HIF-2α is essential for carotid body development and function

  1. David Macias  Is a corresponding author
  2. Andrew S Cowburn
  3. Hortensia Torres-Torrelo
  4. Patricia Ortega-Sáenz
  5. José López-Barneo
  6. Randall S Johnson  Is a corresponding author
  1. University of Cambridge, United Kingdom
  2. Instituto de Biomedicina de Sevilla, Spain
  3. Karolinska Institute, Sweden
10 figures, 1 table and 1 additional file

Figures

Figure 1 with 1 supplement
Selective loss of carotid body glomus cells in sympathoadrenal-specific Epas1, but not Hif1a, deficient mice.

(A and B) Tyrosine hydroxylase (TH) immunostaining on carotid bifurcation sections from HIF-2αWT (A, top panels), TH-HIF-2αKO (A, bottom panels), HIF-1αWT (B, top panels) and TH-HIF-1αKO (B, bottom panels) mice (8–12 weeks old). Micrographs showed in A (bottom) were selected to illustrate the rare presence of TH+ glomus cells in TH-HIF-2αKO mice (white arrowheads). Dashed rectangles (left panels) are shown at higher magnification on the right panels. SCG, superior cervical ganglion; CB, carotid body; ICA, internal carotid artery; ECA, external carotid artery. Scale bars: 200 µm (left panels), 50 µm (right panels). (C–F) Quantification of total SCG volume (C), total CB volume (D), TH+ cell number (E) and TH+ cell density (F) on micrograph from HIF-2αWT(black dots, n = 4 for SCG and n = 6 for CB), TH-HIF-2αKO (red squares, n = 4), HIF-1αWT (black triangles, n = 4) and TH-HIF-1αKO (blue triangles, n = 3) mice. Data are expressed as mean ± SEM. Mann-Whitney test, **p<0.001; ns, non-significant. (G and H) TH-immunostained adrenal gland sections from HIF-2αWT(G, top panel), TH-HIF-2αKO (G, bottom panel), HIF-1αWT (H, top panel) and TH-HIF-1αKO (H, bottom panel) littermates. AM, adrenal medulla. Scale bars: 200 µm. (I) Normalized adrenaline (left) and noradrenaline (right) urine content measured by ELISA. HIF-2αWT(black dots, n = 8), TH-HIF-2αKO (red squares, n = 7), HIF-1αWT (black triangles, n = 7) and TH-HIF-1αKO (blue triangles, n = 4). Mann-Whitney test, ns, non-significant.

https://doi.org/10.7554/eLife.34681.002
Figure 1—figure supplement 1
Sympathoadrenal gene deletion by Th-IRES-Cre mouse strain.

(A) TH-Cre-mediated recombination in carotid bifurcation (left panels) and adrenal gland (right panels) sections of TH-activated tdTomato mice (Cre+, lower panels) compared to inactivated tdTomato (Cre-, upper panels) mice. Notice the presence of tdTomato fluorescence into the CB glomus cells, SCG sympathetic neurons and adrenal medulla due to TH-Cre activity (lower panels). Dashed lines delineate the location of SCG and AM within inactivated tdTomato (Cre-) sections. SCG, superior cervical ganglion; CB, carotid body; AM, adrenal medulla. Scale bars: 100 µm for carotid bifurcation and 200 µm for adrenal gland sections. (B–C) Relative Epas1 (Hif-2α) (B) and Hif1a (Hif-1α) (C) gene deletion of dissected SCG (left graphs) and AM (right graphs) from TH-HIF-2αKO (red, n = 4) and TH-HIF-1αKO (blue, n = 4) compared to their respective littermate controls (HIF-2αWT, n = 4; HIF-1αWT, n = 2). Data are expressed as mean ± SEM. Unpaired t-test, *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.

https://doi.org/10.7554/eLife.34681.003
Progressive CB glomus cells death during development of TH-HIF-2αKO mouse.

