Evidence map›Paper›PMID 38504086›Full record

ArticleIn vitro cellular & developmental biology. Animal2024

The molecular mechanisms underlying the regeneration process in the earthworm, Perionyx excavatus exhibit indications of apoptosis-induced compensatory proliferation (AICP).

Kamarajan Rajagopalan, Jackson Durairaj Selvan Christyraj, Karthikeyan Subbiahanadar Chelladurai, Johnson Retnaraj Samuel Selvan Christyraj, Puja Das, Apoorva Roy, Chaughule Vrushali, Nehla Siraj M Chemmet

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In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 23% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. DNA Methylation Dynamics inBiomolecules · 2026
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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

8 authors at 2 institutions in 1 country.

Kamarajan RajagopalanMolecular Biology and Stem Cell Biology Lab, Centre for Molecular and Nanomedical Sciences, International Research Centre, Sathyabama Institute of Science and Technology (Deemed to Be University), Jeppiaar Nagar, SH 49A, Chennai, Tamil Nadu, 621306, India.
Jackson Durairaj Selvan ChristyrajMolecular Biology and Stem Cell Biology Lab, Centre for Molecular and Nanomedical Sciences, International Research Centre, Sathyabama Institute of Science and Technology (Deemed to Be University), Jeppiaar Nagar, SH 49A, Chennai, Tamil Nadu, 621306, India. jacksondurairaj@sathyabama.ac.in.ORCID http://orcid.org/0000-0003-0363-0529
Karthikeyan Subbiahanadar ChelladuraiMolecular Biology and Stem Cell Biology Lab, Centre for Molecular and Nanomedical Sciences, International Research Centre, Sathyabama Institute of Science and Technology (Deemed to Be University), Jeppiaar Nagar, SH 49A, Chennai, Tamil Nadu, 621306, India.
Johnson Retnaraj Samuel Selvan ChristyrajMolecular Biology and Stem Cell Biology Lab, Centre for Molecular and Nanomedical Sciences, International Research Centre, Sathyabama Institute of Science and Technology (Deemed to Be University), Jeppiaar Nagar, SH 49A, Chennai, Tamil Nadu, 621306, India. johnnbt@sathyabama.ac.in.
Puja DasMolecular Biology and Stem Cell Biology Lab, Centre for Molecular and Nanomedical Sciences, International Research Centre, Sathyabama Institute of Science and Technology (Deemed to Be University), Jeppiaar Nagar, SH 49A, Chennai, Tamil Nadu, 621306, India.
Apoorva RoyDepartment of Biotechnology, Alagappa University, Karaikudi, Tamil Nadu, India.
Chaughule VrushaliDepartment of Biotechnology, Alagappa University, Karaikudi, Tamil Nadu, India.
Nehla Siraj M ChemmetDepartment of Biotechnology, Alagappa University, Karaikudi, Tamil Nadu, India.
Sathyabama Institute of Science and Technology · INAlagappa University · IN

Funding

DST-SHRI DST/TDT/SHRI-24/2021 (G)
6 · The paper itself

Abstract

Regeneration is a multifaceted biological phenomenon that necessitates the intricate orchestration of apoptosis, stem cells, and immune responses, culminating in the regulation of apoptosis-induced compensatory proliferation (AICP). The AICP context of research is observed in many animal models like in Hydra, Xenopus, newt, Drosophila, and mouse but so far not reported in earthworm. The earthworm Perionyx excavatus is used in the present study to understand the relationship between AICP-related protein expression and regeneration success in different conditions (normal regeneration and abnormal multiple bud formation). Initially, the worms are amputated into five equal portions and it is revealed that regeneration in P. excavatus is clitellum independent and it gives more preference for anterior regeneration (regrowth of head portion) than for posterior regeneration (regrowth of tail portion). The posterior segments of the worm possess enormous regeneration ability but this is lacking in anterior segments. Alkaline phosphate, a stem cell marker, shows strong signals throughout all the posterior segments but it decreases in the initial 1st to 15th anterior segments which lack the regeneration ability. While regenerating normally, it was suggested that the worm follow AICP principles. This is because there was increased expression of apoptosis signals throughout the regeneration process along with constant expression of stem cell proliferation response together with cellular proliferation. In amputated posterior segments maintained in vitro, the apoptosis signals were extensively detected on the 1st day. However, on the 4th and 6th days, caspase-3 and H2AX expression are significantly suppressed, which may eventually alter the Wnt3a and histone H3 patterns that impair the AICP and result in multiple bud formation. Our results suggest that AICP-related protein expression pattern is crucial for initiating proper regeneration.

Indexed as

OligochaetaAnimalsApoptosisCell ProliferationMiceApoptosis-induced compensatory proliferationH2AXP. excavatusRegenerationWnt3a

Identifiers

PMID38504086
OpenAlexW4392936549

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.