Mitochondria Transfer in Bone Marrow Hematopoietic Activity
Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication medi...
Ausführliche Beschreibung
Autor*in: |
Singh, Abhishek K. [verfasserIn] Cancelas, Jose A. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Current stem cell reports - Berlin [u.a.] : Springer, 2015, 7(2021), 1 vom: 04. Jan., Seite 1-12 |
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Übergeordnetes Werk: |
volume:7 ; year:2021 ; number:1 ; day:04 ; month:01 ; pages:1-12 |
Links: |
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DOI / URN: |
10.1007/s40778-020-00185-z |
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Katalog-ID: |
SPR043523242 |
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100 | 1 | |a Singh, Abhishek K. |e verfasserin |4 aut | |
245 | 1 | 0 | |a Mitochondria Transfer in Bone Marrow Hematopoietic Activity |
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520 | |a Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. | ||
650 | 4 | |a Hematopoietic stem cells |7 (dpeaa)DE-He213 | |
650 | 4 | |a Mesenchymal stromal cells |7 (dpeaa)DE-He213 | |
650 | 4 | |a Mitochondrial dynamics and transfer |7 (dpeaa)DE-He213 | |
650 | 4 | |a Reactive oxygen species |7 (dpeaa)DE-He213 | |
650 | 4 | |a Gap junction |7 (dpeaa)DE-He213 | |
650 | 4 | |a Tunneling nanotubes |7 (dpeaa)DE-He213 | |
700 | 1 | |a Cancelas, Jose A. |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Current stem cell reports |d Berlin [u.a.] : Springer, 2015 |g 7(2021), 1 vom: 04. Jan., Seite 1-12 |w (DE-627)817361081 |w (DE-600)2808623-5 |x 2198-7866 |7 nnns |
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allfields |
10.1007/s40778-020-00185-z doi (DE-627)SPR043523242 (DE-599)SPRs40778-020-00185-z-e (SPR)s40778-020-00185-z-e DE-627 ger DE-627 rakwb eng 610 ASE Singh, Abhishek K. verfasserin aut Mitochondria Transfer in Bone Marrow Hematopoietic Activity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. Hematopoietic stem cells (dpeaa)DE-He213 Mesenchymal stromal cells (dpeaa)DE-He213 Mitochondrial dynamics and transfer (dpeaa)DE-He213 Reactive oxygen species (dpeaa)DE-He213 Gap junction (dpeaa)DE-He213 Tunneling nanotubes (dpeaa)DE-He213 Cancelas, Jose A. verfasserin aut Enthalten in Current stem cell reports Berlin [u.a.] : Springer, 2015 7(2021), 1 vom: 04. Jan., Seite 1-12 (DE-627)817361081 (DE-600)2808623-5 2198-7866 nnns volume:7 year:2021 number:1 day:04 month:01 pages:1-12 https://dx.doi.org/10.1007/s40778-020-00185-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2021 1 04 01 1-12 |
spelling |
10.1007/s40778-020-00185-z doi (DE-627)SPR043523242 (DE-599)SPRs40778-020-00185-z-e (SPR)s40778-020-00185-z-e DE-627 ger DE-627 rakwb eng 610 ASE Singh, Abhishek K. verfasserin aut Mitochondria Transfer in Bone Marrow Hematopoietic Activity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. Hematopoietic stem cells (dpeaa)DE-He213 Mesenchymal stromal cells (dpeaa)DE-He213 Mitochondrial dynamics and transfer (dpeaa)DE-He213 Reactive oxygen species (dpeaa)DE-He213 Gap junction (dpeaa)DE-He213 Tunneling nanotubes (dpeaa)DE-He213 Cancelas, Jose A. verfasserin aut Enthalten in Current stem cell reports Berlin [u.a.] : Springer, 2015 7(2021), 1 vom: 04. Jan., Seite 1-12 (DE-627)817361081 (DE-600)2808623-5 2198-7866 nnns volume:7 year:2021 number:1 day:04 month:01 pages:1-12 https://dx.doi.org/10.1007/s40778-020-00185-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2021 1 04 01 1-12 |
allfields_unstemmed |
