Evidence map›Paper›PMID 31214600›Full record

ReviewFrontiers in cardiovascular medicine2019

Functional Vascular Tissue Engineering Inspired by Matricellular Proteins.

Aneesh K Ramaswamy, David A Vorp, Justin S Weinbaum

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Loss of MFAP5 and Its Effect on Skin Homeostasis and Wound Healing.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  2. Review
  3. Review
  4. Review
  5. Engineering Three-Dimensional Vascularized Cardiac Tissues.Tissue engineering. Part B, Reviews · 2022
    Review
  6. Matricellular proteins in cutaneous wound healing.Frontiers in cell and developmental biology · 2022
    Review
  7. Article
  8. Article
  9. Review
  10. Extracellular Matrix Patches for Endarterectomy Repair.Frontiers in cardiovascular medicine · 2021
    Article
  11. Bioactivity effects of extracellular matrix proteins on apical papilla cells.Journal of applied oral science : revista FOB · 2021
    Article
  12. Emerging Roles of Matricellular Proteins in Systemic Sclerosis.International journal of molecular sciences · 2020
    Review
  13. Review
  14. Article
  15. 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

3 authors at 2 institutions in 1 country.

Aneesh K RamaswamyDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States.
David A VorpDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States.
Justin S WeinbaumDepartment of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States.
University of Pittsburgh · USMcGowan Institute for Regenerative Medicine · US

Funding

Artificial Stem Cells for Vascular Tissue EngineeringR01HL130077 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VORP, DAVID ALAN · 2016 to 2019
$1.5M
Angiopathy Training GrantT32HL094295 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MARS, WENDY MICHELLE · 2010 to 2014
$1.2M
Outside-In Regenerative Therapy for Abdominal Aortic AneurysmR21HL129066 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CURCI, JOHN A, VORP, DAVID ALAN · 2015 to 2016
$439k
An Autologous, Culture-Free, Adipose Cell-Based Tissue Engineered Vascular GraftR21HL130784 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VORP, DAVID ALAN · 2016 to 2017
$418k
Improving fibrin-based bioartificial arteries by prolonging ERK activationF32HL104768 · NHLBI · UNIVERSITY OF MINNESOTA · PI WEINBAUM, JUSTIN SOL · 2011 to 2013
$124k
NHLBI NIH HHS F32 HL104768NHLBI NIH HHS R01 HL130077NHLBI NIH HHS R21 HL129066NHLBI NIH HHS R21 HL130784NHLBI NIH HHS T32 HL094295
6 · The paper itself

Abstract

Modern regenerative medicine, and tissue engineering specifically, has benefited from a greater appreciation of the native extracellular matrix (ECM). Fibronectin, collagen, and elastin have entered the tissue engineer's toolkit; however, as fully decellularized biomaterials have come to the forefront in vascular engineering it has become apparent that the ECM is comprised of more than just fibronectin, collagen, and elastin, and that cell-instructive molecules known as matricellular proteins are critical for desired outcomes. In brief, matricellular proteins are ECM constituents that contrast with the canonical structural proteins of the ECM in that their primary role is to interact with the cell. Of late, matricellular genes have been linked to diseases including connective tissue disorders, cardiovascular disease, and cancer. Despite the range of biological activities, this class of biomolecules has not been actively used in the field of regenerative medicine. The intent of this review is to bring matricellular proteins into wider use in the context of vascular tissue engineering. Matricellular proteins orchestrate the formation of new collagen and elastin fibers that have proper mechanical properties-these will be essential components for a fully biological small diameter tissue engineered vascular graft (TEVG). Matricellular proteins also regulate the initiation of thrombosis via fibrin deposition and platelet activation, and the clearance of thrombus when it is no longer needed-proper regulation of thrombosis will be critical for maintaining patency of a TEVG after implantation. Matricellular proteins regulate the adhesion, migration, and proliferation of endothelial cells-all are biological functions that will be critical for formation of a thrombus-resistant endothelium within a TEVG. Lastly, matricellular proteins regulate the adhesion, migration, proliferation, and activation of smooth muscle cells-proper control of these biological activities will be critical for a TEVG that recellularizes and resists neointimal formation/stenosis. We review all of these functions for matricellular proteins here, in addition to reviewing the few studies that have been performed at the intersection of matricellular protein biology and vascular tissue engineering.

Indexed as

collagenelastinendothelial cellsextracellular matrixsmooth muscle cellsthrombosis

Identifiers

PMID31214600
PMCPMC6554335
OpenAlexW2947510664

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.