Evidence map›Paper›PMID 42618956›Full record

ReviewJournal of animal science and biotechnology2026

Developmental Cellular Programming: stage-specific architecting muscle and adipose tissues for high-quality meat production.

Bo Wang

Abstract readReview
In one paragraph

Review in Journal of animal science and biotechnology, 2026. 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.

Bo WangState Key Laboratory of Animal Nutrition and Feeding, College of Animal Science and Technology, China Agricultural University, Beijing, 100193, PR China. wangbo123@cau.edu.cn.ORCID https://orcid.org/0000-0003-0604-1607

Funding

National Natural Science Foundation of China 32272892
6 · The paper itself

Abstract

The rising global demand for animal protein has driven intensive selection for rapid growth and leanness, often at the expense of meat quality and animal health. Achieving high-quality meat production with optimal intramuscular fat (IMF) and superior myofiber characteristics remains a major challenge in animal agriculture. Here, we propose a holistic conceptual framework termed Developmental Cellular Programming (DCP), which utilizes distinct developmental windows to precisely regulate skeletal muscle and adipose tissue formation in meat animals. Unlike traditional late-stage finishing strategies, the DCP framework operates as a coordinated, stage-specific pipeline: optimizing maternal nutrition during gestation to maximize prenatal myofiber hyperplasia and initiate adipocyte lineages; executing targeted neonatal interventions to drive microenvironment-mediated adipogenic precursor expansion and angiogenesis; and fine-tuning nutrient allocation during the finishing phase to control cellular hypertrophy and lipid deposition. Within this framework, vascularization is established as a critical, shared control point that coordinates multi-tissue niches to synchronize myofiber and adipocyte development. While advanced three-dimensional cell culture models, such as vascularized tissue organoids, have emerged as powerful platforms for high-throughput screening of key candidate metabolic modulators, bridging the gap to livestock production necessitates translating these cellular responses into whole-animal phenotypes. We propose that future research should focus on conducting in vivo animal trials to elucidate how various nutrients regulate muscle and adipose cell differentiation at specific developmental stages, thereby establishing precision nutritional strategies based on the DCP theory for high-quality meat production.

Indexed as

Developmental programmingIntramuscular fatMeat qualityMuscle

Identifiers

PMID42618956
PMCPMC13487922

What OpenQuestion holds

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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.