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Paralog 4 HOX Genes HOXA4 and HOXB4 Expand Pro-B Cells in Vitro

2011· article· en· W2587085973 on OpenAlexaff
Marilaine Fournier, Charles‐Étienne Lebert‐Ghali, Mona Hassawi, Janet J. Bijl

Bibliographic record

VenueBlood · 2011
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBiological Activity of Diterpenoids and Biflavonoids
Canadian institutionsUniversité de MontréalHôpital Maisonneuve-Rosemont
Fundersnot available
KeywordsBiologyProgenitor cellHaematopoiesisStem cellMyeloidBone marrowHox geneMolecular biologyCell cultureCell biologyCancer researchImmunologyGeneGene expressionGenetics

Abstract

fetched live from OpenAlex

Abstract Abstract 1299 HOX genes are known for their involvement in self-renewal of normal and malignant hematopoietic stem cells (HSC). Enforced expression of HOXB4 leads to HSC expansion in vitro and in vivo without leukemia development. We have recently shown that overexpression of its paralog HOXA4 also resulted in an increase of HSCs and myeloid progenitors in vitro. HOXA4 HSC are fully functional and reconstitute mouse chimeras with normal ratios of mature cells in the periphery. Interestingly, although the mature B-cell compartment is not enhanced, the overexpression of HOXA4 resulted in a 10-fold expansion of B-cell progenitors in the bone marrow (BM). Moreover, the number of more primitive WW-IC was not affected by the overexpression of HOXA4, indicating that this gene specifically expands IL-7 responsive B-cell progenitors. Based on these observations in vivo, we sought to determine if paralog 4 HOX genes can expand B-cell progenitors in vitro. To test this B220+ cells were sorted from BM of healthy wild type mice and transduced with MSCV retroviral vectors for HOXA4-GFP, HOXB4-GFP or control-GFP. Cells were cultured in B-cell specific medium and their growth in response to IL-7 was followed for three weeks. We observed a 15- and 10-fold increase of growth for HOXA4 and HOXB4 pro-B cells compared to control, respectively, within 16 days. FACS analysis confirmed the pro-B cell phenotype of all three cultures. These cells are currently being tested for their repopulation capacity of the B-cell compartment in irradiated hosts. To further investigate potential implication of these genes in oncogenic transformation HOXA4 and HOXB4 were overexpressed in E2APBX1 B-cells derived from E2APBX1 transgenic mice. We showed that the overexpression of HOXA4 or HOXB4 induced a strong expansion of E2APBX1 pro-B cell in vitro (2381- and 1090-fold difference over the control after 23 days, respectively), leading to an immortalization of the culture. Despite this huge expansion these cells were incapable to initiate leukemia upon transfer into irradiated recipients. B-CFC assays showed that the growth of HOXA4 or HOXB4 E2APBX1 pro-B cell cultures was supported by a strong expansion of B-cell progenitors (6138- and 15307-fold difference over the control after 20 days, respectively). Taken together, these results indicate that IL-7 responsive pro-B-cell progenitors are sensitive to paralog 4 HOX genes, an effect which is dramatically enhanced in the context of E2APBX1. Lack of clear oncogenic potential puts HOXA4 and –B4 forward as promising candidates to expand B-cell progenitors in vitro. These cells could potentially be used for B-cell complementation therapy in BM transplantation recipients. Disclosures: No relevant conflicts of interest to declare.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.011
Threshold uncertainty score0.470

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.019
GPT teacher head0.214
Teacher spread0.195 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2011
Admission routes1
Has abstractyes

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