Evidence map›Paper›PMID 41196134›Full record

ArticleTranslational vision science & technology2025

Two-Photon Fabrication of Donor-Specific Human Lamina Cribrosa Models.

Remi J Shittu, Brock Pemberton, Markus Boettcher, Jonathan P Vande Geest

Abstract read
In one paragraph

Article in Translational vision science & technology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

4 authors.

Remi J ShittuBioengineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, PA, USA.
Brock PembertonBioengineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, PA, USA.
Markus BoettcherMiltenyi Biotec B.V. and Co. KG, Bielefeld, Germany.
Jonathan P Vande GeestBioengineering, Swanson School of Engineering, University of Pittsburgh, Pittsburgh, PA, USA.

Funding

Interdisciplinary Visual Sciences (IVS) Traininig ProgramT32EY017271 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Marlene Behrmann, Paul R. Kinchington · 2008 to 2026
$3.6M
Extracelluar Matrix Organization and Biomechanics of the Lamina Cribrosa and Peripapillary Sclera in Populations at High Risk for Primary Open Angle GlaucomaR01EY020890 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VANDE GEEST, JONATHAN PIETER · 2011 to 2015
$1.8M
NEI NIH HHS R01 EY020890NEI NIH HHS T32 EY017271
6 · The paper itself

Abstract

Purpose: The lamina cribrosa (LC) is a complex network of collagenous beams that maintains mechanical homeostasis in response to fluctuations in intraocular pressure, thus protecting retinal ganglion cell axons exiting the eye. Understanding the structure and function of the LC may provide new insights into glaucomatous neurodegeneration. The purpose of this study is to utilize a two-photon fabrication technique to fabricate a model of the human LC (mLC) to scale. Methods: Segmented multiphoton microscopy images of human LC tissues from a prior study were used to two-photon polymerize three mLCs. The mLCs were subsequently imaged using micro-computed tomography. Regional and full-field structural anisotropies and global microstructure were compared between the input and micro-computed tomography mLC images. Results: Structural analysis of the LC tissues and mLCs demonstrates that various characteristics were closely maintained after fabrication. There was variation in the parameters across samples. Pore eccentricity, structural anisotropy, and pore convexity were all closely recapitulated with an error of less than approximately 15%. Conclusions: Generating a model of the human LC from segmented images is the first step toward a biomimetic approach to patient-specific modeling of the LC. Future work to improve the resolution and match the material properties of LC native tissues will generate a powerful model for mechanobiological studies. Mechanobiological experiments may be useful to understand the underlying mechanisms that drive glaucoma disease initiation and progression. Translational Relevance: This study introduces a novel method to fabricate the human LC, which can allow for patient-specific mechanobiological models of the LC in glaucoma.

Indexed as

GlaucomaMicroscopy, Fluorescence, MultiphotonOptic DiskHumansTissue DonorsX-Ray Microtomography

Identifiers

PMID41196134
PMCPMC12603958

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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.