Evidence map›Paper›PMID 35532208›Full record

ArticleJournal of biomedical materials research. Part B, Applied biomaterials2022

Native human collagen type I provides a viable physiologically relevant alternative to xenogeneic sources for tissue engineering applications: A comparative in vitro and in vivo study.

Tânia Baltazar, Nilabh S Kajave, Marco Rodriguez, Srija Chakraborty, Bo Jiang, Aleksander Skardal, Vipuil Kishore, Jordan S Pober, Mohammad Z Albanna

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part B, Applied biomaterials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. 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

9 authors at 5 institutions in 2 countries.

Tânia BaltazarDepartment of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0001-5071-5037
Nilabh S KajaveDepartment of Biomedical and Chemical Engineering and Sciences, Florida Institute of Technology, Melbourne, Florida, USA.
Marco RodriguezDepartment of Biomedical Engineering, The Ohio State University, Columbus, Ohio, USA.
Srija ChakrabortyDepartment of Biomedical Engineering, The Ohio State University, Columbus, Ohio, USA.
Bo JiangDepartment of Surgery, Yale University School of Medicine, New Haven, Connecticut, USA.
Aleksander SkardalDepartment of Biomedical Engineering, The Ohio State University, Columbus, Ohio, USA.
Vipuil KishoreDepartment of Biomedical and Chemical Engineering and Sciences, Florida Institute of Technology, Melbourne, Florida, USA.
Jordan S PoberDepartment of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA.
Mohammad Z AlbannaHumabiologics Inc, Phoenix, Arizona, USA.ORCID 0000-0002-7291-0033
Yale University · USFlorida Institute of Technology · USThe Ohio State University · USAtrium Health Wake Forest Baptist · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · US

Funding

Optimizing Therapeutic Revascularization by Endothelial Cell TransplantationR01HL085416 · NHLBI · YALE UNIVERSITY · PI POBER, JORDAN S, SALTZMAN, W. MARK · 2006 to 2019
$5.9M
3D Printed Biomimetic Bioglass-Gradient Matrices for ACL ReconstructionR15AR071102 · NIAMS · FLORIDA INSTITUTE OF TECHNOLOGY · PI KISHORE, VIPUIL · 2017 to 2023
$827k
Assessment of immunogenicity and antigenicity of different human cell types in natural and 3D-printed allograftsR21AI159580 · NIAID · YALE UNIVERSITY · PI POBER, JORDAN S · 2021 to 2022
$461k
NHLBI NIH HHS R01 HL085416NIAID NIH HHS R21 AI159580NIAMS NIH HHS R15 AR071102
6 · The paper itself

Abstract

Xenogeneic sources of collagen type I remain a common choice for regenerative medicine applications due to ease of availability. Human and animal sources have some similarities, but small variations in amino acid composition can influence the physical properties of collagen, cellular response, and tissue remodeling. The goal of this work is to compare human collagen type I-based hydrogels versus animal-derived collagen type I-based hydrogels, generated from commercially available products, for their physico-chemical properties and for tissue engineering and regenerative medicine applications. Specifically, we evaluated whether the native human skin type I collagen could be used in the three most common research applications of this protein: as a substrate for attachment and proliferation of conventional 2D cell culture; as a source of matrix for a 3D cell culture; and as a source of matrix for tissue engineering. Results showed that species and tissue specific variations of collagen sources significantly impact the physical, chemical, and biological properties of collagen hydrogels including gelation kinetics, swelling ratio, collagen fiber morphology, compressive modulus, stability, and metabolic activity of hMSCs. Tumor constructs formulated with human skin collagen showed a differential response to chemotherapy agents compared to rat tail collagen. Human skin collagen performed comparably to rat tail collagen and enabled assembly of perfused human vessels in vivo. Despite differences in collagen manufacturing methods and supplied forms, the results suggest that commercially available human collagen can be used in lieu of xenogeneic sources to create functional scaffolds, but not all sources of human collagen behave similarly. These factors must be considered in the development of 3D tissues for drug screening and regenerative medicine applications.

Indexed as

Collagen Type ITissue EngineeringAnimalsCollagenExtracellular MatrixHumansHydrogelsRatsTissue ScaffoldsCollagenCollagen Type IHydrogels3D constructcancer modelingcollagen type Ihydrogelxeno

Identifiers

PMID35532208
PMCPMC11103545
OpenAlexW4229365980

What OpenQuestion holds

Textmetadata
LicenceTDM
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.