10.1007/s40778-020-00185-z doi (DE-627)SPR043523242 (DE-599)SPRs40778-020-00185-z-e (SPR)s40778-020-00185-z-e DE-627 ger DE-627 rakwb eng 610 ASE Singh, Abhishek K. verfasserin aut Mitochondria Transfer in Bone Marrow Hematopoietic Activity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. Hematopoietic stem cells (dpeaa)DE-He213 Mesenchymal stromal cells (dpeaa)DE-He213 Mitochondrial dynamics and transfer (dpeaa)DE-He213 Reactive oxygen species (dpeaa)DE-He213 Gap junction (dpeaa)DE-He213 Tunneling nanotubes (dpeaa)DE-He213 Cancelas, Jose A. verfasserin aut Enthalten in Current stem cell reports Berlin [u.a.] : Springer, 2015 7(2021), 1 vom: 04. Jan., Seite 1-12 (DE-627)817361081 (DE-600)2808623-5 2198-7866 nnns volume:7 year:2021 number:1 day:04 month:01 pages:1-12 https://dx.doi.org/10.1007/s40778-020-00185-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2021 1 04 01 1-12 |
allfieldsGer |
10.1007/s40778-020-00185-z doi (DE-627)SPR043523242 (DE-599)SPRs40778-020-00185-z-e (SPR)s40778-020-00185-z-e DE-627 ger DE-627 rakwb eng 610 ASE Singh, Abhishek K. verfasserin aut Mitochondria Transfer in Bone Marrow Hematopoietic Activity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. Hematopoietic stem cells (dpeaa)DE-He213 Mesenchymal stromal cells (dpeaa)DE-He213 Mitochondrial dynamics and transfer (dpeaa)DE-He213 Reactive oxygen species (dpeaa)DE-He213 Gap junction (dpeaa)DE-He213 Tunneling nanotubes (dpeaa)DE-He213 Cancelas, Jose A. verfasserin aut Enthalten in Current stem cell reports Berlin [u.a.] : Springer, 2015 7(2021), 1 vom: 04. Jan., Seite 1-12 (DE-627)817361081 (DE-600)2808623-5 2198-7866 nnns volume:7 year:2021 number:1 day:04 month:01 pages:1-12 https://dx.doi.org/10.1007/s40778-020-00185-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2021 1 04 01 1-12 |
allfieldsSound |
10.1007/s40778-020-00185-z doi (DE-627)SPR043523242 (DE-599)SPRs40778-020-00185-z-e (SPR)s40778-020-00185-z-e DE-627 ger DE-627 rakwb eng 610 ASE Singh, Abhishek K. verfasserin aut Mitochondria Transfer in Bone Marrow Hematopoietic Activity 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. Hematopoietic stem cells (dpeaa)DE-He213 Mesenchymal stromal cells (dpeaa)DE-He213 Mitochondrial dynamics and transfer (dpeaa)DE-He213 Reactive oxygen species (dpeaa)DE-He213 Gap junction (dpeaa)DE-He213 Tunneling nanotubes (dpeaa)DE-He213 Cancelas, Jose A. verfasserin aut Enthalten in Current stem cell reports Berlin [u.a.] : Springer, 2015 7(2021), 1 vom: 04. Jan., Seite 1-12 (DE-627)817361081 (DE-600)2808623-5 2198-7866 nnns volume:7 year:2021 number:1 day:04 month:01 pages:1-12 https://dx.doi.org/10.1007/s40778-020-00185-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 7 2021 1 04 01 1-12 |
language |
English |
source |
Enthalten in Current stem cell reports 7(2021), 1 vom: 04. Jan., Seite 1-12 volume:7 year:2021 number:1 day:04 month:01 pages:1-12 |
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Enthalten in Current stem cell reports 7(2021), 1 vom: 04. Jan., Seite 1-12 volume:7 year:2021 number:1 day:04 month:01 pages:1-12 |
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Hematopoietic stem cells Mesenchymal stromal cells Mitochondrial dynamics and transfer Reactive oxygen species Gap junction Tunneling nanotubes |
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Singh, Abhishek K. @@aut@@ Cancelas, Jose A. @@aut@@ |
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Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. 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Singh, Abhishek K. |
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Singh, Abhishek K. ddc 610 misc Hematopoietic stem cells misc Mesenchymal stromal cells misc Mitochondrial dynamics and transfer misc Reactive oxygen species misc Gap junction misc Tunneling nanotubes Mitochondria Transfer in Bone Marrow Hematopoietic Activity |
