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Anderl, Ines
Publications (9 of 9) Show all publications
Schmid, M. R., Anderl, I., Vo, H. T. M., Valanne, S., Yang, H., Kronhamn, J., . . . Hultmark, D. (2016). Genetic Screen in Drosophila Larvae Links ird1 Function to Toll Signaling in the Fat Body and Hemocyte Motility. PLoS ONE, 11(7), Article ID e0159473.
Open this publication in new window or tab >>Genetic Screen in Drosophila Larvae Links ird1 Function to Toll Signaling in the Fat Body and Hemocyte Motility
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2016 (English)In: PLoS ONE, ISSN 1932-6203, E-ISSN 1932-6203, Vol. 11, no 7, article id e0159473Article in journal (Refereed) Published
Abstract [en]

To understand how Toll signaling controls the activation of a cellular immune response in Drosophila blood cells (hemocytes), we carried out a genetic modifier screen, looking for deletions that suppress or enhance the mobilization of sessile hemocytes by the gain-of-function mutation Toll(10b) (Tl-10b). Here we describe the results from chromosome arm 3R, where five regions strongly suppressed this phenotype. We identified the specific genes immune response deficient 1 (ird1), headcase (hdc) and possibly Rab23 as suppressors, and we studied the role of ird1 in more detail. An ird1 null mutant and a mutant that truncates the N-terminal kinase domain of the encoded Ird1 protein affected the Tl-10b phenotype, unlike mutations that affect the C-terminal part of the protein. The ird1 null mutant suppressed mobilization of sessile hemocytes, but enhanced other Tl-10b hemocyte phenotypes, like the formation of melanotic nodules and the increased number of circulating hemocytes. ird1 mutants also had blood cell phenotypes on their own. They lacked crystal cells and showed aberrant formation of lamellocytes. ird1 mutant plasmatocytes had a reduced ability to spread on an artificial substrate by forming protrusions, which may explain why they did not go into circulation in response to Toll signaling. The effect of the ird1 mutation depended mainly on ird1 expression in hemocytes, but ird1-dependent effects in other tissues may contribute. Specifically, the Toll receptor was translocated from the cell membrane to intracellular vesicles in the fat body of the ird1 mutant, and Toll signaling was activated in that tissue, partially explaining the Tl-10b-like phenotype. As ird1 is otherwise known to control vesicular transport, we conclude that the vesicular transport system may be of particular importance during an immune response.

National Category
Cell and Molecular Biology
Identifiers
urn:nbn:se:umu:diva-126336 (URN)10.1371/journal.pone.0159473 (DOI)000381516100034 ()27467079 (PubMedID)
Available from: 2016-10-25 Created: 2016-10-03 Last updated: 2018-06-09Bibliographically approved
Anderl, I., Vesala, L., Ihalainen, T. O., Vanha-aho, L.-M., Andó, I., Rämet, M. & Hultmark, D. (2016). Transdifferentiation and Proliferation in Two Distinct Hemocyte Lineages in Drosophila melanogaster Larvae after Wasp Infection. PLoS Pathogens, 12(7), Article ID e1005746.
Open this publication in new window or tab >>Transdifferentiation and Proliferation in Two Distinct Hemocyte Lineages in Drosophila melanogaster Larvae after Wasp Infection
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2016 (English)In: PLoS Pathogens, ISSN 1553-7366, E-ISSN 1553-7374, Vol. 12, no 7, article id e1005746Article in journal (Refereed) Published
Abstract [en]

Cellular immune responses require the generation and recruitment of diverse blood cell types that recognize and kill pathogens. In Drosophila melanogaster larvae, immune-inducible lamellocytes participate in recognizing and killing parasitoid wasp eggs. However, the sequence of events required for lamellocyte generation remains controversial. To study the cellular immune system, we developed a flow cytometry approach using in vivo reporters for lamellocytes as well as for plasmatocytes, the main hemocyte type in healthy larvae. We found that two different blood cell lineages, the plasmatocyte and lamellocyte lineages, contribute to the generation of lamellocytes in a demand-adapted hematopoietic process. Plasmatocytes transdifferentiate into lamellocyte-like cells in situ directly on the wasp egg. In parallel, a novel population of infection-induced cells, which we named lamelloblasts, appears in the circulation. Lamelloblasts proliferate vigorously and develop into the major class of circulating lamellocytes. Our data indicate that lamellocyte differentiation upon wasp parasitism is a plastic and dynamic process. Flow cytometry with in vivo hemocyte reporters can be used to study this phenomenon in detail.

