• Je něco špatně v tomto záznamu ?

Zebrafish macrophage developmental arrest underlies depletion of microglia and reveals Csf1r-independent metaphocytes

LE. Kuil, N. Oosterhof, G. Ferrero, T. Mikulášová, M. Hason, J. Dekker, M. Rovira, HC. van der Linde, PM. van Strien, E. de Pater, G. Schaaf, EM. Bindels, V. Wittamer, TJ. van Ham

. 2020 ; 9 (-) : . [pub] 20200505

Jazyk angličtina Země Velká Británie

Typ dokumentu časopisecké články, práce podpořená grantem, audiovizuální média

Perzistentní odkaz   https://www.medvik.cz/link/bmc21012611

Grantová podpora
WELBIO-CR-2015S-04 WELBIO - International
322368 Marie Curie - United Kingdom
VENI 016.136.150 ZonMw - Netherlands
F451218F Fonds de la Recherche Scientifique FNRS under Incentive Grant for Scientific Research - International
18-18363S Czech Science Foundation - International
University Fellowship Erasmus University Rotterdam - International
322368 Marie Curie Career Integration Grant - International
F451218F Fonds De La Recherche Scientifique - FNRS - International

Macrophages derive from multiple sources of hematopoietic progenitors. Most macrophages require colony-stimulating factor 1 receptor (CSF1R), but some macrophages persist in the absence of CSF1R. Here, we analyzed mpeg1:GFP-expressing macrophages in csf1r-deficient zebrafish and report that embryonic macrophages emerge followed by their developmental arrest. In larvae, mpeg1+ cell numbers then increased showing two distinct types in the skin: branched, putative Langerhans cells, and amoeboid cells. In contrast, although numbers also increased in csf1r-mutants, exclusively amoeboid mpeg1+ cells were present, which we showed by genetic lineage tracing to have a non-hematopoietic origin. They expressed macrophage-associated genes, but also showed decreased phagocytic gene expression and increased epithelial-associated gene expression, characteristic of metaphocytes, recently discovered ectoderm-derived cells. We further demonstrated that juvenile csf1r-deficient zebrafish exhibit systemic macrophage depletion. Thus, csf1r deficiency disrupts embryonic to adult macrophage development. Zebrafish deficient for csf1r are viable and permit analyzing the consequences of macrophage loss throughout life.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc21012611
003      
CZ-PrNML
005      
20210507102032.0
007      
ta
008      
210420s2020 xxk f 000 0|eng||
009      
AR
024    7_
$a 10.7554/eLife.53403 $2 doi
035    __
$a (PubMed)32367800
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Kuil, Laura E $u Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, Netherlands
245    10
$a Zebrafish macrophage developmental arrest underlies depletion of microglia and reveals Csf1r-independent metaphocytes / $c LE. Kuil, N. Oosterhof, G. Ferrero, T. Mikulášová, M. Hason, J. Dekker, M. Rovira, HC. van der Linde, PM. van Strien, E. de Pater, G. Schaaf, EM. Bindels, V. Wittamer, TJ. van Ham
520    9_
$a Macrophages derive from multiple sources of hematopoietic progenitors. Most macrophages require colony-stimulating factor 1 receptor (CSF1R), but some macrophages persist in the absence of CSF1R. Here, we analyzed mpeg1:GFP-expressing macrophages in csf1r-deficient zebrafish and report that embryonic macrophages emerge followed by their developmental arrest. In larvae, mpeg1+ cell numbers then increased showing two distinct types in the skin: branched, putative Langerhans cells, and amoeboid cells. In contrast, although numbers also increased in csf1r-mutants, exclusively amoeboid mpeg1+ cells were present, which we showed by genetic lineage tracing to have a non-hematopoietic origin. They expressed macrophage-associated genes, but also showed decreased phagocytic gene expression and increased epithelial-associated gene expression, characteristic of metaphocytes, recently discovered ectoderm-derived cells. We further demonstrated that juvenile csf1r-deficient zebrafish exhibit systemic macrophage depletion. Thus, csf1r deficiency disrupts embryonic to adult macrophage development. Zebrafish deficient for csf1r are viable and permit analyzing the consequences of macrophage loss throughout life.
