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Updated: Aug 20, 2026

Microengineering 3D Collagen Hydrogels with Long-Range Fiber Alignment
Published on: September 7, 2022
Modeled microgravity disrupts collagen I/integrin signaling during osteoblastic differentiation of human mesenchymal
Valerie E Meyers1, Maid Zayzafoon, Steve R Gonda
1Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Abstract:
Spaceflight leads to reduced bone mineral density in weight bearing bones that is primarily attributed to a reduction in bone formation. We have previously demonstrated severely reduced osteoblastogenesis of human mesenchymal stem cells (hMSC) following 7 days culture in modeled microgravity (MMG). One potential mechanism for reduced osteoblastic differentiation is disruption of type I collagen (Col I)-integrin interactions and reduced integrin signaling. Integrins are heterodimeric transmembrane receptors that bind extracellular matrix (ECM) proteins and produce signals essential for proper cellular function, survival, and differentiation. Therefore, we investigated the effects of MMG on integrin expression and function in hMSC. We demonstrate that 7 days of culture in MMG leads to reduced expression of the ECM protein, Col I. Conversely, MMG consistently increases Col I-specific alpha2 and beta1 integrin protein expression. Despite this increase in integrin subunit expression, autophosphorylation of adhesion-dependent kinases, focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (PYK2), is significantly reduced. Activation of Akt protein kinase (Akt) is unaffected by the reduction in FAK activation. However, reduced downstream signaling via the Ras-mitogen activated protein kinase (MAPK) pathway is evidenced by a reduction in Ras and extracellular signal-related protein kinase (ERK) activation. Taken together, our findings indicate that MMG decreases integrin/MAPK signaling, which likely contributes to the observed reduction in osteoblastogenesis.
Insights
Spaceflight reduces bone formation by disrupting cell signaling. Modeled microgravity (MMG) decreases type I collagen and integrin signaling, impairing osteoblast differentiation crucial for bone health.
Area of Science:
- Space biology
- Cell biology
- Biochemistry
Background:
- Spaceflight causes bone loss, primarily due to reduced bone formation.
- Human mesenchymal stem cells (hMSC) show reduced osteoblastogenesis in modeled microgravity (MMG).
- Disrupted type I collagen (Col I)-integrin interactions may impair osteoblastic differentiation.
Purpose of the Study:
- Investigate the effects of MMG on integrin expression and signaling in hMSC.
- Determine how MMG affects key signaling pathways involved in osteoblast differentiation.
Main Methods:
- Cultured hMSC in MMG for 7 days.
- Analyzed expression of Col I, alpha2, and beta1 integrins.
- Assessed phosphorylation of focal adhesion kinase (FAK), proline-rich tyrosine kinase 2 (PYK2), Akt, Ras, and extracellular signal-related kinase (ERK).
Main Results:
- MMG decreased Col I expression but increased alpha2 and beta1 integrin expression.
- MMG significantly reduced FAK and PYK2 autophosphorylation.
- MMG reduced Ras and ERK activation, indicating impaired MAPK signaling.
- Akt activation remained unaffected.
Conclusions:
- MMG disrupts integrin-mediated signaling pathways in hMSC.
- Reduced integrin/MAPK signaling likely contributes to decreased osteoblastogenesis observed in microgravity.
- Findings provide insights into cellular mechanisms of spaceflight-induced bone loss.