Place, publisher, year, edition, pages
Public library science, 2016
National Category
Microbiology in the medical area Immunology in the medical area
Identifiers
urn:nbn:se:umu:diva-126760 (URN)10.1371/journal.ppat.1005746 (DOI)000383366400030 ()
Available from: 2016-10-18 Created: 2016-10-13 Last updated: 2018-06-09Bibliographically approved
Anderl, I. (2015). Activation of the Cellular Immune Response in Drosophila melanogaster Larvae. (Doctoral dissertation). Umeå: Umeå University
Open this publication in new window or tab >>Activation of the Cellular Immune Response in Drosophila melanogaster Larvae
2015 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

During the last 40 years, Drosophila melanogaster has become an invaluable tool in understanding innate immunity. The innate immune system of Drosophila consists of a humoral and a cellular component. While many details are known about the humoral immune system, our knowledge about the cellular immune system is comparatively small. Blood cells or hemocytes constitute the cellular immune system. Three blood types have been described for Drosophila larvae. Plasmatocytes are phagocytes with a plethora of functions. Crystal cells mediate melanization and contribute to wound healing. Plasmatocytes and crystal cells constitute the blood cell repertoire of a healthy larva, whereas lamellocytes are induced in a demand-adapted manner after infection with parasitoid wasp eggs. They are involved in the melanotic encapsulation response against parasites and form melanotic nodules that are also referred to as tumors.

In my thesis, I focused on unraveling the mechanisms of how the immune system orchestrates the cellular immune response. In particular, I was interested in the hematopoiesis of lamellocytes.

In Article I, we were able to show that ectopic expression of key components of a number of signaling pathways in blood cells induced the development of lamellocytes, led to a proliferative response of plasmatocytes, or to a combination of lamellocyte activation and plasmatocyte proliferation.

In Article II, I combined newly developed fluorescent enhancer-reporter constructs specific for plasmatocytes and lamellocytes and developed a “dual reporter system” that was used in live microscopy of fly larvae. In addition, we established flow cytometry as a tool to count total blood cell numbers and to distinguish between different blood cell types. The “dual reporter system” enabled us to differentiate between six blood cell types and established proliferation as a central feature of the cellular immune response. The combination flow cytometry and live imaging increased our understanding of the tempo-spatial events leading to the cellular immune reaction.

In Article III, I developed a genetic modifier screen to find genes involved in the hematopoiesis of lamellocytes. I took advantage of the gain-of-function phenotype of the Tl10b mutation characterized by an activated cellular immune system, which induced the formation blood cell tumors. We screened the right arm of chromosome 3 for enhancers and suppressors of this mutation and uncovered ird1.

Finally in Article IV, we showed that the activity of the Toll signaling pathway in the fat body, the homolog of the liver, is necessary to activate the cellular immune system and induce lamellocyte hematopoiesis.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2015. p. 41
Series
Umeå University medical dissertations, ISSN 0346-6612 ; 1741
Keywords
Drosophila melanogaster, immunity, blood cells, hematopoiesis, flow cytometry, in vivo imaging, genetic screens, Tl10b, fat body, Toll signaling
National Category
Immunology
Research subject
Molecular Biology
Identifiers
urn:nbn:se:umu:diva-106981 (URN)978-91-7601-317-5 (ISBN)
Public defence
2015-09-07, Major Groove, Byggnad 6L, Umeå, 12:30 (English)
Opponent
Supervisors
Available from: 2015-08-17 Created: 2015-08-13 Last updated: 2018-06-07Bibliographically approved
Vanha-aho, L.-M., Anderl, I., Vesala, L., Hultmark, D., Valanne, S. & Rämet, M. (2015). Edin expression in the fat body is required in the defense against parasitic wasps in Drosophila melanogaster. PLoS Pathogens, 11(5), Article ID e1004895.
Open this publication in new window or tab >>Edin expression in the fat body is required in the defense against parasitic wasps in Drosophila melanogaster
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2015 (English)In: PLoS Pathogens, ISSN 1553-7366, E-ISSN 1553-7374, Vol. 11, no 5, article id e1004895Article in journal (Refereed) Published
Abstract [en]

The cellular immune response against parasitoid wasps in Drosophila involves the activation, mobilization, proliferation and differentiation of different blood cell types. Here, we have assessed the role of Edin (elevated during infection) in the immune response against the parasitoid wasp Leptopilina boulardi in Drosophila melanogaster larvae. The expression of edin was induced within hours after a wasp infection in larval fat bodies. Using tissue-specific RNAi, we show that Edin is an important determinant of the encapsulation response. Although edin expression in the fat body was required for the larvae to mount a normal encapsulation response, it was dispensable in hemocytes. Edin expression in the fat body was not required for lamellocyte differentiation, but it was needed for the increase in plasmatocyte numbers and for the release of sessile hemocytes into the hemolymph. We conclude that edin expression in the fat body affects the outcome of a wasp infection by regulating the increase of plasmatocyte numbers and the mobilization of sessile hemocytes in Drosophila larvae.