(A) Representative micrographs illustrating CB TH+ glomus cells appearance at embryo stage E18.5 (left) and postnatal stage P0 (right) in HIF-2αWT(top panels) and TH-HIF-2αKO (bottom panels) mice. Dashed rectangles (left panels) are shown at higher magnification on the right panels. SCG, superior cervical ganglion; CB, carotid body; ICA, internal carotid artery; ECA, external carotid artery. Scale bars: 100 µm. (B–E) Quantitative histological analysis of CB volume (B), TH+ cells number (C), TH+ cell density (D) and SCG volume (E) from TH-HIF-2αKO compared to HIF-2αWTmice. HIF-2αWT(E18.5, n = 8; P0, n = 4; SCG, n = 5), TH-HIF-2αKO (E18.5, n = 7; P0, n = 5; SCG, n = 5). SCG, superior cervical ganglion. Data are expressed as mean ±SEM. Two-way ANOVA, *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001, ns, non significant. (F) Representative pictures of double TH+ and TUNEL+ (white arrows) stained carotid bifurcation sections from HIF-2αWT(top panels) and TH-HIF-2αKO (bottom panels) mice at E18.5 (left) and P0 (right) stages. (G) Number of TUNEL+ cells within the CB (TH+ area) of HIF-2αWT(E18.5, n = 9; P0, n = 5) and TH-HIF-2αKO (E18.5, n = 5; P0, n = 4) mice at E18.5 and P0 stages. Data are expressed as mean ±SEM. Two-way ANOVA, *p<0.05, **p<0.01, ****p<0.0001. Scale bars: 50 µm.

https://doi.org/10.7554/eLife.34681.004
Figure 3 with 2 supplements
Effects of HIF-2α and HIF-1α sympathoadrenal loss on the HVR and whole-body metabolic activity in response to hypoxia.

(A and E) HVR in TH-HIF-2αKO (A, red line, n = 4) and TH-HIF-1αKO (E, blue line, n = 3) deficient mice compared to control HIF-2αWT(A, black line, n = 4) and HIF-1αWT (E, black line, n = 3) mice. Shift and duration of 10% O2 stimulus (30 min) are indicated. Shaded areas represent the period of time analysed in B and C or F and G, respectively. Data are presented as mean breaths/min every minute ±SEM. Two-way ANOVA, **p<0.01, ns, non-significant. (B and C) Averaged respiratory rate (B) and minute volume (C) of HIF-2αWT(black, n = 4) and TH-HIF-2αKO (red, n = 4) mice before and during the first 5 min of 10% O2 (shaded rectangle in A) or 5% CO2 exposure. Data are expressed as mean ±SEM. Two-way ANOVA, *p<0.05, ***p<0.001, ****p<0.0001, ns, non-significant. (D and H) Peripheral O2 saturation before, during and after 10% O2 (D) and 21% O2 (H) in HIF-2αWT(black, n = 8 in D, n = 4 in H) and TH-HIF-2αKO (red, n = 9 in D, n = 4 in H) mice. Data are expressed as mean percentage every 10 s ± SEM. Two-way ANOVA, ****p<0.0001. (F and G) Averaged respiratory rate (F) and minute volume (F) of HIF-1αWT (black, n = 3) and TH-HIF-1αKO (blue, n = 3) mice before and during the first 5 min of 10% O2 exposure (shaded rectangle in E). Data are expressed as mean ±SEM. Two-way ANOVA, *p<0.05, **p<0.01. (I–K) Baseline metabolic activity of HIF-2αWT(black, n = 3) and TH-HIF-2αKO (red, n = 3) mice. Data are presented as mean oxygen consumption (VO2, (I), carbon dioxide generation (VCO2, (J) and respiratory exchange ratio (RER, (K) every hour ±SEM. White and black boxes depict diurnal and nocturnal periods, respectively. Area under the curve followed by Mann-Whitney test, ns, non-significant. (L–N) Whole-body metabolic analysis of HIF-2αWT(black, n = 4) and TH-HIF-2αKO (red, n = 6) mice in response to 10% O2. Shift and duration of 10% O2 stimulus are indicated. Data are presented as mean oxygen consumption (VO2, (L), carbon dioxide generation (VCO2, (M) and respiratory exchange ratio (RER, (N) every hour ±SEM. White and black boxes depict diurnal and nocturnal periods, respectively. Recovery across the hypoxia period was analysed by one-phase association curve fitting. ****p<0.0001.

https://doi.org/10.7554/eLife.34681.005
Figure 3—figure supplement 1
Respiratory parameters of TH-HIF-2αKO and TH-HIF-1αKO mice exposed to acute hypoxia.

