdiff™ T细胞试剂盒

用于hPSC向T细胞的扩增和分化

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产品号 #（选择产品）

产品号 #100-0194_C

用于hPSC向T细胞的扩增和分化

产品优势

配方中不含血清，无须使用饲养层。
均一化拟胚体生成
兼容多株ES和iPS细胞系稳定生成CD4+CD8+ 双阳T细胞

产品组分包括

STEMdiff™造血分化 - EB基础培养基，120 mL（产品号# 100-0171）
STEMdiff™造血分化 - EB补充剂 A，265 μL（产品号# 100-0172）
STEMdiff™造血分化 - EB补充剂 B，7 mL（产品号#100-0173）
StemSpan™ SFEM II（产品号 #09605）
StemSpan™淋系祖细胞扩增补充剂(10X)，5 mL（产品号# 09915）
StemSpan™淋系分化包被材料(100X)，2 x 0.25 mL（产品号# 09925）
StemSpan™ T细胞祖细胞成熟添加物（10X）（产品号# 09930）

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总览

使用无饲养层、无血清的STEMdiff™ T 细胞分化试剂盒将人多能干细胞(hPSCs)分化为T细胞

STEMdiff™ T细胞分化试剂盒方案首先采用无动物成分的STEMdiff™造血分化 - EB试剂，从hPSCs生成拟胚体(EBs)，随后进一步分化为CD34+细胞。本试剂盒包含该步骤所需全部EB试剂：
• STEMdiff™造血分化 - EB基础培养基
• STEMdiff™造血分化 - EB补充剂 A
• STEMdiff™造血分化 - EB补充剂 B

随后使用StemSpan™试剂将CD34+细胞进一步定向分化为T细胞：
• StemSpan™ SFEM II
• StemSpan™淋系祖细胞扩增补充剂(10X)
• StemSpan™淋系分化包被材料(100X)
• StemSpan™ T细胞祖细胞成熟添加物(10X)

为方便使用，试剂盒内所有STEMdiff™造血分化 - EB及StemSpan™试剂均可单独购买

Data Figures

Figure 1. STEMdiff™ Hematopoietic - EB Progenitor Differentiation Protocol

hPSCs are harvested and dissociated into a single-cell suspension prior to seeding into AggreWell™ plates in EB Formation Medium (EB Medium A + 10 μM Y-27632) to form 600-cell aggregates. After 3 days of mesoderm formation, the medium is changed to EB Medium B to induce hematopoietic lineage differentiation. On day 5, EBs are transferred onto non-tissue culture-treated plates. After a total of 12 days, EBs are harvested and dissociated, and CD34+ cells are then enriched by EasySep™ positive selection.

Figure 2. hPSCs Differentiate to CD34+ Hematopoietic Progenitor Cells After 12 Days of Culture

Human ES and iPS cells were induced to differentiate to CD34+ cells using the 12-day protocol shown in Figure 1. At the end of the culture period, cells were harvested, dissociated into a single-cell suspension, and analyzed by flow cytometry for CD34 and CD144 expression. Dead cells were excluded by light-scatter profile and DRAQ7™ staining. Representative flow cytometry plot for (A) ES (H1) cell-derived and (B) iPS (STiPS-F016) cell-derived cells analyzed on day 12 are shown. (C) The average frequency of viable CD34+ cells on day 12 (before CD34+ cell isolation) for two ES cell lines (H1 and H9) and three iPS cell lines (WLS-1C, STiPS-M001, and STiPS-F016) ranged between 31% and 51%. The average yield of CD34+ cells produced per well of a 6-well AggreWell™400 plate ranged between 4.0 x 10⁵ and 6.7 x 10⁵. Data are shown as mean ± SEM (n = 9 - 35). Results are representative of populations prior to magnetic cell separation.

Figure 3. T Cell Generation Protocol

hPSC-derived CD34+ cells are seeded in StemSpan™ Lymphoid Progenitor Expansion Medium on plates coated with StemSpan™ Lymphoid Differentiation Coating Material. On day 14, cells at the lymphoid progenitor stage are harvested and reseeded in StemSpan™ T Cell Progenitor Maturation Medium onto coated plates for further differentiation to CD4+CD8+ DP T cells. The DP T cells are harvested after 28 days.