Place, publisher, year, edition, pages
Public library science, 2015
National Category
Infectious Medicine Microbiology in the medical area
Identifiers
urn:nbn:se:umu:diva-105266 (URN)10.1371/journal.ppat.1004895 (DOI)000355269300039 ()25965263 (PubMedID)
Available from: 2015-06-22 Created: 2015-06-22 Last updated: 2018-06-07Bibliographically approved
Anderl, I. & Hultmark, D. (2015). New ways to make a blood cell. eLIFE, 4, Article ID e06877.
Open this publication in new window or tab >>New ways to make a blood cell
2015 (English)In: eLIFE, E-ISSN 2050-084X, Vol. 4, article id e06877Article in journal, Editorial material (Other academic) Published
National Category
Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)
Identifiers
urn:nbn:se:umu:diva-102220 (URN)10.7554/eLife.06877 (DOI)000351865000003 ()
Available from: 2015-05-10 Created: 2015-04-22 Last updated: 2018-06-07Bibliographically approved
Schmid, M. R., Anderl, I., Vesala, L., Vanha-aho, L.-M., Deng, X.-J., Rämet, M. & Hultmark, D. (2014). Control of Drosophila blood cell activation via toll signaling in the fat body. PLoS ONE, 9(8), Article ID e102568.
Open this publication in new window or tab >>Control of Drosophila blood cell activation via toll signaling in the fat body
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2014 (English)In: PLoS ONE, ISSN 1932-6203, E-ISSN 1932-6203, Vol. 9, no 8, article id e102568Article in journal (Refereed) Published
Abstract [en]

The Toll signaling pathway, first discovered in Drosophila, has a well-established role in immune responses in insects as well as in mammals. In Drosophila, the Toll-dependent induction of antimicrobial peptide production has been intensely studied as a model for innate immune responses in general. Besides this humoral immune response, Toll signaling is also known to activate blood cells in a reaction that is similar to the cellular immune response to parasite infections, but the mechanisms of this response are poorly understood. Here we have studied this response in detail, and found that Toll signaling in several different tissues can activate a cellular immune defense, and that this response does not require Toll signaling in the blood cells themselves. Like in the humoral immune response, we show that Toll signaling in the fat body (analogous to the liver in vertebrates) is of major importance in the Toll-dependent activation of blood cells. However, this Toll-dependent mechanism of blood cell activation contributes very little to the immune response against the parasitoid wasp, Leptopilina boulardi, probably because the wasp is able to suppress Toll induction. Other redundant pathways may be more important in the defense against this pathogen.

Place, publisher, year, edition, pages
Public library of science, 2014
Keywords
Drosophila, toll signaling, immunity, hemocytes, fat body
National Category
Cell and Molecular Biology Microbiology
Research subject
Molecular Biology; biology
Identifiers
urn:nbn:se:umu:diva-92747 (URN)10.1371/journal.pone.0102568 (DOI)000339993900003 ()25102059 (PubMedID)
Funder
Swedish Research Council
Available from: 2014-09-02 Created: 2014-09-02 Last updated: 2018-06-07Bibliographically approved
Zettervall, C.-J., Anderl, I., Williams, M., Palmer, R., Kurucz, E., Ando, I. & Hultmark, D. (2004). A directed screen for genes involved in Drosophila blood cell activation. Proceedings of the National Academy of Sciences of the United States of America, 101(39), 14192-14197
Open this publication in new window or tab >>A directed screen for genes involved in Drosophila blood cell activation
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2004 (English)In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 101, no 39, p. 14192-14197Article in journal (Refereed) Published
Abstract [en]

An attack by a parasitic wasp activates a vigorous cellular immune response in Drosophila larvae. This response is manifested by an increased number of circulating cells, the hemocytes, and by the appearance of a specialized class of hemocyte, the lamellocytes, which participate in the encapsulation and killing of the parasite. To study the molecular mechanisms of this response, we have overexpressed different genes in the hemocytes, by using the GAL4-upstream activating sequence system and a hemocyte-specific Hemese-GAL4 driver. Multiple transgenes were tested, representing several important signaling pathways. We found that the proliferation response and the activation of lamellocyte formation are independent phenomena. A drastic increase in the number of circulating hemocytes is caused by receptor tyrosine kinases, such as Egfr, Pvr, and Alk, as well as by the downstream signaling components Ras85D and pointed, supporting the notion that the Ras-mitogen-activated protein kinase pathway regulates hemocyte numbers. In the case of Pvr and Alk, this phenotype also is accompanied by lamellocyte formation. By contrast, constitutively active hopscotch and hemipterous give massive activation of lamellocyte formation with little or no increase in total hemocyte numbers. This finding indicates that both the Jak/Stat and the Jun kinase pathways affect lamellocyte formation. Still other signals, mediated by aop(ACT), Toll(10b), and Rac1 expression, cause a simultaneous increase in lamellocyte and total cell numbers, and the same effect is seen when WNT signaling is suppressed. We conclude that the activation of a cellular response is complex and affected by multiple signaling pathways.

