Supplementary MaterialsData Document S1: Data Document S1

Supplementary MaterialsData Document S1: Data Document S1. = Gr1) at a macrolesion (gray). See Amount 1A. B) Pre-recruited leading get in touch with neutrophils (magenta = Gr1) go through cell loss of life upon connection with tissues debris (greyish) and initiate following swarming behavior. Find Amount 1B. C) Leading neutrophil (magenta = LysM) undergoes cell death upon connection with individual bacterium (white = Salmonella) and initiates subsequent swarming behavior. Observe Number S1I. D) Intravital visualization of pre-recruited neutrophil (magenta = Gr1) swarming at a macrolesion, and the HOE 32021 consequent changes in injury size (gray = autofluorescence) and collagen disruption/displacement (orange = second harmonics). Observe Number 1D. E) Visualization of the death of a pre-recruited contact neutrophil (magenta = Gr1) at a laser-induced microlesion (gray). See Number S2G. F) Swarming of pre-recruited neutrophils (magenta = LysM) at a macrolesion (gray; top) or a microlesion (gray; bottom). See Number 1E. G) Intravital visualization of pre-recruited neutrophil (magenta = Gr1) swarming at a microlesion, and the consequent changes in injury size (gray = autofluorescence) and collagen disruption/displacement (orange = second harmonics). Observe Number 1F. H) Swarming dynamics of endogenously recruited neutrophils (magenta = LysM) at a macrolesion (gray). See Number 1G. I) Assessment of representative IVM-derived tracking data of pre-recruited (remaining) and endogenously recruited (right) neutrophils at a microlesion, respectively. Video starts as soon as neutrophils enter the imaging field. See Number 1HC1I. NIHMS1017759-supplement-Movie_S2.mp4 (107M) GUID:?D366844B-897D-42D8-B4F3-2030C7ADC517 Movie S3: Movie S3. RTM cloak cells microlesions, Related to Number 2. A) Intravital imaging of the peritoneal serosa showing a human population HOE 32021 of nonmigratory resident cells macrophages (green = LysM), and few mobile cells, likely migratory monocytes. Observe Number 2A.B) Intravital visualization HOE 32021 of the resting sampling activity of an individual RTM (green = LysM), and its dynamic response to a sterile cells injury (bottom; not visible). See Number 2B. C) Cloaking dynamics of RTM (green = LysM) responding to a laser-induced microlesion (orange), as well as IVM-derived tracking data of individual pseudopods originating from macrophages in the larger sensing zone (cyan) and closer convergence zone (yellow). See Number 2C. NIHMS1017759-supplement-Movie_S3.mp4 (59M) GUID:?07170988-F944-47FD-A307-AD1765FCD13E Movie S4: Movie S4. Cloaking by RTM prevents neutrophil swarming, Related to Number 3. A) Dynamics of neutrophils endogenously recruited to microlesions in the presence or absence of cloaking RTM (green = LysM) in CD169-DTR mice treated with vehicle (top) or DT (bottom). Sequences start as soon as neutrophils (magenta = Gr1) enter the imaging field. Observe Number 3B.B) Cloaking by RTM (green = LysM) and endogenous neutrophil response (magenta = LysM-high) at two sequential microlesions close to each other. Lesion 1 was induced 20 moments before movie starts. See Number 3E. NIHMS1017759-supplement-Movie_S4.mp4 (67M) GUID:?6DC359D8-CF9D-4757-B983-18DA4EDE98F0 Movie S5: HOE 32021 Movie S5. Secondary damage containment by FSCN1 monocytes, Related to Number 5 and Number S4. A) Dynamic behavior of migratory monocytes (yellow = CCR2) under resting conditions and in response to laser-induced tissue damage. See Number S4F.B) Intravital visualization of the dynamic response of migratory CX3CR1+ (blue) or CCR2+ (yellow) monocytes to a macro-lesion in monocyte reporter mice (bacteria (white colored) topically applied on the peritoneal serosa. Cyan outlines = Neutrophil swarms. Sequence HOE 32021 representative of 3 self-employed experiments. Scale pub, 100 m. Observe Film S2A. F) Consultant (n 5) IVM-sequence displaying a respected neutrophil (magenta = Gr1) going through terminal activation upon connection with tissues debris (greyish = autofluorescence)..