(A–J) Averaged tidal volume (A and F), inspiration time (B and G), expiration time (C and H), peak inspiratory flow (D and I) and peak expiratory flow (E and J) of TH-HIF-2αKO (n = 4) and TH-HIF-1αKO (n = 3) respect to control mice (HIF-2αWT, n = 4; HIF-1αWT, n = 3) before and during the first 5 min breathing 10% O2. Data are expressed as mean ±SEM. Two-way ANOVA, *p<0.05, **p<0.01, ***p<0.001.

https://doi.org/10.7554/eLife.34681.006
Figure 3—figure supplement 2
Secretory and electrophysiological properties in AM and SCG from TH-HIF-2αKO mice.

(A and B) Representative amperometric recordings of catecholamine release by chromaffin cells from HIF-2αWTand TH-HIF-2αKO mice (8–12 weeks old) in response to low PO2 (PO2 ≈ 10–15 mmHg), hypercapnia (20% CO2) and 20 mM KCl. (C) Percentage of AM slices with response to hypoxia, 20% CO2 and 20 mM KCl, respectively. HIF-2αWT n = 8; TH-HIF-2αKO, n = 7. (D) Averaged secretion rate of chromaffin cells from HIF-2αWTand TH-HIF-2αKO mice exposed to hypoxia (PO2 ≈ 10–15 mmHg), hypercapnia (20% CO2) and 20 mM KCl. Each data point represents the mean of 2–3 recordings per mouse. HIF-2αWT, n = 8; TH-HIF-2αKO, n = 7. Data are expressed as mean ±SEM. One-way ANOVA, ns, non-significant. (E and F) Ca2+ and K+ current/voltage (I/V) curves of AM chromaffin cells (E) and SCG sympathetic neurons (F) dissociated from HIF-2αWT(n = 9 cells from three mice) and TH-HIF-2αKO (n = 10 cells from three mice) mice. Data are expressed as mean ±SEM. Area under the curve followed by unpaired t-test, ns, non-significant.

https://doi.org/10.7554/eLife.34681.007
Figure 4 with 2 supplements
Impaired acclimatisation to chronic hypoxia and severe pulmonary hypertension in mice lacking CBs.

(A) Kaplan-Meier survival curve of the indicated mice housed at 10% O2 up to 21 days. HIF-2αWT(n = 12), TH-HIF-2αKO (n = 11), HIF-1αWT (n = 8) and TH-HIF-1αKO (n = 8). ***p<0.001. (B and C) Haematocrit (B) and haemoglobin (C) levels of HIF-2αWT(black) and TH-HIF-2αKO (red) littermates kept in normoxia (21% O2) and after 21 days at 10% O2. In B, HIF-2αWT(21% O2, n = 6; 10% O2, n = 18), TH-HIF-2αKO (21% O2, n = 7; 10% O2, n = 8). In C, HIF-2αWT(21% O2, n = 5; 10% O2, n = 8), TH-HIF-2αKO (21% O2, n = 5; 10% O2, n = 7). Data are expressed as mean ± SEM. Two-way ANOVA, *p<0.05, ***p<0.001, ****p<0.0001, ns, non-significant. (D and F) Normalized heart (D) and spleen (F) weight of HIF-2αWT(black) and TH-HIF-2αKO (red) before and after 21 days in hypoxia (10% O2). In D, HIF-2αWT(21% O2, n = 16; 10% O2, n = 23), TH-HIF-2αKO (21% O2, n = 15; 10% O2, n = 13). In F, HIF-2αWT(21% O2, n = 5; 10% O2, n = 23), TH-HIF-2αKO (21% O2, n = 5; 10% O2, n = 13). Data are expressed as mean ± SEM. Two-way ANOVA, ****p<0.0001, ns, non-significant. (E and G) Hematoxylin and eosin staining of heart (E) and spleen (G) of HIF-2αWT(top panel) and TH-HIF-2αKO (bottom panel) after 21 days in hypoxia (10% O2). Scale bars: 500 μm in E and 100 μm in G. (H) Fulton index on hearts dissected from HIF-2αWT(black, 21% O2, n = 17; 10% O2, n = 23) and TH-HIF-2αKO (red, 21% O2, n = 15; 10% O2, n = 17) mice before and after 21 days in hypoxia (10% O2). Data are expressed as mean ± SEM. Two-way ANOVA, ****p<0.0001, ns, non-significant. RV, right ventricle. LV, left ventricle. (I) Right ventricular systolic pressure (RVSP) recorded on HIF-2αWT(black, 21% O2, n = 6; 10% O2, n = 7) and TH-HIF-2αKO (red, 21% O2, n = 5; 10% O2, n = 5) mice maintained in normoxia (21% O2) or hypoxia (10% O2) for 21 days. Data are expressed as mean ± SEM. Two-way ANOVA, **p<0.01, ***p<0.001, ****p<0.0001, ns, non-significant. (J and K) Lung peripheral vessels muscularization (J) and arterial medial thickness (K) in HIF-2αWTand TH-HIF-2αKO mice exposed to 10% O2 for 14 and/or 21 days. In H, HIF-2αWT(10% O2 14d, n = 4; 10% O2 21d, n = 3), TH-HIF-2αKO (10% O2 14d, n = 6; 10% O2 21d, n = 3). In I, HIF-2αWT(21% O2, n = 5; 10% O2 21d, n = 8), TH-HIF-2αKO (21% O2, n = 5; 10% O2 21d, n = 8). Data are expressed as mean ± SEM. Two-way ANOVA, *p<0.05, **p<0.01, ****p<0.0001, ns, non-significant.