Figure 4. hPSC-Derived CD34+ Cells Differentiate to CD5+CD7+ Lymphoid Progenitor Cells Over 14 Days of Culture

hPSC-derived CD34+ cells were cultured for 14 days in StemSpan™ SFEM II + StemSpan™ Lymphoid Progenitor Expansion Supplement on plates coated with StemSpan™ Lymphoid Differentiation Coating Material (Figure 3). Cells were harvested and analyzed for CD7 and CD5 expression by flow cytometry. Representative flow cytometry plots for (A) ES (H1) cell-derived and (B) iPS (STiPS-F016) cell-derived cells are shown. (C) The average frequency of viable CD7+CD5+ lymphoid progenitor cells on day 14 ranged between 38% and 54%, and the average yield of lymphoid progenitor cells produced per input hPSC-derived CD34+ cell was between 12 and 40. Data are shown as mean ± SEM (n = 8 - 32).

Figure 5. CD4+CD8+ DP T Cells Can Be Generated from Human hPSC-Derived CD34+ Cells After 28 Days of Culture

DP T cells were differentiated from hPSC-derived CD34+ cells as described (Figure 3). Cells were harvested and analyzed for expression of CD3, CD4, CD8, and TCRαβ by flow cytometry. Representative flow cytometry plots are shown for (A,B) ES (H1) cell-derived and (C,D) iPS (STiPS-F016) cell-derived cells. (E) The average frequency of viable CD4+CD8+ DP T cells on day 28 ranged between 23% and 58%, and the average yield of DP T cells produced per input hPSC-derived CD34+ cell was between 12 and 108. (F) The average frequency of CD3+TCRαβ+ expressed on DP T cells ranged between 11% and 38%. Data are shown as mean ± SEM (n = 6 - 17).

Figure 6. Optional CD8+ SP T Cell Maturation Protocol

DP T cells are seeded in CD8+ SP T Cell Maturation Medium supplemented with ImmunoCult™ T Cell Activator on plates coated with StemSpan™ Lymphoid Differentiation Coating Material. CD8+ SP T cells can be harvested after 7 days.

Figure 7. hPSC-Derived CD4+CD8+ DP T Cells Are Able to Mature to CD8+ SP T Cells

hPSC-derived CD34+ cells were first differentiated to DP T cells during 28 days of culture (Figure 3), and were then matured to CD8+ SP T cells using an additional 7-day maturation protocol (Figure 6). Cells were harvested and analyzed by flow cytometry for expression of (A,D) CD3 and TCRαβ, (B,E) CD4 and CD8 (gated on CD3+TCRαβ+), and (C,F) CD8α and CD8β (gated on CD8+ SP). Representative results for (A,B,C) ES (H1) cell-derived and (D,E,F) iPS (STiPS-F016) cell-derived cells are shown. (G) The average frequency of CD3+TCRαβ+CD4-CD8+ (CD8+SP) T cells was between 3% and 28%. Data are shown as mean ± SEM (n = 2 - 9).

Figure 8. hPSC-Derived CD8+ SP T Cells Can Be Induced to Express Activation Markers CD25 and CD69, Degranulate, and Produce IFN-γ

hPSC-derived CD34+ cells were first differentiated to DP T cells during 28 days of culture and then matured to CD8+ SP T cells using an additional 7-day maturation protocol (Figures 3 and 6). CD8+ SP T cells were sorted using fluorescence-activated cell sorting and cultured for 7 days in ImmunoCult™-XF T Cell Expansion Medium supplemented with IL-2 and stimulated with ImmunoCult™ Human CD3/CD28 T Cell Activator. Cells were harvested and analyzed by flow cytometry for expression of (A,D) CD25 and CD69. For assessment of degranulation and cytokine production, at 4 hours prior to harvest, some cells were also stimulated with phorbol 12-myristate 13-acetate (PMA) and ionomycin. After one hour, monensin and brefeldin A were added to each well to inhibit protein transport. Control (unstimulated; black histogram) and PMA + ionomycin-stimulated cells (orange histogram) were additionally analyzed by flow cytometry for surface expression of (C,F) CD107a (lysosomal-associated membrane protein 1 or LAMP-1) indicating degranulation and intracellular expression of (B,E) IFN-γ (gated on CD8+ SP). Representative results for (A,B,C) ES (H1) cell-derived and (D,E,F) iPS (STiPS-F016) cell-derived cells are shown.

Protocols and Documentation

Find supporting information and directions for use in the Product Information Sheet or explore additional protocols below.

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Product Information Sheet

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STEMdiff™ T Cell Kit

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