Place, publisher, year, edition, pages
Washington: National Academy of Sciences, 2004
Keywords
Animals, Drosophila/*genetics/*immunology/parasitology, Drosophila Proteins/genetics/metabolism, Female, Gene Expression, Hemocytes/enzymology/immunology/parasitology/*physiology, Larva/immunology/metabolism/parasitology, Male, Phenotype, Receptor Protein-Tyrosine Kinases/metabolism, Recombinant Fusion Proteins/genetics/metabolism, Signal Transduction, Transgenes/*genetics, Wasps/immunology, beta-Galactosidase/genetics, ras Proteins/metabolism
National Category
Infectious Medicine
Identifiers
urn:nbn:se:umu:diva-17054 (URN)10.1073/pnas.0403789101 (DOI)000224211400042 ()15381778 (PubMedID)
Available from: 2007-10-28 Created: 2007-10-28 Last updated: 2018-06-09Bibliographically approved
Schmid, M. R., Anderl, I., Valanne, S., Vo, H., Yang, H., Kronhamn, J., . . . Hultmark, D.Genetic screen in Drosophila larvae links ird1 function to Toll signaling in the fat body and hemocyte motility.
Open this publication in new window or tab >>Genetic screen in Drosophila larvae links ird1 function to Toll signaling in the fat body and hemocyte motility
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(English)Manuscript (preprint) (Other academic)
National Category
Microbiology
Identifiers
urn:nbn:se:umu:diva-92811 (URN)
Available from: 2014-09-04 Created: 2014-09-04 Last updated: 2018-06-07Bibliographically approved
Anderl, I.Infection-induced proliferation is a central hallmark of the activation of the cellular immune response in Drosophila larvae..
Open this publication in new window or tab >>Infection-induced proliferation is a central hallmark of the activation of the cellular immune response in Drosophila larvae.
(English)Manuscript (preprint) (Other academic)
Abstract [en]

Blood cells have important roles in immune reactions in all metazoan species. In Drosophila melanogaster larvae, phagocytic plasmatocytes are the main blood cell (hemocyte) type. Lamellocytes participate in encapsulating foreign objects and are formed in response to parasitoid wasps laying their eggs into the hemocoel of the larvae. The immune reaction against wasps requires controlled recruitment and action of hemocytes from the lymph glands, sessile islets and circulation. However, the contribution of these different hematopoietic compartments to the immune-induced hemocyte pool remains unclear. We used eater-GFP and MSNF9MO-mCherry to fluorescently tag plasmatocytes and lamellocytes, respectively, and utilized flow cytometry and in vivo imaging to assess the hemocyte numbers and types in circulation and in sessile compartments after infection by three wasp species of the genus Leptopilina. We detected five different hemocyte types based on fluorescence, and a population of non-fluorescent cells. While non-infected larvae generally had only one, eaterGFP-high plasmatocyte population, early after wasp infection a new, eaterGFP-low cell population appeared in circulation. EaterGFP-high and –low cells both accumulated msnCherry during the immune response, and formed two cell lineages. Whereas the eaterGFP-low cells gradually lost GFP, the eaterGFP-high cells retained it at high levels. We suggest that eaterGFP-low cells represent an immune-induced hemocyte precursor cell pool, which, via a prelamellocyte stage, gives rise to lamellocytes. EaterGFP-high plasmatocytes also differentiated into large, msnCherry-positive hemocytes on wasp eggs, but these cells retain plasmatocyte identity. Importantly, all hemocyte types, except for lamellocytes, were able to divide after wasp infection, contributing to the increased hemocyte numbers after infection. We conclude that orchestrated differentiation and division of different hemocyte types in circulation and in sessile compartment is key to a successful immune response against parasitoid wasps.

National Category
Immunology
Research subject
Molecular Biology
Identifiers
urn:nbn:se:umu:diva-106978 (URN)
Available from: 2015-08-13 Created: 2015-08-13 Last updated: 2018-06-07Bibliographically approved
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