https://doi.org/10.7554/eLife.34681.008
Figure 4—figure supplement 1
Impaired hypoxia-induced CB proliferation in TH-HIF-2αKO mice.

(A) Glial fibrillary acidic protein (GFAP) immunostaining to illustrate the presence of CB stem cells in carotid bifurcation of both HIF-2αWTand TH-HIF-2αKO mice. Scale bars: 50 µm. (B) Double TH+ BrdU+ immunofluorescence performed on carotid bifurcation sections from HIF-2αWT(top) and TH-HIF-2αKO (bottom) mice exposed to 10% O2 for 14 days. Dashed rectangles are shown at higher magnification on the right panels. Newly formed TH+ cells are indicated with white arrows. Scale bars: 200 µm (left pictures), 50 µm (right pictures). (C and D) Quantification of total CB volume (C, n = 4 per genotype and condition) and double BrdU+ TH+ cells number (D, n = 3 per genotype and condition) in HIF-2αWT(black) and TH-HIF-2αKO (red) mice maintained for 14 days in hypoxia (10% O2). Data are presented as mean ±SEM. Unpaired t-test, **p<0.01, ***p<0.001. (E–H) Platelets (E), lymphocytes (F), granulocytes (G) and monocytes (H) blood counts in HIF-2αWT(n = 5, black) and TH-HIF-2αKO (n = 4, red) mice maintained for 21 days in hypoxia (10% O2). Unpaired t-test, *p<0.05, ns, non-significant.

https://doi.org/10.7554/eLife.34681.009
Figure 4—figure supplement 2
Adaptation to hypoxia in TH-HIF-1αKO animals.

(A) Haematocrit levels of HIF-1αWT (black, 21% O2, n = 4; 10% O2, n = 8) and TH-HIF-1αKO (blue, 21% O2, n = 4; 10% O2, n = 8) mice housed at 21% O2 or after 21 days at 10% O2. Data are expressed as mean ±SEM. Two-way ANOVA, ****p<0.001, ns, non-significant. (B and C) Normalized heart (B) and spleen (C) weight of HIF-1αWT (black) and TH-HIF-1αKO (blue) mice before and after 21 days of hypoxia (10% O2) exposure. In B, HIF-1αWT, 21% O2, n = 9; 10% O2, n = 8; TH-HIF-1αKO, n = 9, per condition. In C, 21% O2, n = 4 per genotype; 10% O2, n = 5 per genotype. Data are expressed as mean ± SEM. Two-way ANOVA, *p<0.05, ns, non-significant. (D) Fulton index on hearts dissected from HIF-1αWT (black) and TH-HIF-1αKO (blue) mice before and after 21 days in hypoxia (10% O2). HIF-1αWT, 21% O2, n = 7; 10% O2, n = 8; TH-HIF-1αKO, n = 8, per condition. Data are expressed as mean ± SEM. Two-way ANOVA, ****p<0.0001, ns, non-significant. RV, right ventricle. LV, left ventricle.

https://doi.org/10.7554/eLife.34681.010
Figure 5 with 1 supplement
Effects of CB dysfunction on blood pressure regulation.

