Mata, G. | bioRxiv Science

bioRxiv2024

Laser Scanning Confocal printing, a new simple method for micro-device fabrication (LSCprint method).

Micro-devices and lab-on-a-chip technologies have revolutionized cell biology research, enabling a plethora of applications from single-cell sorting to organ-on-a-chip assays. However, their construction remains laborious, requiring specialized equipment and trained personnel, thereby restricting their accessibility to specialized laboratories. The conventional protocol for micro-device printing involves intricate steps, including master cast/mold production and device fabrication, leading to high costs and time consumption. Here, we present a novel, simplified method utilizing a laser scanning confocal microscope (LSCM) and commercially available photosensitive resins. By using the UV or violet excitation laser lines of an LSCM, we eliminate the need for external suppliers and complex equipment, enabling any conventional cell biology laboratory to fabricate micro-devices swiftly and inexpensively. Our method not only enhances the capabilities of standard confocal microscopes but also democratises microfluidic device fabrication, making it accessible to non-specialized laboratories. With minimal reagent consumption and high scalability, our approach offers a cost-effective solution for rapid prototyping and production of micro-devices, circumventing previous barriers to widespread adoption. Moreover, our method allows direct printing of micro-devices onto substrates, eliminating the need for molds and intermediate steps, thus facilitating greater design flexibility and accessibility for non-specialized laboratories.

bioengineering↗

bioRxiv2023

The nucleolar aberrancies that drive ribosome impairment induced by RNA binding proteins are hallmarks of aging

The nucleolus is a dynamic structure where ribosome subunits are produced. Indeed, nucleoli respond to any change in cellular homeostasis by altering the rate of ribosome biogenesis, thus working as a stress sensor. Therefore, an imbalance in ribosome biogenesis promotes changes in morphology and function and can evoke a nucleolar stress response. Changes in the structure and composition of nucleoli impair ribosome biogenesis and have been described as nucleolar stress, a mechanism related to aging and cancer. Here, we show the role of the RNA binding protein Hnrnpk in nucleolar dynamics and ribosome function. Hnrnpk is a ribonucleoprotein in charge of escorting nascent transcripts to its processing and nuclear export to ribosomes. When Hnrnpk is overexpressed, the nucleolus is altered and shows stress-like phenotype, with accumulation and delocalization of components such as Ncl, driving ribosome biogenesis impairment and halting protein translation. Nucleolin haploinsufficiency is correlated with enlarged nucleoli, increased ribosome components and translation and induces a reduction in lifespan. Thus, gain of Ncl generated by Hnrnpk overexpression can cause ribosome biogenesis defects associated with ribosome impairment leading to ribosomopathies and bone marrow failure syndrome. Aging and bone marrow failure share common biological hallmarks. Indeed, Hnrnpk overexpression and nucleolar stress trigger cell cycle arrest and senescence of the cells, a feature of both processes. Together, these findings support the idea that nucleolar abnormalities contribute to ribosome impairment, thus triggering the onset of hematopoiesis and the aging process. Here, we decipher a novel master regulator of this mechanism: Hnrnpk.

molecular biology↗