Evidence map›Paper›PMID 41036675›Full record

ArticleCell biology international2025

Establishment, Characterization, and Cryopreservation of Feather Follicle Fibroblast Lines From Hyacinth Macaw (Anodorhynchus hyacinthinus).

Iara Pastor Martins Nogueira, Rachel Castro Teixeira-Santos, Gustavo Caldeira Cotta, Wanderson Valente, John Lennon Paiva de Coimbra, Heloísa Athaydes Seabra Ferreira, Pedro Pires Goulart Guimarães, Anderson Kenedy Santos, Fernanda Mussi Fontoura, Kefany Rodrigues de Andrade Ramalho and 2 more

Abstract read
In one paragraph

Article in Cell biology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Iara Pastor Martins NogueiraLaboratory of Cellular Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Rachel Castro Teixeira-SantosLaboratory of Cellular Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Gustavo Caldeira CottaLaboratory of Cellular Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Wanderson ValenteLaboratory of Cellular Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
John Lennon Paiva de CoimbraLaboratory of Cellular Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Heloísa Athaydes Seabra FerreiraSystems and Nanostructured Biophysics Laboratory, Department of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.ORCID https://orcid.org/0000-0002-5849-3245
Pedro Pires Goulart GuimarãesSystems and Nanostructured Biophysics Laboratory, Department of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Anderson Kenedy SantosGenetics Department, Yale School of Medicine, Yale University, New Haven, Connecticut, USA.ORCID https://orcid.org/0000-0002-6185-3491
Fernanda Mussi FontouraArara Azul Institute, Campo Grande, Mato Grosso do Sul, Brazil.
Kefany Rodrigues de Andrade RamalhoArara Azul Institute, Campo Grande, Mato Grosso do Sul, Brazil.
Neiva Maria Robaldo GuedesArara Azul Institute, Campo Grande, Mato Grosso do Sul, Brazil.
Samyra Maria Dos Santos Nassif LacerdaLaboratory of Cellular Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.ORCID https://orcid.org/0000-0003-4577-6243

Funding

This study was funded by FAPEMIG (Fundação de Amparo à Pesquisa do Estado de Minas Gerais), CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico), CAPES (Fundação Coordenação de Aperfeiçoamento de Pessoal de Nível Superior) and Fundação Toyota Brasil.
6 · The paper itself

Abstract

Cryopreservation, biobanking, and in vitro propagation of cells from endangered species represent key strategies for advancing biodiversity conservation. The Hyacinth Macaw (Anodorhynchus hyacinthinus), a flagship avian species of the Brazilian Pantanal, is among the critically vulnerable taxa that stand to benefit significantly from such cutting-edge biotechnological interventions. This study developed and validated minimally invasive methods for isolating, culturing, and cryopreserving fibroblasts derived from feather follicles (FFFs) of Hyacinth Macaws. Cells isolated from nestlings under 100 days of age demonstrated superior yields and viability compared to older birds. Two cryopreservation media were tested-Cryomedium 1 (55% DMEM-F12, 35% FBS, 10% DMSO) and Cryomedium 2 (90% FBS, 10% DMSO)-with Cryomedium 1 proving more effective in maintaining FFFs viability immediately post-thaw. Several culture conditions were evaluated, including conventional plating, drop plating, gelatin coating, and supplementation with RevitaCell and bFGF. The optimal method involved conventional plating on gelatin-coated plates with RevitaCell supplementation during the first 24 h post-thaw. Additionally, two different culture media were tested, with KAV-1 emerging as the best option for the long-term propagation of Hyacinth Macaw fibroblasts. After some passages, FFFs maintained a stable karyotype of 2n = 70, expressed classical fibroblast markers such as Vim, Fap, Acta2, Col1a1, Col1a2, synthesized vimentin and Type I collagen in the cytoplasm, and were confirmed to be free of mycoplasma contamination. We successfully established the first primary fibroblast cell lines derived from the Hyacinth Macaw and demonstrated their efficient responsiveness to lipid nanoparticle-mediated transfection and exogenous gene expression, representing a significant advancement toward the development of somatic reprogramming strategies. These experiments enabled the optimization of protocols for cell collection, cryopreservation, in vitro propagation, and inducing sustained heterologous expression, thereby laying a valuable foundation for the future generation of induced pluripotent stem cells (iPSCs) to support ex situ conservation efforts for this endangered species.

Indexed as

CryopreservationFeathersFibroblastsParrotsAnimalsCell Culture TechniquesCell LineCells, CulturedCell SurvivalAnodorhynchus Hyacinthinuscell culturecryopreservationfeather follicle fibroblasts (FFFs)Macaw

Identifiers

PMID41036675
PMCPMC12605831

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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.