(A–C) Circadian variations in baseline systolic blood pressure (A, continued line), diastolic blood pressure (A, broken line), mean blood pressure (B) and heart rate (C) of HIF-2αWT(black, n = 10) and TH-HIF-2αKO (red, n = 8) littermates recorded by radiotelemetry. White and black boxes depict diurnal and nocturnal periods, respectively. Data are presented as averaged values every hour ±SEM. Area under the curve followed by unpaired t-test are shown. BP, blood pressure. HR, heart rate in beats per minute. (D–F) Mean blood pressure (D), heart rate (E) and subcutaneous temperature (F) alteration in response to hypoxia in radiotelemetry-implanted TH-HIF-2αKO (red, n = 5) compared to HIF-2αWT(black, n = 5). Shift and duration of 10% O2 are indicated in the graph. White and black boxes represent diurnal and nocturnal periods, respectively. Data are presented as averaged values every hour ±SEM. Recovery across the hypoxia period was analysed by one-phase association curve fitting. BP, blood pressure. HR, heart rate in beats per minute. (G) Schematic representation of the protocol followed in the Ang II-induced experimental hypertension model. (H–M) Mean blood pressure and heart rate recorded from HIF-2αWT(black, n = 8) and TH-HIF-2αKO (red, n = 8) mice after 7 days (H and K), 14 days (I and L) and 21 days (J and M) of Ang II infusion. White and black boxes depict diurnal and nocturnal periods, respectively. Data are presented as averaged values every hour ±SEM. Area under the curve followed by unpaired t-test are shown. BP, blood pressure. HR, heart rate in beats per minute.

https://doi.org/10.7554/eLife.34681.011
Figure 5—figure supplement 1
Cardiovascular homeostasis in response to hypoxia and Ang II-induced experimental hypertension.

(A and B) Circadian oscillations in subcutaneous temperature (A) and physical activity (B) of radiotelemetry-implanted HIF-2αWT(black, n = 10) and TH-HIF-2αKO (red, n = 8). White and black boxes depict diurnal and nocturnal periods, respectively. Data are presented as averaged values every hour ± SEM. Area under the curve followed by unpaired t-test are shown. (C and D) Systolic blood pressure (C) and diastolic blood pressure (D) alteration in response to hypoxia in TH-HIF-2αKO (red, n = 5) compared to HIF-2αWT(black, n = 5) measured by radiotelemetry. Shift and duration of 10% O2 are indicated in the graph. White and black boxes depict diurnal and nocturnal periods, respectively. Data are presented as averaged blood pressure values every hour ± SEM. Recovery across the hypoxia period was analysed by one-phase association curve fitting. (E) Physical activity recorded by radiotelemetry of HIF-2αWT(black, n = 5) and TH-HIF-2αKO (red, n = 5) littermates exposed to 10% O2 environment. Shift and duration of 10% O2 are indicated in the graph. White and black boxes depict diurnal and nocturnal periods, respectively. Data are presented as averaged blood pressure values every hour ± SEM. Area under the curve followed by unpaired t-test is shown. (F–Q) Circadian fluctuations in systolic blood pressure, diastolic blood pressure, subcutaneous temperature and physical activity of HIF-2αWT(black, n = 5) and TH-HIF-2αKO (red, n = 5) after 7 days (F–I), 14 days (J–M) and 21 days (N–Q) of Ang II infusion recorded by radiotelemetry. White and black boxes represent diurnal and nocturnal periods, respectively. Data are presented as averaged values every hour ± SEM. Area under the curve followed by unpaired t-test are shown. ns, non-significant.

https://doi.org/10.7554/eLife.34681.012
Figure 6 with 1 supplement
Exercise performance and glucose management in mice lacking CBs.

(A–D). Time course showing the increment in O2 consumption (A), increment in CO2 generation (B), respiratory exchange ratio (C) and increment in heat production (D) from HIF-2αWT(black, n = 8) and TH-HIF-2αKO (red, n = 10) mice during exertion on a treadmill. Mice were warmed up for 5 min (5 m/min) and then the speed was accelerated 2 m/min at 2.5 min intervals until exhaustion. Averaged measurements every 2.5 min intervals ± SEM are charted. Two-way ANOVA, *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001. RER, respiratory exchange ratio. (E) Running total time spent by HIF-2αWT(black, n = 8) and TH-HIF-2αKO (red, n = 10) mice to become exhausted. Data are expressed as mean ± SEM. Unpaired t-test. (F and G) Aerobic capacity (F) and power output (G) measured in HIF-2αWT(black, n = 8) mice compared to TH-HIF-2αKO (red, n = 10) mice when performing at VO2max. Data are expressed as mean ± SEM. Unpaired t-test. *p<0.05. (H and I) Plasma glucose (H) and lactate (I) levels of HIF-2αWT(black, before, n = 7; after, n = 12) and TH-HIF-2αKO (black, before, n = 6; after, n = 12) littermates before and after running to exhaustion. Data are expressed as mean ± SEM. Two-way ANOVA, *p<0.05. ***p<0.001. ns, non-significant. (J and K) Plasma glucose levels of HIF-2αWT(black, n = 6) and TH-HIF-2αKO (red, n = 6) mice fed (J, n = 6 per genotype) or fasted over night (K, HIF-2αWT(n = 8) and TH-HIF-2αKO (n = 10). Data are expressed as mean ± SEM. Unpaired t-test. (L–M) Time courses showing the tolerance of HIF-2αWTand TH-HIF-2αKO mice to glucose (L, n = 7 per genotype) insulin (M, n = 11 per genotype) and lactate (N, n = 7 per genotype) injected bolus. Data are presented as mean ± SEM. Two-way ANOVA, *p<0.05, **p<0.01, ns, non-significant.

