Site-1 protease ablation in the osterix-lineage in mice results in bone marrow neutrophilia and hematopoietic stem cell alterations
© 2020. Published by The Company of Biologists Ltd..
Site-1 protease (S1P) ablation in the osterix-lineage in mice drastically reduces bone development and downregulates bone marrow-derived skeletal stem cells. Here we show that these mice also suffer from spina bifida occulta with a characteristic lack of bone fusion in the posterior neural arches. Molecular analysis of bone marrow-derived non-red blood cell cells, via single-cell RNA-Seq and protein mass spectrometry, demonstrate that these mice have a much-altered bone marrow with a significant increase in neutrophils and Ly6C-expressing leukocytes. The molecular composition of bone marrow neutrophils is also different as they express more and additional members of the stefin A (Stfa) family of proteins. In vitro, recombinant Stfa1 and Stfa2 proteins have the ability to drastically inhibit osteogenic differentiation of bone marrow stromal cells, with no effect on adipogenic differentiation. FACS analysis of hematopoietic stem cells show that despite a decrease in hematopoietic stem cells, S1P ablation results in an increased production of granulocyte-macrophage progenitors, the precursors to neutrophils. These observations indicate that S1P has a role in the lineage specification of hematopoietic stem cells and/or their progenitors for development of a normal hematopoietic niche. Our study designates a fundamental requirement of S1P for maintaining a balanced regenerative capacity of the bone marrow niche.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:9 |
---|---|
Enthalten in: |
Biology open - 9(2020), 6 vom: 23. Juni |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Patra, Debabrata [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 24.08.2021 Date Revised 27.04.2024 published: Electronic Citation Status MEDLINE |
---|
doi: |
10.1242/bio.052993 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM31155041X |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM31155041X | ||
003 | DE-627 | ||
005 | 20240427231847.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2020 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1242/bio.052993 |2 doi | |
028 | 5 | 2 | |a pubmed24n1390.xml |
035 | |a (DE-627)NLM31155041X | ||
035 | |a (NLM)32576566 | ||
035 | |a (PII)bio052993 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Patra, Debabrata |e verfasserin |4 aut | |
245 | 1 | 0 | |a Site-1 protease ablation in the osterix-lineage in mice results in bone marrow neutrophilia and hematopoietic stem cell alterations |
264 | 1 | |c 2020 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 24.08.2021 | ||
500 | |a Date Revised 27.04.2024 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2020. Published by The Company of Biologists Ltd. | ||
520 | |a Site-1 protease (S1P) ablation in the osterix-lineage in mice drastically reduces bone development and downregulates bone marrow-derived skeletal stem cells. Here we show that these mice also suffer from spina bifida occulta with a characteristic lack of bone fusion in the posterior neural arches. Molecular analysis of bone marrow-derived non-red blood cell cells, via single-cell RNA-Seq and protein mass spectrometry, demonstrate that these mice have a much-altered bone marrow with a significant increase in neutrophils and Ly6C-expressing leukocytes. The molecular composition of bone marrow neutrophils is also different as they express more and additional members of the stefin A (Stfa) family of proteins. In vitro, recombinant Stfa1 and Stfa2 proteins have the ability to drastically inhibit osteogenic differentiation of bone marrow stromal cells, with no effect on adipogenic differentiation. FACS analysis of hematopoietic stem cells show that despite a decrease in hematopoietic stem cells, S1P ablation results in an increased production of granulocyte-macrophage progenitors, the precursors to neutrophils. These observations indicate that S1P has a role in the lineage specification of hematopoietic stem cells and/or their progenitors for development of a normal hematopoietic niche. Our study designates a fundamental requirement of S1P for maintaining a balanced regenerative capacity of the bone marrow niche | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Hematopoietic stem cells | |
650 | 4 | |a Neutrophilia | |
650 | 4 | |a Osteopenia | |
650 | 4 | |a Osterix | |
650 | 4 | |a Site-1 protease | |
650 | 4 | |a Stefin | |
650 | 7 | |a Sp7 Transcription Factor |2 NLM | |
650 | 7 | |a Sp7 protein, mouse |2 NLM | |
650 | 7 | |a Proprotein Convertases |2 NLM | |
650 | 7 | |a EC 3.4.21.- |2 NLM | |
650 | 7 | |a Serine Endopeptidases |2 NLM | |
650 | 7 | |a EC 3.4.21.- |2 NLM | |
650 | 7 | |a membrane-bound transcription factor peptidase, site 1 |2 NLM | |
650 | 7 | |a EC 3.4.21.112 |2 NLM | |
700 | 1 | |a Kim, Joongho |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Qiang |e verfasserin |4 aut | |
700 | 1 | |a Tycksen, Eric |e verfasserin |4 aut | |
700 | 1 | |a Sandell, Linda J |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Biology open |d 2012 |g 9(2020), 6 vom: 23. Juni |w (DE-627)NLM222372419 |x 2046-6390 |7 nnns |
773 | 1 | 8 | |g volume:9 |g year:2020 |g number:6 |g day:23 |g month:06 |
856 | 4 | 0 | |u http://dx.doi.org/10.1242/bio.052993 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 9 |j 2020 |e 6 |b 23 |c 06 |