A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
Sodium channels enable fast electrical signaling and regulate phagocytosis in the retinal pigment epithelium (2019)
Johansson, J. K., Karema-Jokinen, V. I., Hakanen, S., Jylhä, A., Uusitalo, H., Vihinen-Ranta, M., Skottman, H., Ihalainen, T. O., & Nymark, S. (2019). Sodium channels enable fast electrical signaling and regulate phagocytosis in the retinal pigment epithelium. BMC Biology, 17, Article 63. https://doi.org/10.1186/s12915-019-0681-1
JYU-tekijät tai -toimittajat
Julkaisun tiedot
Julkaisun kaikki tekijät tai toimittajat: Johansson, Julia K.; Karema-Jokinen, Viivi I.; Hakanen, Satu; Jylhä, Antti; Uusitalo, Hannu; Vihinen-Ranta, Maija; Skottman, Heli; Ihalainen, Teemu O.; Nymark, Soile
Lehti tai sarja: BMC Biology
eISSN: 1741-7007
Julkaisuvuosi: 2019
Volyymi: 17
Artikkelinumero: 63
Kustantaja: BioMed Central Ltd.
Julkaisumaa: Britannia
Julkaisun kieli: englanti
DOI: https://doi.org/10.1186/s12915-019-0681-1
Julkaisun avoin saatavuus: Avoimesti saatavilla
Julkaisukanavan avoin saatavuus: Kokonaan avoin julkaisukanava
Julkaisu on rinnakkaistallennettu (JYX): https://jyx.jyu.fi/handle/123456789/65292
Tiivistelmä
Voltage-gated sodium (Nav) channels have traditionally been considered a trademark of excitable cells. However, recent studies have shown the presence of Nav channels in several non-excitable cells, such as astrocytes and macrophages, demonstrating that the roles of these channels are more diverse than was previously thought. Despite the earlier discoveries, the presence of Nav channel-mediated currents in the cells of retinal pigment epithelium (RPE) has been dismissed as a cell culture artifact. We challenge this notion by investigating the presence and possible role of Nav channels in RPE both ex vivo and in vitro.
Results
Our work demonstrates that several subtypes of Nav channels are found in human embryonic stem cell (hESC)-derived and mouse RPE, most prominently subtypes Nav1.4, Nav1.6, and Nav1.8. Whole cell patch clamp recordings from the hESC-derived RPE monolayers showed that the current was inhibited by TTX and QX-314 and was sensitive to the selective blockers of the main Nav subtypes. Importantly, we show that the Nav channels are involved in photoreceptor outer segment phagocytosis since blocking their activity significantly reduces the efficiency of particle internalization. Consistent with this role, our electron microscopy results and immunocytochemical analysis show that Nav1.4 and Nav1.8 accumulate on phagosomes and that pharmacological inhibition of Nav channels as well as silencing the expression of Nav1.4 with shRNA impairs the phagocytosis process.
Conclusions
Taken together, our study shows that Nav channels are present in RPE, giving this tissue the capacity of fast electrical signaling. The channels are critical for the physiology of RPE with an important role in photoreceptor outer segment phagocytosis.
YSO-asiasanat: proteiinit; soluviestintä; fagosytoosi; aistinreseptorit; verkkokalvo
Vapaat asiasanat: RPE; ion channels; Nav; patch clamp; phagocytosis; retina; photoreceptors
Liittyvät organisaatiot
Hankkeet, joissa julkaisu on tehty
- Herpes virusten toiminta solun tumassa
- Vihinen-Ranta, Maija
- Jane ja Aatos Erkon säätiö
- Herpesvirusten kulkeutuminen isäntäsolun tumassa
- Vihinen-Ranta, Maija
- Jane ja Aatos Erkon säätiö
OKM-raportointi: Kyllä
Raportointivuosi: 2019
JUFO-taso: 2