Method Article

Reconstruct Human Retinoblastoma In Vitro

DOI:

10.3791/62629

October 11th, 2022

In This Article

Summary

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We describe a method for generating human retinoblastoma (RB) by introducing biallelic RB1 mutations in human embryonic stem cells (hESC). RB cell lines could also be successfully cultured using the isolated RB in a dish.

Abstract

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Human RB is pediatric cancer, which is lethal if no treatment is administered. As RB originates from cone precursors, which is relatively rare in rodent models, meanwhile regarding the interspecies differences between humans and rodents, a disease model derived from humans is more beneficial for uncovering the mechanisms of human RB and seeking the targets of therapy. Herein, the protocol describes the generation of two gene-edited hESC lines with a biallelic RB1 point mutation (RB1Mut/Mut) and an RB1 knockout mutation (RB1-/-), respectively. During the process of retinal development, the formation of RB is observed. The RB cell lines are also established by segregating from the RB organoids. Altogether, by differentiating the gene-edited hESC lines into the retinal organoids using a 2D and 3D combined differentiation protocol, we have successfully reconstructed the human RB in a dish and identified its cone-precursor origin. It would provide a helpful disease model for observing the retinoblastoma genesis, proliferation, and growth as well as further developing novel therapeutic agents.

Introduction

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Human retinoblastoma (RB) is a rare, fatal tumor derived from the retinal cone-precursors1,2,3, is the most common type of intraocular malignancy in childhood4. Homozygous inactivation of RB1 gene is the initiating genetic lesion in RB5. However, mice with RB1 mutations fail to form the retinal tumor2. Although the mouse tumors could be generated with the combination of Rb1 mutations and other genetic modifications, they still lack the features of human RB6

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Protocol

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This study is approved by the institutional Ethics Committee of Beijing Tongren Hospital, Capital Medical University. H9 hESCs are obtained from the WiCell Research Institute.

1. Generation of RB1 mutated hESC

  1. CRISPR/Cas9 targeting vector for the knockout (KO) of RB1.
    1. Design a pair of sgRNA. For the ablation of RB1, target the first exon of this gene. The forward primer sequence is CACCGCGGTGGCGGCCGTTTTTCGG, and the reverse primer sequence is AAACCCGAAAAACGGCCGCCACCGC.
      NOTE: For the specific RB1 mutation, a repaired template is also required. In this protocol, RB1....

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Results

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The procedure of RB generation is elucidated in the Figure 1, which combines the adherent and floating culture. It was possible to harvest the human RB from RB1-KO hESC, and obtain the RB cell line by isolating the RB organoids.

Here, the protocol provides the details of the differentiation in different stages (Figure 2). Hollow spheres are formed in the first 3 days which attach to the culture surface and then expand (

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Discussion

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Human retinoblastoma (RB) is caused by the inactivation of RB1 and the dysfunction of Rb protein. In this protocol, the RB1-KO hESC is the pivotal step for the generation of RB in a dish. While even with RB1-/- hESC, it is possible that there is no RB formation due to the methods of retinal organoid differentiation10. In this protocol, the transfer from adherent culture to floating culture is essential in the process of differentiation. The density of the cyst.......

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Disclosures

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The authors are not aware of any affiliations, memberships, funding, or financial holdings that might affect the objectivity of this study.

Acknowledgements

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We thank the 502 team for all the help. This work is partly supported by the Beijing Municipal Natural Science Foundation (Z200014) and National Key R&D Program of China (2017YFA0105300).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
2-mercaptoethanolLife Technologies21985-023
Anti-ARR3SigmaHPA063129Antibody
Anti-CRX (M02)AbnoveABN-H00001406-M02Antibody
Anti-Ki67Abcam ab15580Antibody
Anti-Syk (D3Z1E)Cell Signaling Technology13198Antibody
BbsINEBR3539SRestriction enzymes
Dispase (1U/mL)Stemcell Technologies7923
DMEM basicGibco10566-016
DMEM/F-12-GlutaMAXGibco10565-042
DMSOSigmaD2650
DPBSGibcoC141905005BT
EDTAThermo15575020
Fetal Bovine Serum (FBS), Qualified for Human Embryonic Stem CellsBiological Industry04-002-1A
GlutamineGibco35050-061
Ham's F-12 Nutrient Mix (Hams F12)Gibco11765-054
MEM Non-essential Amino Acid Solution (100X)SigmaM7145
Neurobasal MediumGibco21103-049
P3 Primary Cell 4D-Nucleofector X Kit SLonzaV4XP-3032Nucleofection kit
Pen StrepGibco15140-122
PuromycinGene OperationISY1130- 0025MG
QIAquick PCR Purification KitQIAGEN28104
ncEpic-hiPSC/hESC culture mediumNuwacellRP01001ncEpic-hiPSC/hESC culture medium in 1.2.1
Growth factor reduced basement membrane matrixBD356231Matrigel in 1.2.1
Cell dissociation enzymeGibco12563-011TrypLE Express in 1.2.8
RNeasy Midi KitQIAGEN75144
RNeasy Mini KitQIAGEN74104
Supplement ALife Technologies17502-048N-2 Supplement (100X), liquid, supplemet in medum I
Supplement BLife Technologies17105-041B-27 Supplement (50X),liquid, supplemet in medum I,II,III
T4 Polynucleotide KinaseLife TechnologiesEK0032
TaurineSigmaT-8691-25G
Y-27632 2HClSelleckS1049
pX330-U6- Chimeric BB-CBh-hSpCas9-2A-PuroAddgene42230
Nucleofector 4DLonza
RPMISigmaR0883-500ML

References

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  1. Liu, H., et al. Human embryonic stem cell-derived organoid retinoblastoma reveals a cancerous origin. Proceedings of the National Academy of Sciences of the United States of America. 117 (52), 33628-33638 (2020).
  2. Singh, H. P., et al.

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Tags

Retinal OrganoidsRB1 KnockoutCone Precursor CellsIn Vitro Cancer ModelHuman Embryonic Stem CellsRetinoblastoma Genesis3D Cell DifferentiationProliferation Marker Ki67Optic Vesicle Architecture

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