650    _2
$a zvířata $7 D000818
650    _2
$a proliferace buněk $7 D049109
650    _2
$a stanovení celkové genové exprese $7 D020869
650    _2
$a makrofágy $x metabolismus $x fyziologie $7 D008264
650    _2
$a mikroglie $x metabolismus $x fyziologie $7 D017628
650    _2
$a tyrosinkinasy $x metabolismus $7 D011505
650    _2
$a receptory faktoru stimulujícího granulocyto-makrofágové kolonie $x metabolismus $x fyziologie $7 D016187
650    _2
$a dánio pruhované $x embryologie $7 D015027
650    _2
$a proteiny dánia pruhovaného $x metabolismus $x fyziologie $7 D029961
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
655    _2
$a audiovizuální média $7 D059040
700    1_
$a Oosterhof, Nynke $u Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, Netherlands
700    1_
$a Ferrero, Giuliano $u Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire (IRIBHM), Université Libre de Bruxelles (ULB), Brussels, Belgium
700    1_
$a Mikulášová, Tereza $u Laboratory of Cell Differentiation, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic
700    1_
$a Hason, Martina $u Laboratory of Cell Differentiation, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic
700    1_
$a Dekker, Jordy $u Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, Netherlands
700    1_
$a Rovira, Mireia $u Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire (IRIBHM), Université Libre de Bruxelles (ULB), Brussels, Belgium
700    1_
$a van der Linde, Herma C $u Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, Netherlands
700    1_
$a van Strien, Paulina Mh $u Department of Hematology, Erasmus University Medical Center, Rotterdam, Netherlands
700    1_
$a de Pater, Emma $u Department of Hematology, Erasmus University Medical Center, Rotterdam, Netherlands
700    1_
$a Schaaf, Gerben $u Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, Netherlands
700    1_
$a Bindels, Erik Mj $u Department of Hematology, Erasmus University Medical Center, Rotterdam, Netherlands
700    1_
$a Wittamer, Valerie $u Institut de Recherche Interdisciplinaire en Biologie Humaine et Moléculaire (IRIBHM), Université Libre de Bruxelles (ULB), Brussels, Belgium $u WELBIO, ULB, Brussels, Belgium
700    1_
$a van Ham, Tjakko J $u Department of Clinical Genetics, Erasmus University Medical Center Rotterdam, Rotterdam, Netherlands
773    0_
$w MED00188753 $t eLife $x 2050-084X $g Roč. 9, č. - (2020)
856    41
$u https://pubmed.ncbi.nlm.nih.gov/32367800 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y p $z 0
990    __
$a 20210420 $b ABA008
991    __
$a 20210507102031 $b ABA008
999    __
$a ok $b bmc $g 1650887 $s 1132990
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 9 $c - $e 20200505 $i 2050-084X $m eLife $n eLife $x MED00188753
GRA    __
$a WELBIO-CR-2015S-04 $p WELBIO $2 International
GRA    __
$a 322368 $p Marie Curie $2 United Kingdom
GRA    __
$a VENI 016.136.150 $p ZonMw $2 Netherlands
GRA    __
$a F451218F $p Fonds de la Recherche Scientifique FNRS under Incentive Grant for Scientific Research $2 International
GRA    __
$a 18-18363S $p Czech Science Foundation $2 International
GRA    __
$a University Fellowship $p Erasmus University Rotterdam $2 International
GRA    __
$a 322368 $p Marie Curie Career Integration Grant $2 International
GRA    __
$a F451218F $p Fonds De La Recherche Scientifique - FNRS $2 International
LZP    __
$a Pubmed-20210420

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...