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610 ASE Mitochondria Transfer in Bone Marrow Hematopoietic Activity Hematopoietic stem cells (dpeaa)DE-He213 Mesenchymal stromal cells (dpeaa)DE-He213 Mitochondrial dynamics and transfer (dpeaa)DE-He213 Reactive oxygen species (dpeaa)DE-He213 Gap junction (dpeaa)DE-He213 Tunneling nanotubes (dpeaa)DE-He213 |
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ddc 610 misc Hematopoietic stem cells misc Mesenchymal stromal cells misc Mitochondrial dynamics and transfer misc Reactive oxygen species misc Gap junction misc Tunneling nanotubes |
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Mitochondria Transfer in Bone Marrow Hematopoietic Activity |
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Mitochondria Transfer in Bone Marrow Hematopoietic Activity |
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mitochondria transfer in bone marrow hematopoietic activity |
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Mitochondria Transfer in Bone Marrow Hematopoietic Activity |
abstract |
Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. |
abstractGer |
Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. |
abstract_unstemmed |
Purpose of Review The well-established crosstalk between hematopoietic stem cells (HSC) and bone marrow (BM) microenvironment is critical for the homeostasis and hematopoietic regeneration in response to blood formation emergencies. Past decade has witnessed that the intercellular communication mediated by the transfer of cytoplasmic material and organelles between cells can regenerate and/or repair the damaged cells. Mitochondria have recently emerged as a potential regulator of HSC fate. This review intends to discuss recent advances in the understanding of the mitochondrial dynamics, specifically focused on the role of mitochondrial transfer, in the maintenance of HSC activity with clear implications in stem cell transplantation and regenerative medicine. Recent Findings HSC are highly heterogeneous in their mitochondrial metabolism, and the quiescence and potency of HSC depend on the status of mitochondrial dynamics and the clearance of damaged mitochondria. Recent evidence has shown that in stress response, BM stromal cells transfer healthy mitochondria to HSC, facilitate HSC bioenergetics shift towards oxidative phosphorylation, and subsequently stimulate leukocyte expansion. Furthermore, metabolic rewiring following mitochondria transfer from HSPC to BM stromal cells likely to repair the damaged BM niche and accelerate limiting HSC transplantation post myeloablative conditioning. Summary The alteration of mitochondrial dynamics, damaged mitochondrial clearance, and intercellular mitochondria transfer, fine-tuned by BM niche factors and stress signaling, has considerable impacts on hematopoietic and BM microenvironment regeneration. Elucidating the differential BM niche component on mitochondria transfer, the trigger signal, mode of transfer, and the fate of transferred mitochondria are essential to underpin their application in regenerative medicine and transplantation settings. |
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title_short |
Mitochondria Transfer in Bone Marrow Hematopoietic Activity |
url |
https://dx.doi.org/10.1007/s40778-020-00185-z |
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Cancelas, Jose A. |
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Cancelas, Jose A. |
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10.1007/s40778-020-00185-z |
up_date |
2024-07-03T19:13:01.707Z |
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score |
7.400508 |