https://doi.org/10.7554/eLife.34681.013
Figure 6—figure supplement 1
Related to Figure 6.

Whole-body metabolic activity of TH-HIF-2αKO in response to fasting-induced hypoglycemia. (A–D) Oxygen consumption (A, VO2), carbon dioxide generation (B, VCO2), respiratory exchange rate (C) and heat production (D) of HIF-2αWT(black, n = 7) and TH-HIF-2αKO (red, n = 7) littermates under feed and over night fasting conditions. White and black boxes represent diurnal and nocturnal periods, respectively. Data are presented as averaged values every hour ± SEM. Area under the curve followed by unpaired t-test are shown. ns, non-significant.

https://doi.org/10.7554/eLife.34681.014
Figure 7 with 1 supplement
mTORC1 activation in CB development and hypoxia-induced CB neurogenesis.

(A) Double TH and p-S6 (mTORC1 activation marker) immunofluorescence on adult wild type CB slices to illustrate the increased p-S6 expression after 14 days in hypoxia (10% O2). For clarity, bottom panels only show p-S6 staining. TH+ outlined area (top panels) indicates the region used for pixels quantification. Scale bars: 50 µm. (B) Quantification of p-S6 (top) and TH (bottom) mean pixels intensity within the CB TH+ cells of wild type mice breathing 21% O2 or 10% O2 for 14 days. Each data point depicts the average of 3–4 pictures. 21% O2, n = 5; 10% O2 14d, n = 9 per genotype. Data are presented as mean ± SEM. Unpaired t-test, *p<0.05. (C) Representative micrographs of TH and p-S6 double immunostaining of HIF-2αWTand TH-HIF-2αKO embryonic (E18.5) carotid bifurcations. TH+ outlined area indicates the region used for pixels quantification. Scale bars: 50 µm. (D) Quantitative analysis performed on HIF-2αWT(black, n = 12) and TH-HIF-2αKO (red, n = 10) micrographs previously immuno-stained for p-S6 and TH. Each data point depicts the average of 3–4 pictures. Data are presented as mean ± SEM. Unpaired t-test, **p<0.01. (E) Double BrdU and TH immunofluorescence on carotid bifurcation sections from wild type mice (left and central panels) or TH-HIF-2αKO mice (right panel) exposed to 10% O2 and injected with rapamycin or vehicle control for 14 days. Notice the striking decrease in double BrdU+ TH+ cells (white arrowheads) in the rapamycin treated wild type mice compared to vehicle control animals. Scale bars: 100 µm. (F–H) Quantification of total CB volume (F), TH+ cells number (G) and percentage of double BrdU+ TH+ over the total TH+ cells (H) in wild type mice (black) or TH-HIF-2αKO mice (red) breathing 10% O2 and injected with rapamycin or vehicle control for 14 days. Wild type, n = 5 mice per treatment. TH-HIF-2αKO, n = 3. (I) Averaged breaths per minute during the first 2 min of acute hypoxia (10% O2) exposure from vehicle or rapamycin injected wild type mice (black) or TH-HIF-2αKO (red) mice before and after 7 days of chronic hypoxia (10% O2) treatment. Wild type, n = 14 mice per condition and treatment. TH-HIF-2αKO, n = 3. Data are presented as mean ± SEM. B, D, F, G and H, unpaired t-test, *p<0.05, ****p<0.0001. I, two-way ANOVA followed by Tukey’s multiple comparison test. ****p<0.0001, ns, non-significant.

https://doi.org/10.7554/eLife.34681.015
Figure 7—figure supplement 1
mTORC1 activity in SCG TH+ sympathetic neurons and effect of rapamycin treatment.

