Evidence map›Paper›PMID 42734770›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2027

Enhancing the Functionality of Human Bone Marrow-Derived Mesenchymal Stromal Cells Using Signaling Modulators.

Vaijayanti Kale

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Article in Methods in molecular biology (Clifton, N.J.), 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Vaijayanti KaleSymbiosis Centre for Stem Cell Research, Symbiosis International University, Pune, India. vaijayanti.kale@ssbs.edu.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone marrow-derived mesenchymal stem/stromal cells (BM-MSCs) possess an inherent capacity to support hematopoiesis in vitro. As a result, they are often used as feeder layers for the ex vivo expansion of hematopoietic stem cells (HSCs) or coinfused with HSCs to improve the success of clinical transplants. However, MSCs isolated from non-hematopoietic tissues such as adipose or dental tissue may not be as effective as BM-MSCs in supporting hematopoiesis. Additionally, BM-MSCs tend to lose their functional ability after extended in vitro culture, which is necessary for producing sufficient cell numbers for clinical use. These limitations underscore the importance of pretreating MSCs with suitable signaling modulators to boost their functionality. Reliable in vitro assays play a crucial role in finding such signaling compounds and evaluating their effects on MSCs. Conventional assays, such as long-term-culture-initiating assay (LTC-IC assay) or colony-forming-unit assay (CFU assay), chemotactic migration assays (e.g., Transwell assay), etc., primarily evaluate the functional competence of HSCs and HSPCs, but provide little insight into the hematopoiesis-supportive capacity of MSCs. This chapter describes two such assays: one is designed to assess the hematopoietic stem/progenitor cell (HSPC)-supporting capacity of primed MSCs, and the other is specifically aimed at their ability to support the growth of primitive HSCs. These assays can serve as initial screens to test the impact, whether positive or negative, synergistic or antagonistic, of known signaling compounds, bioactive peptides, growth factors, and cytokines on MSC function or to discover new entities that could boost the functionality of MSCs.

Indexed as

Bone Marrow CellsMesenchymal Stem CellsSignal TransductionCell Culture TechniquesCell DifferentiationCells, CulturedColony-Forming Units AssayHematopoiesisHematopoietic Stem CellsHumansCD34Cell–cell interactionsCFU assayHematopoiesisHSCsHSPCsMSCsSignaling modulators

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.