Supporting data of spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo

Gustavo Higuera Sierra, Hugo Fernandes, Tim Spitters, Jeroen van de Peppel, Nils Auffermann, Roman Truckenmüller, Maryana Escalante, Reinout Stoop, Johannes P. van Leeuwen, Jan de Boer, Vinod Subramaniam, Marcel Karperien, Clemens van Blitterswijk, Anton van Boxtel, Lorenzo Moroni

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

This data article contains seven figures and two tables supporting the research article entitled: spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo[1]. The data explain the culture of stromal cells in vitro in three culture systems: discs, scaffolds and scaffolds in a perfusion bioreactor system. Also, quantification of extracellular matrix components (ECM) in vitro and staining of ECM components in vivo can be found here. Finally the quantification of blood vessels dimensions from CD31 signals and representative histograms of stanniocalcin-1 fluorescent signals in negative controls and experimental conditions in vivo are presented.
Original languageEnglish
Pages (from-to)84-94
JournalData in brief
Volume5
DOIs
Publication statusPublished - 28 Aug 2015

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Stromal Cells
Food
Extracellular Matrix
Bioreactors
Blood Vessels
Perfusion
Staining and Labeling
Research
In Vitro Techniques
teleocalcin

Keywords

  • METIS-313709
  • IR-98547

Cite this

Higuera Sierra, Gustavo ; Fernandes, Hugo ; Spitters, Tim ; van de Peppel, Jeroen ; Auffermann, Nils ; Truckenmüller, Roman ; Escalante, Maryana ; Stoop, Reinout ; van Leeuwen, Johannes P. ; de Boer, Jan ; Subramaniam, Vinod ; Karperien, Marcel ; van Blitterswijk, Clemens ; van Boxtel, Anton ; Moroni, Lorenzo. / Supporting data of spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo. In: Data in brief. 2015 ; Vol. 5. pp. 84-94.
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title = "Supporting data of spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo",
abstract = "This data article contains seven figures and two tables supporting the research article entitled: spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo[1]. The data explain the culture of stromal cells in vitro in three culture systems: discs, scaffolds and scaffolds in a perfusion bioreactor system. Also, quantification of extracellular matrix components (ECM) in vitro and staining of ECM components in vivo can be found here. Finally the quantification of blood vessels dimensions from CD31 signals and representative histograms of stanniocalcin-1 fluorescent signals in negative controls and experimental conditions in vivo are presented.",
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author = "{Higuera Sierra}, Gustavo and Hugo Fernandes and Tim Spitters and {van de Peppel}, Jeroen and Nils Auffermann and Roman Truckenm{\"u}ller and Maryana Escalante and Reinout Stoop and {van Leeuwen}, {Johannes P.} and {de Boer}, Jan and Vinod Subramaniam and Marcel Karperien and {van Blitterswijk}, Clemens and {van Boxtel}, Anton and Lorenzo Moroni",
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Higuera Sierra, G, Fernandes, H, Spitters, T, van de Peppel, J, Auffermann, N, Truckenmüller, R, Escalante, M, Stoop, R, van Leeuwen, JP, de Boer, J, Subramaniam, V, Karperien, M, van Blitterswijk, C, van Boxtel, A & Moroni, L 2015, 'Supporting data of spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo' Data in brief, vol. 5, pp. 84-94. https://doi.org/10.1016/j.dib.2015.08.012

Supporting data of spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo. / Higuera Sierra, Gustavo; Fernandes, Hugo; Spitters, Tim; van de Peppel, Jeroen; Auffermann, Nils; Truckenmüller, Roman; Escalante, Maryana; Stoop, Reinout; van Leeuwen, Johannes P.; de Boer, Jan; Subramaniam, Vinod; Karperien, Marcel; van Blitterswijk, Clemens; van Boxtel, Anton; Moroni, Lorenzo.

In: Data in brief, Vol. 5, 28.08.2015, p. 84-94.

Research output: Contribution to journalArticleAcademicpeer-review

TY - JOUR

T1 - Supporting data of spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo

AU - Higuera Sierra, Gustavo

AU - Fernandes, Hugo

AU - Spitters, Tim

AU - van de Peppel, Jeroen

AU - Auffermann, Nils

AU - Truckenmüller, Roman

AU - Escalante, Maryana

AU - Stoop, Reinout

AU - van Leeuwen, Johannes P.

AU - de Boer, Jan

AU - Subramaniam, Vinod

AU - Karperien, Marcel

AU - van Blitterswijk, Clemens

AU - van Boxtel, Anton

AU - Moroni, Lorenzo

PY - 2015/8/28

Y1 - 2015/8/28

N2 - This data article contains seven figures and two tables supporting the research article entitled: spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo[1]. The data explain the culture of stromal cells in vitro in three culture systems: discs, scaffolds and scaffolds in a perfusion bioreactor system. Also, quantification of extracellular matrix components (ECM) in vitro and staining of ECM components in vivo can be found here. Finally the quantification of blood vessels dimensions from CD31 signals and representative histograms of stanniocalcin-1 fluorescent signals in negative controls and experimental conditions in vivo are presented.

AB - This data article contains seven figures and two tables supporting the research article entitled: spatiotemporal proliferation of human stromal cells adjusts to nutrient availability and leads to stanniocalcin-1 expression in vitro and in vivo[1]. The data explain the culture of stromal cells in vitro in three culture systems: discs, scaffolds and scaffolds in a perfusion bioreactor system. Also, quantification of extracellular matrix components (ECM) in vitro and staining of ECM components in vivo can be found here. Finally the quantification of blood vessels dimensions from CD31 signals and representative histograms of stanniocalcin-1 fluorescent signals in negative controls and experimental conditions in vivo are presented.

KW - METIS-313709

KW - IR-98547

U2 - 10.1016/j.dib.2015.08.012

DO - 10.1016/j.dib.2015.08.012

M3 - Article

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SP - 84

EP - 94

JO - Data in brief

JF - Data in brief

SN - 2352-3409

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