(A) Double TH and p-S6 (mTORC1 activation marker) immunofluorescence on adult wild type SCG slices after 14 days in hypoxia (10% O2). TH+ outlined area indicates the region used for pixels quantification. Scale bars: 100 µm. SCG, superior cervical ganglion. (B) Quantification of p-S6 (red) and TH (green) mean pixels intensity within the SCG TH+ area of wild type mice breathing 21% O2 or 10% O2 for 14 days. Each data point depicts the average of 3–4 pictures. 21% O2, n = 3; 10% O2, n = 4. Data are presented as mean ± SEM. Unpaired t-test, ns, non-significant. (C) Representative micrographs of TH and p-S6 double immunostaining of HIF-2αWTand TH-HIF-2αKO embryonic (E18.5) carotid bifurcations. SCG TH+ outlined area indicates the region used for pixels quantification. SCG, superior cervical ganglion. Scale bars: 100 µm. (D) Quantitative analysis performed on HIF-2αWT (black) and TH-HIF-2αKO (red) micrographs previously immune-stained for TH (green) and p-S6 (red). Each data point depicts the average of 3–4 pictures. 21% O2, n = 12; 10% O2, n = 10. Data are presented as mean ± SEM. Unpaired t-test, ns, non-significant. (E) Double TH and p-S6 immunofluorescence of vehicle control or rapamycin injected adult wild type SCG slices after 14 days breathing in a 10% O2 atmosphere. Notice the absence of p-S6 signal as a consequence of mTORC inhibition by rapamycin. SCG, superior cervical ganglion. CB, carotid body. Scale bars: 100 µm. (F) Haematocrit levels of vehicle control (n = 14) and rapamycin (n = 14) injected mice after 7 days at 10% O2. Un-paired t-test, ns, non-significant. (G) TH immunofluorescence of the carotid bifurcation of wild type mice injected for 14 days with vehicle control or rapamycin breathing room air. SCG, superior cervical ganglion. CB, carotid body. Scale bars: 100 µm. (H) Quantitative analysis of the CB parenchyma volume (top) and TH+ cell number (bottom) of wild type mice injected for 14 days with vehicle control or rapamycin and maintained in normoxic (21% O2) conditions.

https://doi.org/10.7554/eLife.34681.016
Graphic abstract of the role of HIF-2α in CB development and function.

(A) Schematic representation of a CB glomerulus. In CB development mTORC1 activity is high, which likely contributes to normal CB proliferation and growth. (B) Embryonic Epas1 (Hif-2α) ablation in TH+ cells (type I cells) leads to repressed mTORC1 activity and progressive O2-sensitive cell loss via a direct or indirect mechanism. (C) Upon low arterial pO2, CB O2-sensitive glomus cells trigger an acute hypoxic ventilatory response (HVR) increasing O2 uptake by the lungs. Sustained hypoxia induces CB growth, a process that is HIF-2α-dependent (Hodson et al., 2016) and blocked by rapamycin (mTORC1 inhibitor). Hypoxia-induced CB neurogenesis further increases ventilation and regulates cardiovascular function allowing adaptation. (D) The absence of CB responses to low pO2 leads to a more severe hypoxaemia, resulting in pathological polycythaemia, pulmonary hypertension, and right ventricular failure. Other adaptive responses, such as arterial pressure, exercise performance and glucose homeostasis, are also impaired by CB loss. Taken together, we show that HIF-2α is essential for CB development and that its absence results in the disruption of key homeostatic adaptive responses.

https://doi.org/10.7554/eLife.34681.017
Author response image 1
CB glomus cells identification by serotonin expression.

Double serotonin (5-HT, red) and TH (green) immunofluorescence on carotid bifurcations from HIF-2αWT and TH-HIF-2αKO mice at E18.5. Scale bars: 100 µm.

https://doi.org/10.7554/eLife.34681.020
Author response image 2
Histological analysis of the nucleus of the solitary tract.

