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Exocytosis of large-diameter lysosomes mediates interferon γ-induced relocation of MHC class II molecules toward the surface of astrocytes
ID
Božić, Mićo
(
Avtor
),
ID
Verkhratsky, Alexei
(
Avtor
),
ID
Zorec, Robert
(
Avtor
),
ID
Stenovec, Matjaž
(
Avtor
)
PDF - Predstavitvena datoteka,
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(3,06 MB)
MD5: 70A3911DA2F86DD9148860B535EE6E00
URL - Izvorni URL, za dostop obiščite
https://rd.springer.com/article/10.1007%2Fs00018-019-03350-8
Galerija slik
Izvleček
Astrocytes are the key homeostatic cells in the central nervous system; initiation of reactive astrogliosis contributes to neuroinflammation. Pro-inflammatory cytokine interferon γ (IFNγ) induces the expression of the major histocompatibility complex class II (MHCII) molecules, involved in antigen presentation in reactive astrocytes. The pathway for MHCII delivery to the astrocyte plasma membrane, where MHCII present antigens, is unknown. Rat astrocytes in culture and in organotypic slices were exposed to IFNγ to induce reactive astrogliosis. Astrocytes were probed with optophysiologic tools to investigate subcellular localization of immunolabeled MHCII, and with electrophysiology to characterize interactions of single vesicles with the plasmalemma. In culture and in organotypic slices, IFNγ augmented the astrocytic expression of MHCII, which prominently co-localized with lysosomal marker LAMP1-EGFP, modestly co-localized with Rab7, and did not co-localize with endosomal markers Rab4A, EEA1, and TPC1. MHCII lysosomal localization was corroborated by treatment with the lysosomolytic agent glycyl-L-phenylalanine-β-naphthylamide, which reduced the number of MHCII-positive vesicles. The surface presence of MHCII was revealed by immunolabeling of live non-permeabilized cells. In IFNγ-treated astrocytes, an increased fraction of large-diameter exocytotic vesicles (lysosome-like vesicles) with prolonged fusion pore dwell time and larger pore conductance was recorded, whereas the rate of endocytosis was decreased. Stimulation with ATP, which triggers cytosolic calcium signaling, increased the frequency of exocytotic events, whereas the frequency of full endocytosis was further reduced. In IFNγ-treated astrocytes, MHCII-linked antigen surface presentation is mediated by increased lysosomal exocytosis, whereas surface retention of antigens is prolonged by concomitant inhibition of endocytosis.
Jezik:
Angleški jezik
Ključne besede:
astroglia
,
inflammatory cytokines
,
fusion pore
,
adaptive immunity
,
patch clamp
,
lysosomes
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2020
Št. strani:
Str. 3245-3264
Številčenje:
Vol. 77, iss. 16
PID:
20.500.12556/RUL-128778
UDK:
616-092
ISSN pri članku:
1420-682X
DOI:
10.1007/s00018-019-03350-8
COBISS.SI-ID:
34551513
Datum objave v RUL:
28.07.2021
Število ogledov:
903
Število prenosov:
167
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Cellular and molecular life sciences
Skrajšan naslov:
Cell Mol Life Sci
Založnik:
Birkhäuser
ISSN:
1420-682X
COBISS.SI-ID:
1615380
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:
01.08.2020
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
astroglia
,
vnetni citokini
,
fuzijske pore
,
adaptivna imunost
,
obliž
,
lizosomi
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P3-0310
Naslov:
Celična fiziologija
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
J3-6790
Naslov:
Dinamične meritve metabolitov in sekundarnih prenašalcev v posameznem astrocitu v celični kulturi
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
J3-9266
Naslov:
Uravnavanje fuzijske pore in motnje skladiščenja v lizosomih
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