» Articles » PMID: 34057729

Manufacturing a Bone Marrow-On-A-Chip Using Maskless Photolithography

Overview
Specialty Molecular Biology
Date 2021 May 31
PMID 34057729
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

The bone marrow (BM) is a complex microenvironment in which hematopoietic stem and progenitor cells (HSPCs) interact with multiple cell types that regulate their quiescence, growth, and differentiation. These cells constitute local niches where HSPCs are confined and subjected to specific set of physical and biochemical cues. Endothelial cells forming the walls of blood capillaries have been shown to establish a vascular niche, whereas osteoblasts lying along the bone matrix organize the endosteal niche with distinct and specific impact on HSPC fate. The observation of the interaction of HSPCs with niche cells, and the investigation of its impact on HSPCs behavior in vivo is hindered by the opacity of the bone matrix. Therefore, various experimental strategies have been devised to reconstitute in vitro the interaction of HSPCs with distinct sets of BM-derived cells. In this chapter, we present a method to manufacture a pseudo BM-on-a-chip with separated compartments mimicking the vascular and the endosteal niches. Such a configuration with connected but distant compartments allowed the investigation of the specific contribution of each niche to the regulation of HSPC behavior. We describe the microfabrication of the chip with a maskless photolithography method that allows the iterative improvement of the geometric design of the chip in order to optimize the adaptation of the multicellular architecture to the specific aim of the study. We also describe the loading and culture of the various cell types in each compartment.

Citing Articles

Why Animal Experiments Are Still Indispensable in Bone Research: A Statement by the European Calcified Tissue Society.

Stein M, Elefteriou F, Busse B, Fiedler I, Kwon R, Farrell E J Bone Miner Res. 2023; 38(8):1045-1061.

PMID: 37314012 PMC: 10962000. DOI: 10.1002/jbmr.4868.


Organoids and microphysiological systems: Promising models for accelerating AAV gene therapy studies.

Ramamurthy R, Atala A, Porada C, Almeida-Porada G Front Immunol. 2022; 13:1011143.

PMID: 36225917 PMC: 9549755. DOI: 10.3389/fimmu.2022.1011143.


Bone Marrow Niches of Hematopoietic Stem and Progenitor Cells.

Kandarakov O, Belyavsky A, Semenova E Int J Mol Sci. 2022; 23(8).

PMID: 35457280 PMC: 9032554. DOI: 10.3390/ijms23084462.


Rapid Prototyping of Organ-on-a-Chip Devices Using Maskless Photolithography.

Kasi D, de Graaf M, Motreuil-Ragot P, Frimat J, Ferrari M, Sarro P Micromachines (Basel). 2022; 13(1).

PMID: 35056214 PMC: 8778126. DOI: 10.3390/mi13010049.


Hematopoietic progenitors polarize in contact with bone marrow stromal cells in response to SDF1.

Bessy T, Candelas A, Souquet B, Saadallah K, Schaeffer A, Vianay B J Cell Biol. 2021; 220(11).

PMID: 34570198 PMC: 8479938. DOI: 10.1083/jcb.202005085.

References
1.
Velten L, Haas S, Raffel S, Blaszkiewicz S, Islam S, Hennig B . Human haematopoietic stem cell lineage commitment is a continuous process. Nat Cell Biol. 2017; 19(4):271-281. PMC: 5496982. DOI: 10.1038/ncb3493. View

2.
Morrison S, Scadden D . The bone marrow niche for haematopoietic stem cells. Nature. 2014; 505(7483):327-34. PMC: 4514480. DOI: 10.1038/nature12984. View

3.
Pinho S, Frenette P . Haematopoietic stem cell activity and interactions with the niche. Nat Rev Mol Cell Biol. 2019; 20(5):303-320. PMC: 6483843. DOI: 10.1038/s41580-019-0103-9. View

4.
Sanchez-Aguilera A, Mendez-Ferrer S . The hematopoietic stem-cell niche in health and leukemia. Cell Mol Life Sci. 2016; 74(4):579-590. PMC: 5272896. DOI: 10.1007/s00018-016-2306-y. View

5.
Verovskaya E, Dellorusso P, Passegue E . Losing Sense of Self and Surroundings: Hematopoietic Stem Cell Aging and Leukemic Transformation. Trends Mol Med. 2019; 25(6):494-515. PMC: 7657013. DOI: 10.1016/j.molmed.2019.04.006. View