NeuN immunohistochemistry of brain slices from HIF-2αWT andTH-HIF-2αKO mice. Left picture was obtained from Allen brain atlas (http://mouse.brain-map.org/static/atlas). Nucleus of the solitary tract is highlighted in purple. Dash line depicts the area corresponding with the nucleus of the solitary tract. Scale bars: 500 µm.

https://doi.org/10.7554/eLife.34681.021

Tables

Key resources table
Reagent type (species)
or resource
DesignationSource or referenceIdentifiersAdditional information
Gene (Mus musculus)Hif1aNAMGI:106918
Gene (M. musculus)Epas1NAMGI:109169
Gene (M. musculus)ThNAMGI:98735
Strain, strain background (M. musculus)C57BL/6JThe Jackson laboratoryJax:000664
Genetic reagent (M. musculus)HIF-1αWTPMID:10945599Jax: 007561
Genetic reagent (M. musculus)HIF-2αWTPMID:17284606Jax:008407
Genetic reagent (M. musculus)TH-CrePMID:15452869MGI:3056580
Genetic reagent (M. musculus)Td-TomatoPMID:20023653Jax:007909
Antibodyanti-TH (rabbit polyclonal)Novus BiologicalsNovus Biologicals:NB300-109(1:1000)
Antibodyanti-TH (chicken polyclonal)abcamabcam:ab76442(1:1000)
Antibodyanti-GFAP (rabbit polyclonal)DakoDako:Z0334(1:500)
Antibodyanti-BrdU (rat polyclonal)abcamabcam:ab6326(1:100)
Antibodyanti-phospho S6 (rabbit polyclonal)Cell Signaling TechnologyCell signaling:2211(1:200)
Antibodyanti-SMAα(mouse monoclonal)Sigma-AldrichSigma-Aldrich:A-2547(1:200)
AntibodyAlexa 488- or 568- secondariesThermoFisher(1:500)
Sequence-based reagentHif1a_probeIDT5’-/56-FAM/CCTGTTGGTTGCGCAGCAAGCATT/3BHQ_1/–3’
Sequence-based reagentHif1a_FIDT5’-GGTGCTGGTGTCCAAAATGTAG-3’
Sequence-based reagentHif1a_RIDT5’-ATGGGTCTAGAGAGATAGCTCCACA-3’
Sequence-based reagentEpas1_probeIDT5’-/56-FAM/CCACCTGGA/ZEN/CAAAGCCTCCATCAT/3IABkFQ/−3’
Sequence-based reagentEpas1_FIDT5’-TCTATGAGTTGGCTCATGAGTTG-3’
Sequence-based reagentEpas1_RIDT5’-GTCCGAAGGAAGCTGATGG-3’
Peptide, recombinant proteinAngIISigma-AldrichSigma-Aldrich:A2900
Peptide, recombinant proteinInsulin (human)Sigma-AldrichSigma-Aldrich:11 376 497 001
Peptide, recombinant proteinCollagenase type IASigma-AldrichSigma-Aldrich:C9891
Peptide, recombinant proteinTrypsinSigma-AldrichSigma-Aldrich:93610
Commercial assay or kitLSAB+, Dako REAL Detection SystemsDakoDako:K5001
Commercial assay or kitEpinephrine/Norepinephrine ELISA KitAbnovaAbnova:KA1877
Commercial assay or kitDNeasy Blood and Tissue KitQiagenQiagen:69506
Commercial assay or kitTaqMan Universal PCR Master MixApplied BiosystemsApplied biosystems:4304437
Commercial assay or kitClick-iT TUNEL Alexa Fluor 488 Imaging AssayThermoFisherThermoFisher:C10245
Chemical compound, drugBrdUSigma-AldrichSigma-Aldrich:B5002
Chemical compound, drugRapamycinLC LaboratoriesLC Laboratories:R-5000
Chemical compound, drugD-GlucoseSigma-AldrichSigma-Aldrich:G8270
Chemical compound, drugSodium L-LactateSigma-AldrichSigma-Aldrich:71718
Software, algorithmFijihttp://imagej.net/Fiji
OtherEVG stainMerckMerck:115974
OtherHematoxylin Solution, Mayer’sSigma-AldrichSigma-Aldrich:MHS16
OtherEosin Y solution, aqueousSigma-AldrichSigma-Aldrich:HT110216
OtherDAPI stainMolecular probesMolecular probes:D1306(1:5000)

Additional files

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. David Macias
  2. Andrew S Cowburn
  3. Hortensia Torres-Torrelo
  4. Patricia Ortega-Sáenz
  5. José López-Barneo
  6. Randall S Johnson
(2018)
HIF-2α is essential for carotid body development and function
eLife 7:e34681.
https://doi.org/10.7554/eLife.34681